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	<id>https://www.wikidoc.org/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Shivali+Marketkar</id>
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	<updated>2026-04-10T16:06:20Z</updated>
	<subtitle>User contributions</subtitle>
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	<entry>
		<id>https://www.wikidoc.org/index.php?title=File:800px-Mixed_germ_cell_tumour_-_intermed_mag.jpg&amp;diff=869034</id>
		<title>File:800px-Mixed germ cell tumour - intermed mag.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=File:800px-Mixed_germ_cell_tumour_-_intermed_mag.jpg&amp;diff=869034"/>
		<updated>2013-04-10T19:03:49Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=File:800px-Mixed_germ_cell_tumour_-_high_mag.jpg&amp;diff=869031</id>
		<title>File:800px-Mixed germ cell tumour - high mag.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=File:800px-Mixed_germ_cell_tumour_-_high_mag.jpg&amp;diff=869031"/>
		<updated>2013-04-10T18:58:38Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=File:400px-Enchondroma_-_very_high_mag.jpg&amp;diff=868991</id>
		<title>File:400px-Enchondroma - very high mag.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=File:400px-Enchondroma_-_very_high_mag.jpg&amp;diff=868991"/>
		<updated>2013-04-10T18:26:17Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Embryonal_carcinoma_pathophysiology&amp;diff=868982</id>
		<title>Embryonal carcinoma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Embryonal_carcinoma_pathophysiology&amp;diff=868982"/>
		<updated>2013-04-10T18:20:09Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Embryonal carcinoma}}&lt;br /&gt;
{{CMG}};{{AE}}{{SM}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
===Gross Pathology===&lt;br /&gt;
[[Image:Embryonal carcinoma - high mag.jpg|thumb|right|Embryonal carcinoma. [[H&amp;amp;E stain]].]]&lt;br /&gt;
The [[gross examination]] usually shows a two to three centimetre pale grey, poorly defined tumour with associated [[haemorrhage]] and [[necrosis]].&amp;lt;ref name=Robbins&amp;gt;{{cite book|last=Abbas, Fausto, Mitchell|title=Basic Pathology|year=2010|publisher=Elsevier|isbn=978-81-312-1036-9|pages=696–697}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Microscopic Pathology===&lt;br /&gt;
The microscopic features include: indistinct cell borders, mitoses, a variable architecture (tubulopapillary, glandular, solid, embryoid bodies - ball of cells surrounded by empty space on three sides), nuclear overlap, and necrosis. An important key to distinguish it from other tumors, such as seminoma (vacuolated), [[teratocarcinoma]] (3 differentiated germ layers), [[yolk sac tumor]] ([[Schiller-Duval bodies]]), and the [[Sertoli-Leydig cell tumor]] (strings of glands), is that the embryonal carcinoma cells are &amp;quot;trying&amp;quot; to evolve into their next stage of development. So in the testicle, they are often observed as blue cells attempting to form primitive tubules.&amp;lt;ref&amp;gt;http://library.med.utah.edu/WebPath/MALEHTML/MALE092.html&amp;lt;/ref&amp;gt;&lt;br /&gt;
Shown below is an image of embronal carcinoma(H&amp;amp;E stain).&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Embryonal_carcinoma_-_high_mag.jpg‎|400px|center]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
High magnification micrograph of an embryonal carcinoma, a type of germ cell tumour. &lt;br /&gt;
&lt;br /&gt;
Main features:&lt;br /&gt;
#Nuclear atypia.&lt;br /&gt;
#Nucleoli prominent.&lt;br /&gt;
#Necrosis common.&lt;br /&gt;
#Nuclei overlap.&lt;br /&gt;
&lt;br /&gt;
Other features:&lt;br /&gt;
&lt;br /&gt;
#Variable architecture: &lt;br /&gt;
#Tubulopapillary.&lt;br /&gt;
#Glandular.&lt;br /&gt;
#Solid.&lt;br /&gt;
#Embryoid bodies - ball of cells in surrounded by empty space on three sides.&lt;br /&gt;
#Mitoses common.&lt;br /&gt;
&lt;br /&gt;
===Video===&lt;br /&gt;
{{#ev:youtube|Ot3QjXcFim4}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Endocrinology]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
[[Category:Gynecology]]&lt;br /&gt;
[[Category:Pediatrics]]&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Needs overview]]&lt;br /&gt;
&lt;br /&gt;
{{WikiDoc Help Menu}}&lt;br /&gt;
{{WikiDoc Sources}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Embryonal_carcinoma_pathophysiology&amp;diff=868981</id>
		<title>Embryonal carcinoma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Embryonal_carcinoma_pathophysiology&amp;diff=868981"/>
		<updated>2013-04-10T18:19:05Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Embryonal carcinoma}}&lt;br /&gt;
{{CMG}};{{AE}}{{SM}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
===Gross Pathology===&lt;br /&gt;
[[Image:Embryonal carcinoma - high mag.jpg|thumb|right|Embryonal carcinoma. [[H&amp;amp;E stain]].]]&lt;br /&gt;
The [[gross examination]] usually shows a two to three centimetre pale grey, poorly defined tumour with associated [[haemorrhage]] and [[necrosis]].&amp;lt;ref name=Robbins&amp;gt;{{cite book|last=Abbas, Fausto, Mitchell|title=Basic Pathology|year=2010|publisher=Elsevier|isbn=978-81-312-1036-9|pages=696–697}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Microscopic Pathology===&lt;br /&gt;
The microscopic features include: indistinct cell borders, mitoses, a variable architecture (tubulopapillary, glandular, solid, embryoid bodies - ball of cells surrounded by empty space on three sides), nuclear overlap, and necrosis. An important key to distinguish it from other tumors, such as seminoma (vacuolated), [[teratocarcinoma]] (3 differentiated germ layers), [[yolk sac tumor]] ([[Schiller-Duval bodies]]), and the [[Sertoli-Leydig cell tumor]] (strings of glands), is that the embryonal carcinoma cells are &amp;quot;trying&amp;quot; to evolve into their next stage of development. So in the testicle, they are often observed as blue cells attempting to form primitive tubules.&amp;lt;ref&amp;gt;http://library.med.utah.edu/WebPath/MALEHTML/MALE092.html&amp;lt;/ref&amp;gt;&lt;br /&gt;
Shown below is an image of embronal carcinoma(H&amp;amp;E stain).&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Embryonal_carcinoma_-_high_mag.jpg‎|400px|center]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
High magnification micrograph of an embryonal carcinoma, a type of germ cell tumour. &lt;br /&gt;
&lt;br /&gt;
Main features:&lt;br /&gt;
Nuclear atypia.&lt;br /&gt;
Nucleoli prominent.&lt;br /&gt;
Necrosis common.&lt;br /&gt;
Nuclei overlap.&lt;br /&gt;
Other features:&lt;br /&gt;
&lt;br /&gt;
Variable architecture: &lt;br /&gt;
Tubulopapillary.&lt;br /&gt;
Glandular.&lt;br /&gt;
Solid.&lt;br /&gt;
Embryoid bodies - ball of cells in surrounded by empty space on three sides.&lt;br /&gt;
Mitoses common.&lt;br /&gt;
&lt;br /&gt;
===Video===&lt;br /&gt;
{{#ev:youtube|Ot3QjXcFim4}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Endocrinology]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
[[Category:Gynecology]]&lt;br /&gt;
[[Category:Pediatrics]]&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Needs overview]]&lt;br /&gt;
&lt;br /&gt;
{{WikiDoc Help Menu}}&lt;br /&gt;
{{WikiDoc Sources}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Embryonal_carcinoma_pathophysiology&amp;diff=868978</id>
		<title>Embryonal carcinoma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Embryonal_carcinoma_pathophysiology&amp;diff=868978"/>
		<updated>2013-04-10T18:18:26Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: /* Microscopic Pathology */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Embryonal carcinoma}}&lt;br /&gt;
{{CMG}};{{AE}}{{SM}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
===Gross Pathology===&lt;br /&gt;
[[Image:Embryonal carcinoma - high mag.jpg|thumb|right|Embryonal carcinoma. [[H&amp;amp;E stain]].]]&lt;br /&gt;
The [[gross examination]] usually shows a two to three centimetre pale grey, poorly defined tumour with associated [[haemorrhage]] and [[necrosis]].&amp;lt;ref name=Robbins&amp;gt;{{cite book|last=Abbas, Fausto, Mitchell|title=Basic Pathology|year=2010|publisher=Elsevier|isbn=978-81-312-1036-9|pages=696–697}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Microscopic Pathology===&lt;br /&gt;
The microscopic features include: indistinct cell borders, mitoses, a variable architecture (tubulopapillary, glandular, solid, embryoid bodies - ball of cells surrounded by empty space on three sides), nuclear overlap, and necrosis. An important key to distinguish it from other tumors, such as seminoma (vacuolated), [[teratocarcinoma]] (3 differentiated germ layers), [[yolk sac tumor]] ([[Schiller-Duval bodies]]), and the [[Sertoli-Leydig cell tumor]] (strings of glands), is that the embryonal carcinoma cells are &amp;quot;trying&amp;quot; to evolve into their next stage of development. So in the testicle, they are often observed as blue cells attempting to form primitive tubules.&amp;lt;ref&amp;gt;http://library.med.utah.edu/WebPath/MALEHTML/MALE092.html&amp;lt;/ref&amp;gt;&lt;br /&gt;
Shown below is an image of embronal carcinoma(H&amp;amp;E stain).&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Embryonal_carcinoma_-_high_mag.jpg‎|400px|center]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
High magnification micrograph of an embryonal carcinoma, a type of germ cell tumour. &lt;br /&gt;
Main features:&lt;br /&gt;
Nuclear atypia.&lt;br /&gt;
Nucleoli prominent.&lt;br /&gt;
Necrosis common.&lt;br /&gt;
Nuclei overlap.&lt;br /&gt;
Other features:&lt;br /&gt;
&lt;br /&gt;
Variable architecture: &lt;br /&gt;
Tubulopapillary.&lt;br /&gt;
Glandular.&lt;br /&gt;
Solid.&lt;br /&gt;
Embryoid bodies - ball of cells in surrounded by empty space on three sides.&lt;br /&gt;
Mitoses common.&lt;br /&gt;
&lt;br /&gt;
===Video===&lt;br /&gt;
{{#ev:youtube|Ot3QjXcFim4}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Endocrinology]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
[[Category:Gynecology]]&lt;br /&gt;
[[Category:Pediatrics]]&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Needs overview]]&lt;br /&gt;
&lt;br /&gt;
{{WikiDoc Help Menu}}&lt;br /&gt;
{{WikiDoc Sources}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Embryonal_carcinoma_pathophysiology&amp;diff=868973</id>
		<title>Embryonal carcinoma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Embryonal_carcinoma_pathophysiology&amp;diff=868973"/>
		<updated>2013-04-10T18:17:24Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Embryonal carcinoma}}&lt;br /&gt;
{{CMG}};{{AE}}{{SM}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
===Gross Pathology===&lt;br /&gt;
[[Image:Embryonal carcinoma - high mag.jpg|thumb|right|Embryonal carcinoma. [[H&amp;amp;E stain]].]]&lt;br /&gt;
The [[gross examination]] usually shows a two to three centimetre pale grey, poorly defined tumour with associated [[haemorrhage]] and [[necrosis]].&amp;lt;ref name=Robbins&amp;gt;{{cite book|last=Abbas, Fausto, Mitchell|title=Basic Pathology|year=2010|publisher=Elsevier|isbn=978-81-312-1036-9|pages=696–697}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Microscopic Pathology===&lt;br /&gt;
The microscopic features include: indistinct cell borders, mitoses, a variable architecture (tubulopapillary, glandular, solid, embryoid bodies - ball of cells surrounded by empty space on three sides), nuclear overlap, and necrosis. An important key to distinguish it from other tumors, such as seminoma (vacuolated), [[teratocarcinoma]] (3 differentiated germ layers), [[yolk sac tumor]] ([[Schiller-Duval bodies]]), and the [[Sertoli-Leydig cell tumor]] (strings of glands), is that the embryonal carcinoma cells are &amp;quot;trying&amp;quot; to evolve into their next stage of development. So in the testicle, they are often observed as blue cells attempting to form primitive tubules.&amp;lt;ref&amp;gt;http://library.med.utah.edu/WebPath/MALEHTML/MALE092.html&amp;lt;/ref&amp;gt;&lt;br /&gt;
Shown below is an image of embronal carcinoma(H&amp;amp;E stain).&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Embryonal_carcinoma_-_high_mag.jpg‎|400px|left]]&lt;br /&gt;
&lt;br /&gt;
The high magnification image shows:&lt;br /&gt;
High magnification micrograph of an embryonal carcinoma, a type of germ cell tumour. H&amp;amp;E stain. &lt;br /&gt;
Main features:&lt;br /&gt;
Nuclear atypia.&lt;br /&gt;
Nucleoli prominent.&lt;br /&gt;
Necrosis common.&lt;br /&gt;
Nuclei overlap.&lt;br /&gt;
Other features:&lt;br /&gt;
&lt;br /&gt;
Variable architecture: &lt;br /&gt;
Tubulopapillary.&lt;br /&gt;
Glandular.&lt;br /&gt;
Solid.&lt;br /&gt;
Embryoid bodies - ball of cells in surrounded by empty space on three sides.&lt;br /&gt;
Mitoses common.&lt;br /&gt;
&lt;br /&gt;
===Video===&lt;br /&gt;
{{#ev:youtube|Ot3QjXcFim4}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Endocrinology]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
[[Category:Gynecology]]&lt;br /&gt;
[[Category:Pediatrics]]&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Needs overview]]&lt;br /&gt;
&lt;br /&gt;
{{WikiDoc Help Menu}}&lt;br /&gt;
{{WikiDoc Sources}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Embryonal_carcinoma_pathophysiology&amp;diff=868968</id>
		<title>Embryonal carcinoma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Embryonal_carcinoma_pathophysiology&amp;diff=868968"/>
		<updated>2013-04-10T18:16:48Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Embryonal carcinoma}}&lt;br /&gt;
{{CMG}};{{AE}}{{SM}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
===Gross Pathology===&lt;br /&gt;
[[Image:Embryonal carcinoma - high mag.jpg|thumb|right|Embryonal carcinoma. [[H&amp;amp;E stain]].]]&lt;br /&gt;
The [[gross examination]] usually shows a two to three centimetre pale grey, poorly defined tumour with associated [[haemorrhage]] and [[necrosis]].&amp;lt;ref name=Robbins&amp;gt;{{cite book|last=Abbas, Fausto, Mitchell|title=Basic Pathology|year=2010|publisher=Elsevier|isbn=978-81-312-1036-9|pages=696–697}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Microscopic Pathology===&lt;br /&gt;
The microscopic features include: indistinct cell borders, mitoses, a variable architecture (tubulopapillary, glandular, solid, embryoid bodies - ball of cells surrounded by empty space on three sides), nuclear overlap, and necrosis. An important key to distinguish it from other tumors, such as seminoma (vacuolated), [[teratocarcinoma]] (3 differentiated germ layers), [[yolk sac tumor]] ([[Schiller-Duval bodies]]), and the [[Sertoli-Leydig cell tumor]] (strings of glands), is that the embryonal carcinoma cells are &amp;quot;trying&amp;quot; to evolve into their next stage of development. So in the testicle, they are often observed as blue cells attempting to form primitive tubules.&amp;lt;ref&amp;gt;http://library.med.utah.edu/WebPath/MALEHTML/MALE092.html&amp;lt;/ref&amp;gt;&lt;br /&gt;
Shown below is an image of embronal carcinoma(H&amp;amp;E stain).&lt;br /&gt;
[[Image:800px-Embryonal_carcinoma_-_high_mag.jpg‎|400px|left]]&lt;br /&gt;
&lt;br /&gt;
The high magnification image shows:&lt;br /&gt;
High magnification micrograph of an embryonal carcinoma, a type of germ cell tumour. H&amp;amp;E stain. &lt;br /&gt;
Main features:&lt;br /&gt;
Nuclear atypia.&lt;br /&gt;
Nucleoli prominent.&lt;br /&gt;
Necrosis common.&lt;br /&gt;
Nuclei overlap.&lt;br /&gt;
Other features:&lt;br /&gt;
&lt;br /&gt;
Variable architecture: &lt;br /&gt;
Tubulopapillary.&lt;br /&gt;
Glandular.&lt;br /&gt;
Solid.&lt;br /&gt;
Embryoid bodies - ball of cells in surrounded by empty space on three sides.&lt;br /&gt;
Mitoses common.&lt;br /&gt;
&lt;br /&gt;
===Video===&lt;br /&gt;
{{#ev:youtube|Ot3QjXcFim4}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Endocrinology]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
[[Category:Gynecology]]&lt;br /&gt;
[[Category:Pediatrics]]&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Needs overview]]&lt;br /&gt;
&lt;br /&gt;
{{WikiDoc Help Menu}}&lt;br /&gt;
{{WikiDoc Sources}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Embryonal_carcinoma_pathophysiology&amp;diff=868963</id>
		<title>Embryonal carcinoma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Embryonal_carcinoma_pathophysiology&amp;diff=868963"/>
		<updated>2013-04-10T18:15:45Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Embryonal carcinoma}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
===Gross Pathology===&lt;br /&gt;
[[Image:Embryonal carcinoma - high mag.jpg|thumb|right|Embryonal carcinoma. [[H&amp;amp;E stain]].]]&lt;br /&gt;
The [[gross examination]] usually shows a two to three centimetre pale grey, poorly defined tumour with associated [[haemorrhage]] and [[necrosis]].&amp;lt;ref name=Robbins&amp;gt;{{cite book|last=Abbas, Fausto, Mitchell|title=Basic Pathology|year=2010|publisher=Elsevier|isbn=978-81-312-1036-9|pages=696–697}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Microscopic Pathology===&lt;br /&gt;
The microscopic features include: indistinct cell borders, mitoses, a variable architecture (tubulopapillary, glandular, solid, embryoid bodies - ball of cells surrounded by empty space on three sides), nuclear overlap, and necrosis. An important key to distinguish it from other tumors, such as seminoma (vacuolated), [[teratocarcinoma]] (3 differentiated germ layers), [[yolk sac tumor]] ([[Schiller-Duval bodies]]), and the [[Sertoli-Leydig cell tumor]] (strings of glands), is that the embryonal carcinoma cells are &amp;quot;trying&amp;quot; to evolve into their next stage of development. So in the testicle, they are often observed as blue cells attempting to form primitive tubules.&amp;lt;ref&amp;gt;http://library.med.utah.edu/WebPath/MALEHTML/MALE092.html&amp;lt;/ref&amp;gt;&lt;br /&gt;
Shown below is an image of embronal carcinoma(H&amp;amp;E stain).&lt;br /&gt;
[[Image:800px-Embryonal_carcinoma_-_high_mag.jpg‎|200px|center]]&lt;br /&gt;
&lt;br /&gt;
The high magnification image shows:&lt;br /&gt;
High magnification micrograph of an embryonal carcinoma, a type of germ cell tumour. H&amp;amp;E stain. &lt;br /&gt;
Main features:&lt;br /&gt;
Nuclear atypia.&lt;br /&gt;
Nucleoli prominent.&lt;br /&gt;
Necrosis common.&lt;br /&gt;
Nuclei overlap.&lt;br /&gt;
Other features:&lt;br /&gt;
&lt;br /&gt;
Variable architecture: &lt;br /&gt;
Tubulopapillary.&lt;br /&gt;
Glandular.&lt;br /&gt;
Solid.&lt;br /&gt;
Embryoid bodies - ball of cells in surrounded by empty space on three sides.&lt;br /&gt;
Mitoses common.&lt;br /&gt;
===Video===&lt;br /&gt;
{{#ev:youtube|Ot3QjXcFim4}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Endocrinology]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
[[Category:Gynecology]]&lt;br /&gt;
[[Category:Pediatrics]]&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Needs overview]]&lt;br /&gt;
&lt;br /&gt;
{{WikiDoc Help Menu}}&lt;br /&gt;
{{WikiDoc Sources}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=File:800px-Embryonal_carcinoma_-_high_mag.jpg&amp;diff=868958</id>
		<title>File:800px-Embryonal carcinoma - high mag.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=File:800px-Embryonal_carcinoma_-_high_mag.jpg&amp;diff=868958"/>
		<updated>2013-04-10T18:11:42Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=File:Lossy-page1-751px-Elastofibroma_stained_with_elastic_stain_LDRT_tif.jpg&amp;diff=868915</id>
		<title>File:Lossy-page1-751px-Elastofibroma stained with elastic stain LDRT tif.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=File:Lossy-page1-751px-Elastofibroma_stained_with_elastic_stain_LDRT_tif.jpg&amp;diff=868915"/>
		<updated>2013-04-10T17:37:02Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=File:Lossy-page1-751px-Hematoxylin_and_Eosin_stained_photomicrograph_of_an_elastofibroma_LDRT_tif.jpg&amp;diff=868872</id>
		<title>File:Lossy-page1-751px-Hematoxylin and Eosin stained photomicrograph of an elastofibroma LDRT tif.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=File:Lossy-page1-751px-Hematoxylin_and_Eosin_stained_photomicrograph_of_an_elastofibroma_LDRT_tif.jpg&amp;diff=868872"/>
		<updated>2013-04-10T16:03:39Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Dysplastic_nevus_pathophysiology&amp;diff=868867</id>
		<title>Dysplastic nevus pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Dysplastic_nevus_pathophysiology&amp;diff=868867"/>
		<updated>2013-04-10T15:57:33Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Dysplastic nevus}}&lt;br /&gt;
{{CMG}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
===Microscopy===&lt;br /&gt;
Most dermatologists and dermatopathologists use a system devised by the [[NIH]] for classifying melanocytic lesions.  In this classification, a nevus can be defined as benign, having atypia, or being a melanoma.  A benign nevus is read as (or understood as) having no cytologic or architectural atypia.  An atypical mole is read as having architectural atypia, and having (mild, moderate, or severe) cytologic (melanocytic) atypia.&amp;lt;ref&amp;gt;http://www.labpath.com/new1.html&amp;lt;/ref&amp;gt;  Usually, cytologic atypia is of more important clinical concern than architectural atypia.  Usually, moderate to severe cytologic atypia will require further excision to make sure that the surgical margin is completely clear of the lesion.  {{Citation needed|date=July 2011}}&lt;br /&gt;
&lt;br /&gt;
The most important aspect of the biopsy report is that the pathologist indicates if the margin is clear (negative or free of melanocytic nevus), or if further tissue (a second surgery) is required.  If this is not mentioned, usually a dermatologist or clinician will require further surgery if moderate to severe cytologic atypia is present - and if residual nevus is present at the surgical margin.&lt;br /&gt;
&lt;br /&gt;
===Associated conditions===&lt;br /&gt;
;Atypical Mole Syndrome&lt;br /&gt;
Atypical Mole Syndrome is a hereditary condition which causes the person to have a large quantity of moles (often 100 or more) with some dysplastic nevi.  This often leads to a higher [[risk]] of [[melanoma]], a serious [[skin cancer]].&amp;lt;ref&amp;gt;Burkhart, C.G MPH, MD. Dysplastic nevus declassified; even the NIH recommends elimination of confusing terminology. SKINmed: Dermatology for the Clinician 2(1):12-13, 2003.&amp;lt;/ref&amp;gt;&lt;br /&gt;
A slight majority of melanomas do &#039;&#039;not&#039;&#039; form in an existing mole, but rather create a new [[growth]] on the skin. Nevertheless, those with more dysplastic nevi are at a higher risk of this type of melanoma occurrence.&amp;lt;ref&amp;gt;D.J. Pope, T. Sorahan, J.R. Marsden, P.M. Ball, R.P. Grimley and I.M. Peck. Benign pigmented nevi in children. Arch of Dermatology 2006;142:1599-1604&amp;lt;/ref&amp;gt;&amp;lt;ref&amp;gt;D.E. Goldgar, L.A. Cannon-Albright, L.J. Meyer, M.W. Pipekorn, J.J. Zone, M.H. Skolnick. Inheritance of Nevus Number and Size in Melanoma and Dysplastic Nevus Syndrome Kindreds. Journal of the National Cancer Institute 1991 83(23):1726-1733&amp;lt;/ref&amp;gt; Such persons need to be checked regularly for any changes in their moles and to note any new ones.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Video===&lt;br /&gt;
{{#ev:youtube|kpHHtp05ba8}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
{{WH}}&lt;br /&gt;
{{WS}}&lt;br /&gt;
[[Category:Needs Overview]]&lt;br /&gt;
[[Category:Needs Content]]&lt;br /&gt;
[[Category:Dermatology]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Dysplastic_nevus_pathophysiology&amp;diff=868866</id>
		<title>Dysplastic nevus pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Dysplastic_nevus_pathophysiology&amp;diff=868866"/>
		<updated>2013-04-10T15:57:09Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Dysplastic nevus}}&lt;br /&gt;
{{CMG}}&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
===Microscopy===&lt;br /&gt;
Most dermatologists and dermatopathologists use a system devised by the [[NIH]] for classifying melanocytic lesions.  In this classification, a nevus can be defined as benign, having atypia, or being a melanoma.  A benign nevus is read as (or understood as) having no cytologic or architectural atypia.  An atypical mole is read as having architectural atypia, and having (mild, moderate, or severe) cytologic (melanocytic) atypia.&amp;lt;ref&amp;gt;http://www.labpath.com/new1.html&amp;lt;/ref&amp;gt;  Usually, cytologic atypia is of more important clinical concern than architectural atypia.  Usually, moderate to severe cytologic atypia will require further excision to make sure that the surgical margin is completely clear of the lesion.  {{Citation needed|date=July 2011}}&lt;br /&gt;
&lt;br /&gt;
The most important aspect of the biopsy report is that the pathologist indicates if the margin is clear (negative or free of melanocytic nevus), or if further tissue (a second surgery) is required.  If this is not mentioned, usually a dermatologist or clinician will require further surgery if moderate to severe cytologic atypia is present - and if residual nevus is present at the surgical margin.&lt;br /&gt;
&lt;br /&gt;
===Associated conditions===&lt;br /&gt;
;Atypical Mole Syndrome&lt;br /&gt;
Atypical Mole Syndrome is a hereditary condition which causes the person to have a large quantity of moles (often 100 or more) with some dysplastic nevi.  This often leads to a higher [[risk]] of [[melanoma]], a serious [[skin cancer]].&amp;lt;ref&amp;gt;Burkhart, C.G MPH, MD. Dysplastic nevus declassified; even the NIH recommends elimination of confusing terminology. SKINmed: Dermatology for the Clinician 2(1):12-13, 2003.&amp;lt;/ref&amp;gt;&lt;br /&gt;
A slight majority of melanomas do &#039;&#039;not&#039;&#039; form in an existing mole, but rather create a new [[growth]] on the skin. Nevertheless, those with more dysplastic nevi are at a higher risk of this type of melanoma occurrence.&amp;lt;ref&amp;gt;D.J. Pope, T. Sorahan, J.R. Marsden, P.M. Ball, R.P. Grimley and I.M. Peck. Benign pigmented nevi in children. Arch of Dermatology 2006;142:1599-1604&amp;lt;/ref&amp;gt;&amp;lt;ref&amp;gt;D.E. Goldgar, L.A. Cannon-Albright, L.J. Meyer, M.W. Pipekorn, J.J. Zone, M.H. Skolnick. Inheritance of Nevus Number and Size in Melanoma and Dysplastic Nevus Syndrome Kindreds. Journal of the National Cancer Institute 1991 83(23):1726-1733&amp;lt;/ref&amp;gt; Such persons need to be checked regularly for any changes in their moles and to note any new ones.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Video===&lt;br /&gt;
{{#ev:youtube|kpHHtp05ba8}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
{{WH}}&lt;br /&gt;
{{WS}}&lt;br /&gt;
[[Category:Needs Overview]]&lt;br /&gt;
[[Category:Needs Content]]&lt;br /&gt;
[[Category:Dermatology]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Dysplastic_nevus_pathophysiology&amp;diff=868865</id>
		<title>Dysplastic nevus pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Dysplastic_nevus_pathophysiology&amp;diff=868865"/>
		<updated>2013-04-10T15:56:37Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Dysplastic nevus}}&lt;br /&gt;
{{CMG}}&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
===Microscopy===&lt;br /&gt;
Most dermatologists and dermatopathologists use a system devised by the [[NIH]] for classifying melanocytic lesions.  In this classification, a nevus can be defined as benign, having atypia, or being a melanoma.  A benign nevus is read as (or understood as) having no cytologic or architectural atypia.  An atypical mole is read as having architectural atypia, and having (mild, moderate, or severe) cytologic (melanocytic) atypia.&amp;lt;ref&amp;gt;http://www.labpath.com/new1.html&amp;lt;/ref&amp;gt;  Usually, cytologic atypia is of more important clinical concern than architectural atypia.  Usually, moderate to severe cytologic atypia will require further excision to make sure that the surgical margin is completely clear of the lesion.  {{Citation needed|date=July 2011}}&lt;br /&gt;
&lt;br /&gt;
The most important aspect of the biopsy report is that the pathologist indicates if the margin is clear (negative or free of melanocytic nevus), or if further tissue (a second surgery) is required.  If this is not mentioned, usually a dermatologist or clinician will require further surgery if moderate to severe cytologic atypia is present - and if residual nevus is present at the surgical margin.&lt;br /&gt;
&lt;br /&gt;
===Associated conditions===&lt;br /&gt;
;Atypical Mole Syndrome&lt;br /&gt;
Atypical Mole Syndrome is a hereditary condition which causes the person to have a large quantity of moles (often 100 or more) with some dysplastic nevi.  This often leads to a higher [[risk]] of [[melanoma]], a serious [[skin cancer]].&amp;lt;ref&amp;gt;Burkhart, C.G MPH, MD. Dysplastic nevus declassified; even the NIH recommends elimination of confusing terminology. SKINmed: Dermatology for the Clinician 2(1):12-13, 2003.&amp;lt;/ref&amp;gt;&lt;br /&gt;
A slight majority of melanomas do &#039;&#039;not&#039;&#039; form in an existing mole, but rather create a new [[growth]] on the skin. Nevertheless, those with more dysplastic nevi are at a higher risk of this type of melanoma occurrence.&amp;lt;ref&amp;gt;D.J. Pope, T. Sorahan, J.R. Marsden, P.M. Ball, R.P. Grimley and I.M. Peck. Benign pigmented nevi in children. Arch of Dermatology 2006;142:1599-1604&amp;lt;/ref&amp;gt;&amp;lt;ref&amp;gt;D.E. Goldgar, L.A. Cannon-Albright, L.J. Meyer, M.W. Pipekorn, J.J. Zone, M.H. Skolnick. Inheritance of Nevus Number and Size in Melanoma and Dysplastic Nevus Syndrome Kindreds. Journal of the National Cancer Institute 1991 83(23):1726-1733&amp;lt;/ref&amp;gt; Such persons need to be checked regularly for any changes in their moles and to note any new ones.&lt;br /&gt;
&lt;br /&gt;
===Video===&lt;br /&gt;
{{#ev:youtube|kpHHtp05ba8}}&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
{{WH}}&lt;br /&gt;
{{WS}}&lt;br /&gt;
[[Category:Needs Overview]]&lt;br /&gt;
[[Category:Needs Content]]&lt;br /&gt;
[[Category:Dermatology]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Dermatofibroma_pathophysiology&amp;diff=865953</id>
		<title>Dermatofibroma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Dermatofibroma_pathophysiology&amp;diff=865953"/>
		<updated>2013-04-01T14:49:51Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Dermatofibroma}}&lt;br /&gt;
{{CMG}};{{AE}}{{SM}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
* Some physicians and researchers believe dermatofibromas form as a reaction to previous injuries such as insect bites or thorn pricks.&lt;br /&gt;
* Dermatofibromas are composed of disordered [[collagen]] laid down by [[fibroblasts]].&lt;br /&gt;
&lt;br /&gt;
===Immunohistochemical staining===&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
!  Neoplasm&lt;br /&gt;
!  [[CD34]]&lt;br /&gt;
!  [[Stromelysin-3]]&amp;lt;ref&amp;gt;{{cite journal | pmid = 17596171 | doi=10.1111/j.1365-2133.2007.08033.x | volume=157 | issue=2 | title=Stromelysin-3 expression in the differential diagnosis of dermatofibroma and dermatofibrosarcoma protuberans: comparison with factor XIIIa and CD34 | year=2007 | month=August | author=Kim HJ, Lee JY, Kim SH, &#039;&#039;et al.&#039;&#039; | journal=Br. J. Dermatol. | pages=319–24}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
!  [[Factor XIIIa]]&amp;lt;ref&amp;gt;http://emedicine.medscape.com/article/1056742-overview&amp;lt;/ref&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|  Dermatofibroma&lt;br /&gt;
|  +&lt;br /&gt;
|  +&lt;br /&gt;
|  +&lt;br /&gt;
|-&lt;br /&gt;
|  [[Dermatofibrosarcoma protuberans]]&lt;br /&gt;
|  +&lt;br /&gt;
|  -&lt;br /&gt;
|  - &lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Video===&lt;br /&gt;
{{#ev:youtube|tq4xFLIw1TA}}&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&lt;br /&gt;
{{Reflist|2}}&lt;br /&gt;
[[Category:Needs overview]]&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Dermatology]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Oncology]]&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Dermatofibroma_pathophysiology&amp;diff=865952</id>
		<title>Dermatofibroma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Dermatofibroma_pathophysiology&amp;diff=865952"/>
		<updated>2013-04-01T14:49:12Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Dermatofibroma}}&lt;br /&gt;
{{CMG}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
* Some physicians and researchers believe dermatofibromas form as a reaction to previous injuries such as insect bites or thorn pricks.&lt;br /&gt;
* Dermatofibromas are composed of disordered [[collagen]] laid down by [[fibroblasts]].&lt;br /&gt;
&lt;br /&gt;
===Immunohistochemical staining===&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
!  Neoplasm&lt;br /&gt;
!  [[CD34]]&lt;br /&gt;
!  [[Stromelysin-3]]&amp;lt;ref&amp;gt;{{cite journal | pmid = 17596171 | doi=10.1111/j.1365-2133.2007.08033.x | volume=157 | issue=2 | title=Stromelysin-3 expression in the differential diagnosis of dermatofibroma and dermatofibrosarcoma protuberans: comparison with factor XIIIa and CD34 | year=2007 | month=August | author=Kim HJ, Lee JY, Kim SH, &#039;&#039;et al.&#039;&#039; | journal=Br. J. Dermatol. | pages=319–24}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
!  [[Factor XIIIa]]&amp;lt;ref&amp;gt;http://emedicine.medscape.com/article/1056742-overview&amp;lt;/ref&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|  Dermatofibroma&lt;br /&gt;
|  +&lt;br /&gt;
|  +&lt;br /&gt;
|  +&lt;br /&gt;
|-&lt;br /&gt;
|  [[Dermatofibrosarcoma protuberans]]&lt;br /&gt;
|  +&lt;br /&gt;
|  -&lt;br /&gt;
|  - &lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Video===&lt;br /&gt;
{{#ev:youtube|tq4xFLIw1TA}}&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&lt;br /&gt;
{{Reflist|2}}&lt;br /&gt;
[[Category:Needs overview]]&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Dermatology]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Oncology]]&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Dermatofibroma_pathophysiology&amp;diff=865951</id>
		<title>Dermatofibroma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Dermatofibroma_pathophysiology&amp;diff=865951"/>
		<updated>2013-04-01T14:48:43Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Dermatofibroma}}&lt;br /&gt;
{{CMG}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
* Some physicians and researchers believe dermatofibromas form as a reaction to previous injuries such as insect bites or thorn pricks.&lt;br /&gt;
* Dermatofibromas are composed of disordered [[collagen]] laid down by [[fibroblasts]].&lt;br /&gt;
&lt;br /&gt;
===Immunohistochemical staining===&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
!  Neoplasm&lt;br /&gt;
!  [[CD34]]&lt;br /&gt;
!  [[Stromelysin-3]]&amp;lt;ref&amp;gt;{{cite journal | pmid = 17596171 | doi=10.1111/j.1365-2133.2007.08033.x | volume=157 | issue=2 | title=Stromelysin-3 expression in the differential diagnosis of dermatofibroma and dermatofibrosarcoma protuberans: comparison with factor XIIIa and CD34 | year=2007 | month=August | author=Kim HJ, Lee JY, Kim SH, &#039;&#039;et al.&#039;&#039; | journal=Br. J. Dermatol. | pages=319–24}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
!  [[Factor XIIIa]]&amp;lt;ref&amp;gt;http://emedicine.medscape.com/article/1056742-overview&amp;lt;/ref&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|  Dermatofibroma&lt;br /&gt;
|  +&lt;br /&gt;
|  +&lt;br /&gt;
|  +&lt;br /&gt;
|-&lt;br /&gt;
|  [[Dermatofibrosarcoma protuberans]]&lt;br /&gt;
|  +&lt;br /&gt;
|  -&lt;br /&gt;
|  - &lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Video===&lt;br /&gt;
{{#ev:youtube|v=tq4xFLIw1TA}}&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&lt;br /&gt;
{{Reflist|2}}&lt;br /&gt;
[[Category:Needs overview]]&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Dermatology]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Oncology]]&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Dermatofibroma_pathophysiology&amp;diff=865950</id>
		<title>Dermatofibroma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Dermatofibroma_pathophysiology&amp;diff=865950"/>
		<updated>2013-04-01T14:46:05Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Dermatofibroma}}&lt;br /&gt;
{{CMG}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
* Some physicians and researchers believe dermatofibromas form as a reaction to previous injuries such as insect bites or thorn pricks.&lt;br /&gt;
* Dermatofibromas are composed of disordered [[collagen]] laid down by [[fibroblasts]].&lt;br /&gt;
&lt;br /&gt;
===Immunohistochemical staining===&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
!  Neoplasm&lt;br /&gt;
!  [[CD34]]&lt;br /&gt;
!  [[Stromelysin-3]]&amp;lt;ref&amp;gt;{{cite journal | pmid = 17596171 | doi=10.1111/j.1365-2133.2007.08033.x | volume=157 | issue=2 | title=Stromelysin-3 expression in the differential diagnosis of dermatofibroma and dermatofibrosarcoma protuberans: comparison with factor XIIIa and CD34 | year=2007 | month=August | author=Kim HJ, Lee JY, Kim SH, &#039;&#039;et al.&#039;&#039; | journal=Br. J. Dermatol. | pages=319–24}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
!  [[Factor XIIIa]]&amp;lt;ref&amp;gt;http://emedicine.medscape.com/article/1056742-overview&amp;lt;/ref&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|  Dermatofibroma&lt;br /&gt;
|  +&lt;br /&gt;
|  +&lt;br /&gt;
|  +&lt;br /&gt;
|-&lt;br /&gt;
|  [[Dermatofibrosarcoma protuberans]]&lt;br /&gt;
|  +&lt;br /&gt;
|  -&lt;br /&gt;
|  - &lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&lt;br /&gt;
{{Reflist|2}}&lt;br /&gt;
[[Category:Needs overview]]&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Dermatology]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Oncology]]&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Dermatofibroma_pathophysiology&amp;diff=865949</id>
		<title>Dermatofibroma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Dermatofibroma_pathophysiology&amp;diff=865949"/>
		<updated>2013-04-01T14:44:38Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Dermatofibroma}}&lt;br /&gt;
{{CMG}}&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
* Some physicians and researchers believe dermatofibromas form as a reaction to previous injuries such as insect bites or thorn pricks.&lt;br /&gt;
* Dermatofibromas are composed of disordered [[collagen]] laid down by [[fibroblasts]].&lt;br /&gt;
&lt;br /&gt;
===Immunohistochemical staining===&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
!  Neoplasm&lt;br /&gt;
!  [[CD34]]&lt;br /&gt;
!  [[Stromelysin-3]]&amp;lt;ref&amp;gt;{{cite journal | pmid = 17596171 | doi=10.1111/j.1365-2133.2007.08033.x | volume=157 | issue=2 | title=Stromelysin-3 expression in the differential diagnosis of dermatofibroma and dermatofibrosarcoma protuberans: comparison with factor XIIIa and CD34 | year=2007 | month=August | author=Kim HJ, Lee JY, Kim SH, &#039;&#039;et al.&#039;&#039; | journal=Br. J. Dermatol. | pages=319–24}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
!  [[Factor XIIIa]]&amp;lt;ref&amp;gt;http://emedicine.medscape.com/article/1056742-overview&amp;lt;/ref&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|  Dermatofibroma&lt;br /&gt;
|  +&lt;br /&gt;
|  +&lt;br /&gt;
|  +&lt;br /&gt;
|-&lt;br /&gt;
|  [[Dermatofibrosarcoma protuberans]]&lt;br /&gt;
|  +&lt;br /&gt;
|  -&lt;br /&gt;
|  - &lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&lt;br /&gt;
{{Reflist|2}}&lt;br /&gt;
[[Category:Needs overview]]&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Dermatology]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Oncology]]&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Dermatofibroma_pathophysiology&amp;diff=865948</id>
		<title>Dermatofibroma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Dermatofibroma_pathophysiology&amp;diff=865948"/>
		<updated>2013-04-01T14:44:14Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Dermatofibroma}}&lt;br /&gt;
{{CMG}}&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
* Some physicians and researchers believe dermatofibromas form as a reaction to previous injuries such as insect bites or thorn pricks.&lt;br /&gt;
* Dermatofibromas are composed of disordered [[collagen]] laid down by [[fibroblasts]].&lt;br /&gt;
&lt;br /&gt;
===Immunohistochemical staining===&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
!  Neoplasm&lt;br /&gt;
!  [[CD34]]&amp;lt;ref name=&amp;quot;Bolognia&amp;quot; /&amp;gt;&lt;br /&gt;
!  [[Stromelysin-3]]&amp;lt;ref&amp;gt;{{cite journal | pmid = 17596171 | doi=10.1111/j.1365-2133.2007.08033.x | volume=157 | issue=2 | title=Stromelysin-3 expression in the differential diagnosis of dermatofibroma and dermatofibrosarcoma protuberans: comparison with factor XIIIa and CD34 | year=2007 | month=August | author=Kim HJ, Lee JY, Kim SH, &#039;&#039;et al.&#039;&#039; | journal=Br. J. Dermatol. | pages=319–24}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
!  [[Factor XIIIa]]&amp;lt;ref&amp;gt;http://emedicine.medscape.com/article/1056742-overview&amp;lt;/ref&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|  Dermatofibroma&lt;br /&gt;
|  +&lt;br /&gt;
|  +&lt;br /&gt;
|  +&lt;br /&gt;
|-&lt;br /&gt;
|  [[Dermatofibrosarcoma protuberans]]&lt;br /&gt;
|  +&lt;br /&gt;
|  -&lt;br /&gt;
|  - &lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&lt;br /&gt;
{{Reflist|2}}&lt;br /&gt;
[[Category:Needs overview]]&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Dermatology]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Oncology]]&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Dermatofibroma_pathophysiology&amp;diff=865947</id>
		<title>Dermatofibroma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Dermatofibroma_pathophysiology&amp;diff=865947"/>
		<updated>2013-04-01T14:39:45Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Dermatofibroma}}&lt;br /&gt;
{{CMG}}&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
* Some physicians and researchers believe dermatofibromas form as a reaction to previous injuries such as insect bites or thorn pricks.&lt;br /&gt;
* Dermatofibromas are composed of disordered [[collagen]] laid down by [[fibroblasts]].&lt;br /&gt;
&lt;br /&gt;
===Immunohistochemical staining===&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
!  Neoplasm&lt;br /&gt;
!  [[CD34]]&amp;lt;ref name=&amp;quot;Bolognia&amp;quot; /&amp;gt;&lt;br /&gt;
!  [[Stromelysin-3]]&amp;lt;ref&amp;gt;{{cite journal | pmid = 17596171 | doi=10.1111/j.1365-2133.2007.08033.x | volume=157 | issue=2 | title=Stromelysin-3 expression in the differential diagnosis of dermatofibroma and dermatofibrosarcoma protuberans: comparison with factor XIIIa and CD34 | year=2007 | month=August | author=Kim HJ, Lee JY, Kim SH, &#039;&#039;et al.&#039;&#039; | journal=Br. J. Dermatol. | pages=319–24}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
!  [[Factor XIIIa]]&amp;lt;ref&amp;gt;http://emedicine.medscape.com/article/1056742-overview&amp;lt;/ref&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|  Dermatofibroma&lt;br /&gt;
|  +&lt;br /&gt;
|  +&lt;br /&gt;
|  +&lt;br /&gt;
|-&lt;br /&gt;
|  [[Dermatofibrosarcoma protuberans]]&lt;br /&gt;
|  +&lt;br /&gt;
|  -&lt;br /&gt;
|  - &lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Category:Needs overview]]&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Dermatology]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Oncology]]&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=File:800px-Ovarian_clear_cell_carcinoma_-_very_high_mag.jpg&amp;diff=862651</id>
		<title>File:800px-Ovarian clear cell carcinoma - very high mag.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=File:800px-Ovarian_clear_cell_carcinoma_-_very_high_mag.jpg&amp;diff=862651"/>
		<updated>2013-03-19T15:18:54Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=File:734px-Choroid_plexus_papilloma_micrograph.jpg&amp;diff=862642</id>
		<title>File:734px-Choroid plexus papilloma micrograph.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=File:734px-Choroid_plexus_papilloma_micrograph.jpg&amp;diff=862642"/>
		<updated>2013-03-19T15:09:37Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=File:Plexuspapillom_Makroskopie.png&amp;diff=862641</id>
		<title>File:Plexuspapillom Makroskopie.png</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=File:Plexuspapillom_Makroskopie.png&amp;diff=862641"/>
		<updated>2013-03-19T15:06:39Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862306</id>
		<title>Gestational trophoblastic neoplasia pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862306"/>
		<updated>2013-03-18T13:53:50Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Choriocarcinoma}}&lt;br /&gt;
{{CMG}};{{AE}}{{SM}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
&lt;br /&gt;
===Microscopic Pathology===&lt;br /&gt;
On [[light microscopy]], there is malignant [[trophoblast]]ic proliferation without hydropic villi.Characteristic feature is the identification of intimately related [[syncytiotrophoblast]]s and [[cytotrophoblast]]s without formation of definite placental type villi.Syncytiotrophoblasts are large multi-nucleated cells with [[eosinophilic]] [[cytoplasm]].  They often surround the cytotrophoblasts, reminiscent of their normal anatomical relationship in [[chorionic villi]].  Cytotrophoblasts are polyhedral, mononuclear cells with hyperchromatic nuclei and a clear or pale cytoplasm.  Extensive [[hemorrhage]] is a common finding.Shown below is an image of choriocarcinoma.(High mag|H&amp;amp;E stain)&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Choriocarcinoma_-2-_very_high_mag.jpg‎|200px]]&lt;br /&gt;
&lt;br /&gt;
The Image shows:&lt;br /&gt;
&lt;br /&gt;
Choriocarcinomas consist of two cell populations:&lt;br /&gt;
#[[w:cytotrophoblast|Cytotrophoblasts]].&lt;br /&gt;
#*Pale/clear cytoplasm.&lt;br /&gt;
#[[w:Syncytiotrophoblast|Syncytiotrophoblasts]].&lt;br /&gt;
#*Hyperchromatic cytoplasm.&lt;br /&gt;
#*Typically multinucleated.&lt;br /&gt;
&lt;br /&gt;
Traditionally, the syncytiotrophoblasts are said to produce the beta-hCG;&amp;lt;ref name=pmid20735820&amp;gt;{{Cite journal  | last1 = Cole | first1 = LA. | title = Biological functions of hCG and hCG-related molecules. | journal = Reprod Biol Endocrinol | volume = 8 | issue =  | pages = 102 | month =  | year = 2010 | doi = 10.1186/1477-7827-8-102 | PMID = 20735820 | PMC = 2936313 | URL = http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936313/ }}&amp;lt;/ref&amp;gt;however, it has been determined that cytotrophoblast also produce some.&amp;lt;ref name=pmid12242037&amp;gt;{{Cite journal  | last1 = Kovalevskaya | first1 = G. | last2 = Genbacev | first2 = O. | last3 = Fisher | first3 = SJ. | last4 = Caceres | first4 = E. | last5 = O&#039;Connor | first5 = JF. | title = Trophoblast origin of hCG isoforms: cytotrophoblasts are the primary source of choriocarcinoma-like hCG. | journal = Mol Cell Endocrinol | volume = 194 | issue = 1-2 | pages = 147-55 | month = Aug | year = 2002 | doi =  | PMID = 12242037 }}&amp;lt;/ref&amp;gt;The syncytiotrophoblasts are often arranged around the outside of cytotrophoblast cell clusters, reminicent of the arrangement in the [[w:placenta|placenta]].  On placental [[w:Chorionic_villi|villi]], the syncytiotrophoblasts are superficial to and, early in [[w:pregnancy|pregnancy]], cover the cytotrophoblast.Choriocarcinoma is classified as a [[w:germ cell tumour|germ cell tumour]].  It can arise in the [[w:testis|testis]] or [[w:ovary|ovary]] and from a [[w:hydatidiform mole|hydatidiform mole]].  It may be part of a [[w:mixed germ cell tumour|mixed germ cell tumour]].&lt;br /&gt;
&lt;br /&gt;
===Video===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{#ev:youtube|X6PZ0nRM554}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Needs overview]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Gynecology]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
&lt;br /&gt;
{{WH}}&lt;br /&gt;
{{WS}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862305</id>
		<title>Gestational trophoblastic neoplasia pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862305"/>
		<updated>2013-03-18T13:53:33Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Choriocarcinoma}}&lt;br /&gt;
{{CMG}};{{AE}}{{SM}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
&lt;br /&gt;
===Microscopic Pathology===&lt;br /&gt;
On [[light microscopy]], there is malignant [[trophoblast]]ic proliferation without hydropic villi.Characteristic feature is the identification of intimately related [[syncytiotrophoblast]]s and [[cytotrophoblast]]s without formation of definite placental type villi.Syncytiotrophoblasts are large multi-nucleated cells with [[eosinophilic]] [[cytoplasm]].  They often surround the cytotrophoblasts, reminiscent of their normal anatomical relationship in [[chorionic villi]].  Cytotrophoblasts are polyhedral, mononuclear cells with hyperchromatic nuclei and a clear or pale cytoplasm.  Extensive [[hemorrhage]] is a common finding.Shown below is an image of choriocarcinoma.(High mag|H&amp;amp;E stain)&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Choriocarcinoma_-2-_very_high_mag.jpg‎|200px]]&lt;br /&gt;
&lt;br /&gt;
The Image shows:&lt;br /&gt;
&lt;br /&gt;
Choriocarcinomas consist of two cell populations:&lt;br /&gt;
#[[w:cytotrophoblast|Cytotrophoblasts]].&lt;br /&gt;
#*Pale/clear cytoplasm.&lt;br /&gt;
#[[w:Syncytiotrophoblast|Syncytiotrophoblasts]].&lt;br /&gt;
#*Hyperchromatic cytoplasm.&lt;br /&gt;
#*Typically multinucleated.&lt;br /&gt;
&lt;br /&gt;
Traditionally, the syncytiotrophoblasts are said to produce the beta-hCG;&amp;lt;ref name=pmid20735820&amp;gt;{{Cite journal  | last1 = Cole | first1 = LA. | title = Biological functions of hCG and hCG-related molecules. | journal = Reprod Biol Endocrinol | volume = 8 | issue =  | pages = 102 | month =  | year = 2010 | doi = 10.1186/1477-7827-8-102 | PMID = 20735820 | PMC = 2936313 | URL = http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936313/ }}&amp;lt;/ref&amp;gt;however, it has been determined that cytotrophoblast also produce some.&amp;lt;ref name=pmid12242037&amp;gt;{{Cite journal  | last1 = Kovalevskaya | first1 = G. | last2 = Genbacev | first2 = O. | last3 = Fisher | first3 = SJ. | last4 = Caceres | first4 = E. | last5 = O&#039;Connor | first5 = JF. | title = Trophoblast origin of hCG isoforms: cytotrophoblasts are the primary source of choriocarcinoma-like hCG. | journal = Mol Cell Endocrinol | volume = 194 | issue = 1-2 | pages = 147-55 | month = Aug | year = 2002 | doi =  | PMID = 12242037 }}&amp;lt;/ref&amp;gt;The syncytiotrophoblasts are often arranged around the outside of cytotrophoblast cell clusters, reminicent of the arrangement in the [[w:placenta|placenta]].  On placental [[w:Chorionic_villi|villi]], the syncytiotrophoblasts are superficial to and, early in [[w:pregnancy|pregnancy]], cover the cytotrophoblast.Choriocarcinoma is classified as a [[w:germ cell tumour|germ cell tumour]].  It can arise in the [[w:testis|testis]] or [[w:ovary|ovary]] and from a [[w:hydatidiform mole|hydatidiform mole]].  It may be part of a [[w:mixed germ cell tumour|mixed germ cell tumour]].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Video===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{#ev:youtube|X6PZ0nRM554}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Needs overview]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Gynecology]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
&lt;br /&gt;
{{WH}}&lt;br /&gt;
{{WS}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862303</id>
		<title>Gestational trophoblastic neoplasia pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862303"/>
		<updated>2013-03-18T13:52:56Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Choriocarcinoma}}&lt;br /&gt;
{{CMG}};{{AE}}{{SM}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
&lt;br /&gt;
===Microscopic Pathology===&lt;br /&gt;
On [[light microscopy]], there is malignant [[trophoblast]]ic proliferation without hydropic villi.Characteristic feature is the identification of intimately related [[syncytiotrophoblast]]s and [[cytotrophoblast]]s without formation of definite placental type villi.Syncytiotrophoblasts are large multi-nucleated cells with [[eosinophilic]] [[cytoplasm]].  They often surround the cytotrophoblasts, reminiscent of their normal anatomical relationship in [[chorionic villi]].  Cytotrophoblasts are polyhedral, mononuclear cells with hyperchromatic nuclei and a clear or pale cytoplasm.  Extensive [[hemorrhage]] is a common finding.Shown below is an image of choriocarcinoma.(High mag|H&amp;amp;E stain)&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Choriocarcinoma_-2-_very_high_mag.jpg‎|200px]]&lt;br /&gt;
&lt;br /&gt;
The Image shows:&lt;br /&gt;
&lt;br /&gt;
Choriocarcinomas consist of two cell populations:&lt;br /&gt;
#[[w:cytotrophoblast|Cytotrophoblasts]].&lt;br /&gt;
#*Pale/clear cytoplasm.&lt;br /&gt;
#[[w:Syncytiotrophoblast|Syncytiotrophoblasts]].&lt;br /&gt;
#*Hyperchromatic cytoplasm.&lt;br /&gt;
#*Typically multinucleated.&lt;br /&gt;
&lt;br /&gt;
Traditionally, the syncytiotrophoblasts are said to produce the beta-hCG;&amp;lt;ref name=pmid20735820&amp;gt;{{Cite journal  | last1 = Cole | first1 = LA. | title = Biological functions of hCG and hCG-related molecules. | journal = Reprod Biol Endocrinol | volume = 8 | issue =  | pages = 102 | month =  | year = 2010 | doi = 10.1186/1477-7827-8-102 | PMID = 20735820 | PMC = 2936313 | URL = http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936313/ }}&amp;lt;/ref&amp;gt;however, it has been determined that cytotrophoblast also produce some.&amp;lt;ref name=pmid12242037&amp;gt;{{Cite journal  | last1 = Kovalevskaya | first1 = G. | last2 = Genbacev | first2 = O. | last3 = Fisher | first3 = SJ. | last4 = Caceres | first4 = E. | last5 = O&#039;Connor | first5 = JF. | title = Trophoblast origin of hCG isoforms: cytotrophoblasts are the primary source of choriocarcinoma-like hCG. | journal = Mol Cell Endocrinol | volume = 194 | issue = 1-2 | pages = 147-55 | month = Aug | year = 2002 | doi =  | PMID = 12242037 }}&amp;lt;/ref&amp;gt;The syncytiotrophoblasts are often arranged around the outside of cytotrophoblast cell clusters, reminicent of the arrangement in the [[w:placenta|placenta]].  On placental [[w:Chorionic_villi|villi]], the syncytiotrophoblasts are superficial to and, early in [[w:pregnancy|pregnancy]], cover the cytotrophoblast.Choriocarcinoma is classified as a [[w:germ cell tumour|germ cell tumour]].  It can arise in the [[w:testis|testis]] or [[w:ovary|ovary]] and from a [[w:hydatidiform mole|hydatidiform mole]].  It may be part of a [[w:mixed germ cell tumour|mixed germ cell tumour]].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Video===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{#ev:youtube|X6PZ0nRM554}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Gynecology]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
&lt;br /&gt;
{{WH}}&lt;br /&gt;
{{WS}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862302</id>
		<title>Gestational trophoblastic neoplasia pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862302"/>
		<updated>2013-03-18T13:52:29Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Choriocarcinoma}}&lt;br /&gt;
{{CMG}};{{AE}}{{SM}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
&lt;br /&gt;
===Microscopic Pathology===&lt;br /&gt;
On [[light microscopy]], there is malignant [[trophoblast]]ic proliferation without hydropic villi.Characteristic feature is the identification of intimately related [[syncytiotrophoblast]]s and [[cytotrophoblast]]s without formation of definite placental type villi.Syncytiotrophoblasts are large multi-nucleated cells with [[eosinophilic]] [[cytoplasm]].  They often surround the cytotrophoblasts, reminiscent of their normal anatomical relationship in [[chorionic villi]].  Cytotrophoblasts are polyhedral, mononuclear cells with hyperchromatic nuclei and a clear or pale cytoplasm.  Extensive [[hemorrhage]] is a common finding.Shown below is an image of choriocarcinoma.(High mag|H&amp;amp;E stain)&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Choriocarcinoma_-2-_very_high_mag.jpg‎|200px]]&lt;br /&gt;
&lt;br /&gt;
The Image shows:&lt;br /&gt;
&lt;br /&gt;
Choriocarcinomas consist of two cell populations:&lt;br /&gt;
#[[w:cytotrophoblast|Cytotrophoblasts]].&lt;br /&gt;
#*Pale/clear cytoplasm.&lt;br /&gt;
#[[w:Syncytiotrophoblast|Syncytiotrophoblasts]].&lt;br /&gt;
#*Hyperchromatic cytoplasm.&lt;br /&gt;
#*Typically multinucleated.&lt;br /&gt;
&lt;br /&gt;
Traditionally, the syncytiotrophoblasts are said to produce the beta-hCG;&amp;lt;ref name=pmid20735820&amp;gt;{{Cite journal  | last1 = Cole | first1 = LA. | title = Biological functions of hCG and hCG-related molecules. | journal = Reprod Biol Endocrinol | volume = 8 | issue =  | pages = 102 | month =  | year = 2010 | doi = 10.1186/1477-7827-8-102 | PMID = 20735820 | PMC = 2936313 | URL = http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936313/ }}&amp;lt;/ref&amp;gt;however, it has been determined that cytotrophoblast also produce some.&amp;lt;ref name=pmid12242037&amp;gt;{{Cite journal  | last1 = Kovalevskaya | first1 = G. | last2 = Genbacev | first2 = O. | last3 = Fisher | first3 = SJ. | last4 = Caceres | first4 = E. | last5 = O&#039;Connor | first5 = JF. | title = Trophoblast origin of hCG isoforms: cytotrophoblasts are the primary source of choriocarcinoma-like hCG. | journal = Mol Cell Endocrinol | volume = 194 | issue = 1-2 | pages = 147-55 | month = Aug | year = 2002 | doi =  | PMID = 12242037 }}&amp;lt;/ref&amp;gt;The syncytiotrophoblasts are often arranged around the outside of cytotrophoblast cell clusters, reminicent of the arrangement in the [[w:placenta|placenta]].  On placental [[w:Chorionic_villi|villi]], the syncytiotrophoblasts are superficial to and, early in [[w:pregnancy|pregnancy]], cover the cytotrophoblast.Choriocarcinoma is classified as a [[w:germ cell tumour|germ cell tumour]].  It can arise in the [[w:testis|testis]] or [[w:ovary|ovary]] and from a [[w:hydatidiform mole|hydatidiform mole]].  It may be part of a [[w:mixed germ cell tumour|mixed germ cell tumour]].&lt;br /&gt;
&lt;br /&gt;
===Video===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{#ev:youtube|X6PZ0nRM554}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Gynecology]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
&lt;br /&gt;
{{WH}}&lt;br /&gt;
{{WS}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862299</id>
		<title>Gestational trophoblastic neoplasia pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862299"/>
		<updated>2013-03-18T13:51:40Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Choriocarcinoma}}&lt;br /&gt;
{{CMG}};{{AE}}{{SM}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
&lt;br /&gt;
===Microscopic Pathology===&lt;br /&gt;
On [[light microscopy]], there is malignant [[trophoblast]]ic proliferation without hydropic villi.Characteristic feature is the identification of intimately related [[syncytiotrophoblast]]s and [[cytotrophoblast]]s without formation of definite placental type villi.Syncytiotrophoblasts are large multi-nucleated cells with [[eosinophilic]] [[cytoplasm]].  They often surround the cytotrophoblasts, reminiscent of their normal anatomical relationship in [[chorionic villi]].  Cytotrophoblasts are polyhedral, mononuclear cells with hyperchromatic nuclei and a clear or pale cytoplasm.  Extensive [[hemorrhage]] is a common finding.Shown below is an image of choriocarcinoma.(High mag|H&amp;amp;E stain)&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Choriocarcinoma_-2-_very_high_mag.jpg‎|200px]]&lt;br /&gt;
&lt;br /&gt;
The Image shows:&lt;br /&gt;
&lt;br /&gt;
Choriocarcinomas consist of two cell populations:&lt;br /&gt;
#[[w:cytotrophoblast|Cytotrophoblasts]].&lt;br /&gt;
#*Pale/clear cytoplasm.&lt;br /&gt;
#[[w:Syncytiotrophoblast|Syncytiotrophoblasts]].&lt;br /&gt;
#*Hyperchromatic cytoplasm.&lt;br /&gt;
#*Typically multinucleated.&lt;br /&gt;
&lt;br /&gt;
===Video===&lt;br /&gt;
&lt;br /&gt;
{{#ev:youtube|X6PZ0nRM554}}&lt;br /&gt;
Traditionally, the syncytiotrophoblasts are said to produce the beta-hCG;&amp;lt;ref name=pmid20735820&amp;gt;{{Cite journal  | last1 = Cole | first1 = LA. | title = Biological functions of hCG and hCG-related molecules. | journal = Reprod Biol Endocrinol | volume = 8 | issue =  | pages = 102 | month =  | year = 2010 | doi = 10.1186/1477-7827-8-102 | PMID = 20735820 | PMC = 2936313 | URL = http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936313/ }}&amp;lt;/ref&amp;gt;however, it has been determined that cytotrophoblast also produce some.&amp;lt;ref name=pmid12242037&amp;gt;{{Cite journal  | last1 = Kovalevskaya | first1 = G. | last2 = Genbacev | first2 = O. | last3 = Fisher | first3 = SJ. | last4 = Caceres | first4 = E. | last5 = O&#039;Connor | first5 = JF. | title = Trophoblast origin of hCG isoforms: cytotrophoblasts are the primary source of choriocarcinoma-like hCG. | journal = Mol Cell Endocrinol | volume = 194 | issue = 1-2 | pages = 147-55 | month = Aug | year = 2002 | doi =  | PMID = 12242037 }}&amp;lt;/ref&amp;gt;The syncytiotrophoblasts are often arranged around the outside of cytotrophoblast cell clusters, reminicent of the arrangement in the [[w:placenta|placenta]].  On placental [[w:Chorionic_villi|villi]], the syncytiotrophoblasts are superficial to and, early in [[w:pregnancy|pregnancy]], cover the cytotrophoblast.Choriocarcinoma is classified as a [[w:germ cell tumour|germ cell tumour]].  It can arise in the [[w:testis|testis]] or [[w:ovary|ovary]] and from a [[w:hydatidiform mole|hydatidiform mole]].  It may be part of a [[w:mixed germ cell tumour|mixed germ cell tumour]].&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Gynecology]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
&lt;br /&gt;
{{WH}}&lt;br /&gt;
{{WS}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862294</id>
		<title>Gestational trophoblastic neoplasia pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862294"/>
		<updated>2013-03-18T13:47:16Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: /* Microscopic Pathology */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Choriocarcinoma}}&lt;br /&gt;
{{CMG}};{{AE}}{{SM}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
&lt;br /&gt;
===Microscopic Pathology===&lt;br /&gt;
On [[light microscopy]], there is malignant [[trophoblast]]ic proliferation without hydropic villi.Characteristic feature is the identification of intimately related [[syncytiotrophoblast]]s and [[cytotrophoblast]]s without formation of definite placental type villi.Syncytiotrophoblasts are large multi-nucleated cells with [[eosinophilic]] [[cytoplasm]].  They often surround the cytotrophoblasts, reminiscent of their normal anatomical relationship in [[chorionic villi]].  Cytotrophoblasts are polyhedral, mononuclear cells with hyperchromatic nuclei and a clear or pale cytoplasm.  Extensive [[hemorrhage]] is a common finding.Shown below is an image of choriocarcinoma.(High mag|H&amp;amp;E stain)&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Choriocarcinoma_-2-_very_high_mag.jpg‎|200px]]&lt;br /&gt;
&lt;br /&gt;
The Image shows:&lt;br /&gt;
&lt;br /&gt;
Choriocarcinomas consist of two cell populations:&lt;br /&gt;
#[[w:cytotrophoblast|Cytotrophoblasts]].&lt;br /&gt;
#*Pale/clear cytoplasm.&lt;br /&gt;
#[[w:Syncytiotrophoblast|Syncytiotrophoblasts]].&lt;br /&gt;
#*Hyperchromatic cytoplasm.&lt;br /&gt;
#*Typically multinucleated.&lt;br /&gt;
&lt;br /&gt;
Traditionally, the syncytiotrophoblasts are said to produce the beta-hCG;&amp;lt;ref name=pmid20735820&amp;gt;{{Cite journal  | last1 = Cole | first1 = LA. | title = Biological functions of hCG and hCG-related molecules. | journal = Reprod Biol Endocrinol | volume = 8 | issue =  | pages = 102 | month =  | year = 2010 | doi = 10.1186/1477-7827-8-102 | PMID = 20735820 | PMC = 2936313 | URL = http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936313/ }}&amp;lt;/ref&amp;gt;however, it has been determined that cytotrophoblast also produce some.&amp;lt;ref name=pmid12242037&amp;gt;{{Cite journal  | last1 = Kovalevskaya | first1 = G. | last2 = Genbacev | first2 = O. | last3 = Fisher | first3 = SJ. | last4 = Caceres | first4 = E. | last5 = O&#039;Connor | first5 = JF. | title = Trophoblast origin of hCG isoforms: cytotrophoblasts are the primary source of choriocarcinoma-like hCG. | journal = Mol Cell Endocrinol | volume = 194 | issue = 1-2 | pages = 147-55 | month = Aug | year = 2002 | doi =  | PMID = 12242037 }}&amp;lt;/ref&amp;gt;The syncytiotrophoblasts are often arranged around the outside of cytotrophoblast cell clusters, reminicent of the arrangement in the [[w:placenta|placenta]].  On placental [[w:Chorionic_villi|villi]], the syncytiotrophoblasts are superficial to and, early in [[w:pregnancy|pregnancy]], cover the cytotrophoblast.Choriocarcinoma is classified as a [[w:germ cell tumour|germ cell tumour]].  It can arise in the [[w:testis|testis]] or [[w:ovary|ovary]] and from a [[w:hydatidiform mole|hydatidiform mole]].  It may be part of a [[w:mixed germ cell tumour|mixed germ cell tumour]].&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Gynecology]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
&lt;br /&gt;
{{WH}}&lt;br /&gt;
{{WS}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862293</id>
		<title>Gestational trophoblastic neoplasia pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862293"/>
		<updated>2013-03-18T13:46:16Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Choriocarcinoma}}&lt;br /&gt;
{{CMG}};{{AE}}{{SM}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
&lt;br /&gt;
===Microscopic Pathology===&lt;br /&gt;
On [[light microscopy]], there is malignant [[trophoblast]]ic proliferation without hydropic villi.Characteristic feature is the identification of intimately related [[syncytiotrophoblast]]s and [[cytotrophoblast]]s without formation of definite placental type villi.Syncytiotrophoblasts are large multi-nucleated cells with [[eosinophilic]] [[cytoplasm]].  They often surround the cytotrophoblasts, reminiscent of their normal anatomical relationship in [[chorionic villi]].  Cytotrophoblasts are polyhedral, mononuclear cells with hyperchromatic nuclei and a clear or pale cytoplasm.  Extensive [[hemorrhage]] is a common finding.Shown below is an image of choriocarcinoma.&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Choriocarcinoma_-2-_very_high_mag.jpg‎|200px]]&lt;br /&gt;
&lt;br /&gt;
The Image shows:&lt;br /&gt;
&lt;br /&gt;
Choriocarcinomas consist of two cell populations:&lt;br /&gt;
#[[w:cytotrophoblast|Cytotrophoblasts]].&lt;br /&gt;
#*Pale/clear cytoplasm.&lt;br /&gt;
#[[w:Syncytiotrophoblast|Syncytiotrophoblasts]].&lt;br /&gt;
#*Hyperchromatic cytoplasm.&lt;br /&gt;
#*Typically multinucleated.&lt;br /&gt;
&lt;br /&gt;
Traditionally, the syncytiotrophoblasts are said to produce the beta-hCG;&amp;lt;ref name=pmid20735820&amp;gt;{{Cite journal  | last1 = Cole | first1 = LA. | title = Biological functions of hCG and hCG-related molecules. | journal = Reprod Biol Endocrinol | volume = 8 | issue =  | pages = 102 | month =  | year = 2010 | doi = 10.1186/1477-7827-8-102 | PMID = 20735820 | PMC = 2936313 | URL = http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936313/ }}&amp;lt;/ref&amp;gt;however, it has been determined that cytotrophoblast also produce some.&amp;lt;ref name=pmid12242037&amp;gt;{{Cite journal  | last1 = Kovalevskaya | first1 = G. | last2 = Genbacev | first2 = O. | last3 = Fisher | first3 = SJ. | last4 = Caceres | first4 = E. | last5 = O&#039;Connor | first5 = JF. | title = Trophoblast origin of hCG isoforms: cytotrophoblasts are the primary source of choriocarcinoma-like hCG. | journal = Mol Cell Endocrinol | volume = 194 | issue = 1-2 | pages = 147-55 | month = Aug | year = 2002 | doi =  | PMID = 12242037 }}&amp;lt;/ref&amp;gt;The syncytiotrophoblasts are often arranged around the outside of cytotrophoblast cell clusters, reminicent of the arrangement in the [[w:placenta|placenta]].  On placental [[w:Chorionic_villi|villi]], the syncytiotrophoblasts are superficial to and, early in [[w:pregnancy|pregnancy]], cover the cytotrophoblast.Choriocarcinoma is classified as a [[w:germ cell tumour|germ cell tumour]].  It can arise in the [[w:testis|testis]] or [[w:ovary|ovary]] and from a [[w:hydatidiform mole|hydatidiform mole]].  It may be part of a [[w:mixed germ cell tumour|mixed germ cell tumour]].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Gynecology]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
&lt;br /&gt;
{{WH}}&lt;br /&gt;
{{WS}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862292</id>
		<title>Gestational trophoblastic neoplasia pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862292"/>
		<updated>2013-03-18T13:44:49Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Choriocarcinoma}}&lt;br /&gt;
{{CMG}};{{AE}}{{SM}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
&lt;br /&gt;
===Microscopic Pathology===&lt;br /&gt;
On [[light microscopy]], there is malignant [[trophoblast]]ic proliferation without hydropic villi.Characteristic feature is the identification of intimately related [[syncytiotrophoblast]]s and [[cytotrophoblast]]s without formation of definite placental type villi.&lt;br /&gt;
&lt;br /&gt;
Syncytiotrophoblasts are large multi-nucleated cells with [[eosinophilic]] [[cytoplasm]].  They often surround the cytotrophoblasts, reminiscent of their normal anatomical relationship in [[chorionic villi]].  Cytotrophoblasts are polyhedral, mononuclear cells with hyperchromatic nuclei and a clear or pale cytoplasm.  Extensive [[hemorrhage]] is a common finding.Shown below is an image of choriocarcinoma.&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Choriocarcinoma_-2-_very_high_mag.jpg‎|200px]]&lt;br /&gt;
&lt;br /&gt;
The Image shows:&lt;br /&gt;
Choriocarcinomas consist of two cell populations:&lt;br /&gt;
#[[w:cytotrophoblast|Cytotrophoblasts]].&lt;br /&gt;
#*Pale/clear cytoplasm.&lt;br /&gt;
#[[w:Syncytiotrophoblast|Syncytiotrophoblasts]].&lt;br /&gt;
#*Hyperchromatic cytoplasm.&lt;br /&gt;
#*Typically multinucleated.&lt;br /&gt;
&lt;br /&gt;
Traditionally, the syncytiotrophoblasts are said to produce the beta-hCG;&amp;lt;ref name=pmid20735820&amp;gt;{{Cite journal  | last1 = Cole | first1 = LA. | title = Biological functions of hCG and hCG-related molecules. | journal = Reprod Biol Endocrinol | volume = 8 | issue =  | pages = 102 | month =  | year = 2010 | doi = 10.1186/1477-7827-8-102 | PMID = 20735820 | PMC = 2936313 | URL = http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936313/ }}&amp;lt;/ref&amp;gt;however, it has been determined that cytotrophoblast also produce some.&amp;lt;ref name=pmid12242037&amp;gt;{{Cite journal  | last1 = Kovalevskaya | first1 = G. | last2 = Genbacev | first2 = O. | last3 = Fisher | first3 = SJ. | last4 = Caceres | first4 = E. | last5 = O&#039;Connor | first5 = JF. | title = Trophoblast origin of hCG isoforms: cytotrophoblasts are the primary source of choriocarcinoma-like hCG. | journal = Mol Cell Endocrinol | volume = 194 | issue = 1-2 | pages = 147-55 | month = Aug | year = 2002 | doi =  | PMID = 12242037 }}&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
The syncytiotrophoblasts are often arranged around the outside of cytotrophoblast cell clusters, reminicent of the arrangement in the [[w:placenta|placenta]].  On placental [[w:Chorionic_villi|villi]], the syncytiotrophoblasts are superficial to and, early in [[w:pregnancy|pregnancy]], cover the cytotrophoblast.&lt;br /&gt;
&lt;br /&gt;
Choriocarcinoma is classified as a [[w:germ cell tumour|germ cell tumour]].  It can arise in the [[w:testis|testis]] or [[w:ovary|ovary]] and from a [[w:hydatidiform mole|hydatidiform mole]].  It may be part of a [[w:mixed germ cell tumour|mixed germ cell tumour]].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Gynecology]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
&lt;br /&gt;
{{WH}}&lt;br /&gt;
{{WS}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862291</id>
		<title>Gestational trophoblastic neoplasia pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862291"/>
		<updated>2013-03-18T13:42:56Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Choriocarcinoma}}&lt;br /&gt;
{{CMG}};{{AE}}{{SM}}&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
&lt;br /&gt;
===Microscopic Pathology===&lt;br /&gt;
On [[light microscopy]], there is malignant [[trophoblast]]ic proliferation without hydropic villi.Characteristic feature is the identification of intimately related [[syncytiotrophoblast]]s and [[cytotrophoblast]]s without formation of definite placental type villi.&lt;br /&gt;
&lt;br /&gt;
Syncytiotrophoblasts are large multi-nucleated cells with [[eosinophilic]] [[cytoplasm]].  They often surround the cytotrophoblasts, reminiscent of their normal anatomical relationship in [[chorionic villi]].  Cytotrophoblasts are polyhedral, mononuclear cells with hyperchromatic nuclei and a clear or pale cytoplasm.  Extensive [[hemorrhage]] is a common finding.&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Choriocarcinoma_-2-_very_high_mag.jpg‎|200px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Gynecology]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
&lt;br /&gt;
{{WH}}&lt;br /&gt;
{{WS}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=File:800px-Choriocarcinoma_-2-_very_high_mag.jpg&amp;diff=862289</id>
		<title>File:800px-Choriocarcinoma -2- very high mag.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=File:800px-Choriocarcinoma_-2-_very_high_mag.jpg&amp;diff=862289"/>
		<updated>2013-03-18T13:41:37Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862286</id>
		<title>Gestational trophoblastic neoplasia pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Gestational_trophoblastic_neoplasia_pathophysiology&amp;diff=862286"/>
		<updated>2013-03-18T13:40:37Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Choriocarcinoma}}&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
&lt;br /&gt;
===Microscopic Pathology===&lt;br /&gt;
On [[light microscopy]], there is malignant [[trophoblast]]ic proliferation without hydropic villi.Characteristic feature is the identification of intimately related [[syncytiotrophoblast]]s and [[cytotrophoblast]]s without formation of definite placental type villi.&lt;br /&gt;
&lt;br /&gt;
Syncytiotrophoblasts are large multi-nucleated cells with [[eosinophilic]] [[cytoplasm]].  They often surround the cytotrophoblasts, reminiscent of their normal anatomical relationship in [[chorionic villi]].  Cytotrophoblasts are polyhedral, mononuclear cells with hyperchromatic nuclei and a clear or pale cytoplasm.  Extensive [[hemorrhage]] is a common finding.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Gynecology]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
&lt;br /&gt;
{{WH}}&lt;br /&gt;
{{WS}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Craniopharyngioma_pathophysiology&amp;diff=861597</id>
		<title>Craniopharyngioma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Craniopharyngioma_pathophysiology&amp;diff=861597"/>
		<updated>2013-03-13T18:11:54Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Craniopharyngioma}}&lt;br /&gt;
{{CMG}}&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
They are very slow growing tumors. They arise from the cells along the [[pituitary stalk]]. They are classified as [[benign]].&amp;lt;ref name=&amp;quot;pmid17630614&amp;quot;&amp;gt;{{cite journal |author=Garrè ML, Cama A |title=Craniopharyngioma: modern concepts in pathogenesis and treatment |journal=Curr. Opin. Pediatr. |volume=19 |issue=4 |pages=471-9 |year=2007 |pmid=17630614 |doi=10.1097/MOP.0b013e3282495a22}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Craniopharyngioma is a rare, usually [[suprasellar]]&amp;lt;ref name=&amp;quot;pmid17592268&amp;quot;&amp;gt;{{cite journal |author=Rodriguez FJ, Scheithauer BW, Tsunoda S, Kovacs K, Vidal S, Piepgras DG |title=The spectrum of malignancy in craniopharyngioma |journal=Am. J. Surg. Pathol. |volume=31 |issue=7 |pages=1020-8 |year=2007 |pmid=17592268 |doi=10.1097/PAS.0b013e31802d8a96}}&amp;lt;/ref&amp;gt; neoplasm, which may be [[cystic]], that develops from the nests of epithelium derived from [[Rathke&#039;s pouch]].&lt;br /&gt;
===Gross Pathology===&lt;br /&gt;
On macroscopic examination, craniopharyngiomas are cystic or partially cystic with solid areas.&lt;br /&gt;
&lt;br /&gt;
====Microscopic pathology====&lt;br /&gt;
The [[histologic]] pattern consists of nesting of [[squamous]] [[epithelium]] bordered by radially arranged cells. It is frequently accompanied by calcium deposition and have a microscopic papillary architecture.&lt;br /&gt;
Two distinct types are recognized:&amp;lt;ref name=&amp;quot;pmid12466115&amp;quot;&amp;gt;{{cite journal |author=Sekine S, Shibata T, Kokubu A, &#039;&#039;et al&#039;&#039; |title=Craniopharyngiomas of adamantinomatous type harbor beta-catenin gene mutations |journal=Am. J. Pathol. |volume=161 |issue=6 |pages=1997–2001 |year=2002 |month=December |pmid=12466115 |pmc=1850925 |doi= |url=http://ajp.amjpathol.org/cgi/pmidlookup?view=long&amp;amp;pmid=12466115}}&amp;lt;/ref&amp;gt;&amp;lt;ref name=&amp;quot;pmid15569047&amp;quot;&amp;gt;{{cite journal |author=Sekine S, Takata T, Shibata T, &#039;&#039;et al&#039;&#039; |title=Expression of enamel proteins and LEF1 in adamantinomatous craniopharyngioma: evidence for its odontogenic epithelial differentiation |journal=Histopathology |volume=45 |issue=6 |pages=573–9 |year=2004 |month=December |pmid=15569047 |doi=10.1111/j.1365-2559.2004.02029.x |url=http://www3.interscience.wiley.com/resolve/openurl?genre=article&amp;amp;sid=nlm:pubmed&amp;amp;issn=0309-0167&amp;amp;date=2004&amp;amp;volume=45&amp;amp;issue=6&amp;amp;spage=573}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
*Adamantinomatous craniopharyngioma and,&lt;br /&gt;
*Papillary craniopharyngioma.&lt;br /&gt;
&lt;br /&gt;
In the adamantinomatous type, calcifications are visible on neuroimaging and are helpful in diagnosis.&lt;br /&gt;
The papillary type rarely calcifies.&lt;br /&gt;
On light microscopy, the cysts are seen to be lined by stratified squamous epithelium. Keratin pearls may also be seen. The cysts are usually filled with a yellow, viscous fluid which is rich in cholesterol crystals. In addition to a long list of possible symptoms, the most common presentation include: headaches, growth failure, and [[bitemporal hemianopsia]].&lt;br /&gt;
&lt;br /&gt;
Shown below is a micrograph showing the characteristic features of an adamantinomatous craniopharyngioma - cystic spaces, calcifications, and &amp;quot;wet&amp;quot; keratin. HPS stain.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Adamantinomatous_craniopharyngioma_-_intermed_mag.jpg‎|200px]]&lt;br /&gt;
&lt;br /&gt;
Shown below is a Micrograph showing a papillary craniopharyngioma. HPS stain.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Papillary_craniopharyngioma_-_high_mag.jpg‎|200px]]&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{Reflist|2}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Needs overview]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Neurology]]&lt;br /&gt;
[[Category:Neurosurgery]]&lt;br /&gt;
&lt;br /&gt;
{{WikiDoc Help Menu}}&lt;br /&gt;
{{WikiDoc Sources}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Craniopharyngioma_pathophysiology&amp;diff=861596</id>
		<title>Craniopharyngioma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Craniopharyngioma_pathophysiology&amp;diff=861596"/>
		<updated>2013-03-13T18:10:18Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Craniopharyngioma}}&lt;br /&gt;
{{CMG}}&lt;br /&gt;
==Overview==&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
They are very slow growing tumors. They arise from the cells along the [[pituitary stalk]]. They are classified as [[benign]].&amp;lt;ref name=&amp;quot;pmid17630614&amp;quot;&amp;gt;{{cite journal |author=Garrè ML, Cama A |title=Craniopharyngioma: modern concepts in pathogenesis and treatment |journal=Curr. Opin. Pediatr. |volume=19 |issue=4 |pages=471-9 |year=2007 |pmid=17630614 |doi=10.1097/MOP.0b013e3282495a22}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Craniopharyngioma is a rare, usually [[suprasellar]]&amp;lt;ref name=&amp;quot;pmid17592268&amp;quot;&amp;gt;{{cite journal |author=Rodriguez FJ, Scheithauer BW, Tsunoda S, Kovacs K, Vidal S, Piepgras DG |title=The spectrum of malignancy in craniopharyngioma |journal=Am. J. Surg. Pathol. |volume=31 |issue=7 |pages=1020-8 |year=2007 |pmid=17592268 |doi=10.1097/PAS.0b013e31802d8a96}}&amp;lt;/ref&amp;gt; neoplasm, which may be [[cystic]], that develops from the nests of epithelium derived from [[Rathke&#039;s pouch]].&lt;br /&gt;
===Gross Pathology===&lt;br /&gt;
On macroscopic examination, craniopharyngiomas are cystic or partially cystic with solid areas.&lt;br /&gt;
&lt;br /&gt;
====Microscopic pathology====&lt;br /&gt;
The [[histologic]] pattern consists of nesting of [[squamous]] [[epithelium]] bordered by radially arranged cells. It is frequently accompanied by calcium deposition and have a microscopic papillary architecture.&lt;br /&gt;
Two distinct types are recognized:&amp;lt;ref name=&amp;quot;pmid12466115&amp;quot;&amp;gt;{{cite journal |author=Sekine S, Shibata T, Kokubu A, &#039;&#039;et al&#039;&#039; |title=Craniopharyngiomas of adamantinomatous type harbor beta-catenin gene mutations |journal=Am. J. Pathol. |volume=161 |issue=6 |pages=1997–2001 |year=2002 |month=December |pmid=12466115 |pmc=1850925 |doi= |url=http://ajp.amjpathol.org/cgi/pmidlookup?view=long&amp;amp;pmid=12466115}}&amp;lt;/ref&amp;gt;&amp;lt;ref name=&amp;quot;pmid15569047&amp;quot;&amp;gt;{{cite journal |author=Sekine S, Takata T, Shibata T, &#039;&#039;et al&#039;&#039; |title=Expression of enamel proteins and LEF1 in adamantinomatous craniopharyngioma: evidence for its odontogenic epithelial differentiation |journal=Histopathology |volume=45 |issue=6 |pages=573–9 |year=2004 |month=December |pmid=15569047 |doi=10.1111/j.1365-2559.2004.02029.x |url=http://www3.interscience.wiley.com/resolve/openurl?genre=article&amp;amp;sid=nlm:pubmed&amp;amp;issn=0309-0167&amp;amp;date=2004&amp;amp;volume=45&amp;amp;issue=6&amp;amp;spage=573}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
*Adamantinomatous craniopharyngioma and,&lt;br /&gt;
*Papillary craniopharyngioma.&lt;br /&gt;
&lt;br /&gt;
In the adamantinomatous type, calcifications are visible on neuroimaging and are helpful in diagnosis.&lt;br /&gt;
The papillary type rarely calcifies.&lt;br /&gt;
On light microscopy, the cysts are seen to be lined by stratified squamous epithelium. Keratin pearls may also be seen. The cysts are usually filled with a yellow, viscous fluid which is rich in cholesterol crystals. In addition to a long list of possible symptoms, the most common presentation include: headaches, growth failure, and [[bitemporal hemianopsia]].&lt;br /&gt;
&lt;br /&gt;
Shown below is a micrograph showing the characteristic features of an adamantinomatous craniopharyngioma - cystic spaces, calcifications, and &amp;quot;wet&amp;quot; keratin. HPS stain.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Adamantinomatous_craniopharyngioma_-_intermed_mag.jpg‎|200px]]&lt;br /&gt;
&lt;br /&gt;
Shown below is a Micrograph showing a papillary craniopharyngioma. HPS stain.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Papillary_craniopharyngioma_-_high_mag.jpg‎|200px]]&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{Reflist|2}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Neurology]]&lt;br /&gt;
[[Category:Neurosurgery]]&lt;br /&gt;
&lt;br /&gt;
{{WikiDoc Help Menu}}&lt;br /&gt;
{{WikiDoc Sources}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Craniopharyngioma_pathophysiology&amp;diff=861595</id>
		<title>Craniopharyngioma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Craniopharyngioma_pathophysiology&amp;diff=861595"/>
		<updated>2013-03-13T18:06:51Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Craniopharyngioma}}&lt;br /&gt;
{{CMG}}&lt;br /&gt;
==Overview==&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
They are very slow growing tumors. They arise from the cells along the [[pituitary stalk]]. They are classified as [[benign]].&amp;lt;ref name=&amp;quot;pmid17630614&amp;quot;&amp;gt;{{cite journal |author=Garrè ML, Cama A |title=Craniopharyngioma: modern concepts in pathogenesis and treatment |journal=Curr. Opin. Pediatr. |volume=19 |issue=4 |pages=471-9 |year=2007 |pmid=17630614 |doi=10.1097/MOP.0b013e3282495a22}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Craniopharyngioma is a rare, usually [[suprasellar]]&amp;lt;ref name=&amp;quot;pmid17592268&amp;quot;&amp;gt;{{cite journal |author=Rodriguez FJ, Scheithauer BW, Tsunoda S, Kovacs K, Vidal S, Piepgras DG |title=The spectrum of malignancy in craniopharyngioma |journal=Am. J. Surg. Pathol. |volume=31 |issue=7 |pages=1020-8 |year=2007 |pmid=17592268 |doi=10.1097/PAS.0b013e31802d8a96}}&amp;lt;/ref&amp;gt; neoplasm, which may be [[cystic]], that develops from the nests of epithelium derived from [[Rathke&#039;s pouch]]. &lt;br /&gt;
&lt;br /&gt;
====Microscopic pathology====&lt;br /&gt;
The [[histologic]] pattern consists of nesting of [[squamous]] [[epithelium]] bordered by radially arranged cells. It is frequently accompanied by calcium deposition and have a microscopic papillary architecture. Shown below is a micrograph showing the characteristic features of an adamantinomatous craniopharyngioma - cystic spaces, calcifications, and &amp;quot;wet&amp;quot; keratin. HPS stain.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Adamantinomatous_craniopharyngioma_-_intermed_mag.jpg‎|200px]]&lt;br /&gt;
&lt;br /&gt;
Shown below is a Micrograph showing a papillary craniopharyngioma. HPS stain.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-Papillary_craniopharyngioma_-_high_mag.jpg‎|200px]]&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{Reflist|2}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
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[[Category:Oncology]]&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
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[[Category:Neurology]]&lt;br /&gt;
[[Category:Neurosurgery]]&lt;br /&gt;
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{{WikiDoc Sources}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=File:800px-Papillary_craniopharyngioma_-_high_mag.jpg&amp;diff=861594</id>
		<title>File:800px-Papillary craniopharyngioma - high mag.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=File:800px-Papillary_craniopharyngioma_-_high_mag.jpg&amp;diff=861594"/>
		<updated>2013-03-13T18:05:09Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
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		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=File:800px-Adamantinomatous_craniopharyngioma_-_intermed_mag.jpg&amp;diff=861590</id>
		<title>File:800px-Adamantinomatous craniopharyngioma - intermed mag.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=File:800px-Adamantinomatous_craniopharyngioma_-_intermed_mag.jpg&amp;diff=861590"/>
		<updated>2013-03-13T18:01:21Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
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		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Chondrosarcoma_pathophysiology&amp;diff=861473</id>
		<title>Chondrosarcoma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Chondrosarcoma_pathophysiology&amp;diff=861473"/>
		<updated>2013-03-13T15:24:58Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Chondrosarcoma}}&lt;br /&gt;
{{CMG}};{{AE}}{{SM}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
===Microscopic Pathology===&lt;br /&gt;
Shown below is a micrograph of chondrosarcoma.(H&amp;amp;E stain)&lt;br /&gt;
&lt;br /&gt;
[[Image:Chondrosarcoma_(1).jpg‎|200px]]&lt;br /&gt;
===Video===&lt;br /&gt;
Below is a video of Extraskeletal Myxoid chondrosarcoma&lt;br /&gt;
{{#ev:youtube|DxljkFd9xew}}&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
[[Category:Orthopedics]]&lt;br /&gt;
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[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Skeletal disorders]]&lt;br /&gt;
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{{WikiDoc Help Menu}}&lt;br /&gt;
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		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Chondrosarcoma_pathophysiology&amp;diff=861472</id>
		<title>Chondrosarcoma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Chondrosarcoma_pathophysiology&amp;diff=861472"/>
		<updated>2013-03-13T15:24:42Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Chondrosarcoma}}&lt;br /&gt;
{{CMG}};{{AE}}{{SM}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
===Microscopic Pathology===&lt;br /&gt;
Shown below is a micrograph of chondrosarcoma.(H&amp;amp;E stain)&lt;br /&gt;
[[Image:Chondrosarcoma_(1).jpg‎|200px]]&lt;br /&gt;
===Video===&lt;br /&gt;
Below is a video of Extraskeletal Myxoid chondrosarcoma&lt;br /&gt;
{{#ev:youtube|DxljkFd9xew}}&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
[[Category:Orthopedics]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Skeletal disorders]]&lt;br /&gt;
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{{WikiDoc Help Menu}}&lt;br /&gt;
{{WikiDoc Sources}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
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	<entry>
		<id>https://www.wikidoc.org/index.php?title=File:Chondrosarcoma_(1).jpg&amp;diff=861468</id>
		<title>File:Chondrosarcoma (1).jpg</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=File:Chondrosarcoma_(1).jpg&amp;diff=861468"/>
		<updated>2013-03-13T15:22:30Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
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&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Chondrosarcoma_classification&amp;diff=861465</id>
		<title>Chondrosarcoma classification</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Chondrosarcoma_classification&amp;diff=861465"/>
		<updated>2013-03-13T15:21:42Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Chondrosarcoma}}&lt;br /&gt;
{{CMG}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
==Classification==&lt;br /&gt;
===Classification and Grading===&lt;br /&gt;
Physicians grade chondrosarcoma using several criteria, but particularly on how abnormal the cancerous cells appear under the microscope, and the growth rate of the tumors themselves, both of which are directly linked to the propensity of the cancer to invade locally, and to spread widely to distant organs and sites in the body (called [[metastasis]]).&lt;br /&gt;
&lt;br /&gt;
Grade 1 chondrosarcoma grows relatively slowly, has cells whose [[histological]] appearance is quite similar to cells of normal cartilage, and have much less aggressive invasive and metastatic properties. Grades 2 and 3 are increasingly faster-growing cancers, with more varied and abnormal-looking cells, and are much more likely to infiltrate surrounding tissues, lymph nodes, and organs. Some, but not all, authorities and medical facilities assign a &amp;quot;Grade 4&amp;quot; to the most [[anaplastic]], undifferentiated cartilage-derived tumors.&lt;br /&gt;
&lt;br /&gt;
The most common sites for chondrosarcoma to grow are the pelvis and shoulder, along with the superior [[metaphysis|metaphysial]] and [[diaphysis|diaphysial]] regions of the arms and legs.&amp;lt;ref name=&amp;quot;urlChondrosarcoma : Cancerbackup&amp;quot;&amp;gt;{{cite web |url=http://www.cancerbacup.org.uk/Cancertype/Bone/Typesofbonecancer/Chondrosarcoma#3340 |title=Chondrosarcoma : Cancerbackup |format= |work= |accessdate=2009-02-14}}&amp;lt;/ref&amp;gt; However, chondrosarcoma may occur in any bone, and are sometimes found in the skull, particularly at its base.&lt;br /&gt;
&lt;br /&gt;
[[ICD-O]] codes provide a more precise classification of chondrosarcoma. These &amp;quot;subtypes&amp;quot; are derived from, and reflect, both (a) the topographical location of the tumor, (b) the histological characteristics of the cancerous cartilage cells, and (c) the makeup of the surrounding matrix material associated with the tumor:&lt;br /&gt;
&lt;br /&gt;
* 9220 = Chondrosarcoma NOS (&amp;quot;Not Otherwise Specified&amp;quot;)&lt;br /&gt;
* 9221 = [[Juxtacortical chondrosarcoma]]&lt;br /&gt;
* 9231 = [[Myxoid chondrosarcoma]]&lt;br /&gt;
* 9240 = [[Mesenchymal chondrosarcoma]]&lt;br /&gt;
* 9242 = [[Clear cell chondrosarcoma]]&lt;br /&gt;
* 9243 = [[Dedifferentiated chondrosarcoma]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
[[Category:Orthopedics]]&lt;br /&gt;
[[Category:Needs overview]]&lt;br /&gt;
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[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Skeletal disorders]]&lt;br /&gt;
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{{WikiDoc Sources}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Chondrosarcoma_pathophysiology&amp;diff=861459</id>
		<title>Chondrosarcoma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Chondrosarcoma_pathophysiology&amp;diff=861459"/>
		<updated>2013-03-13T15:18:56Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Chondrosarcoma}}&lt;br /&gt;
{{CMG}}&lt;br /&gt;
&lt;br /&gt;
Please help WikiDoc by adding more content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
===Video===&lt;br /&gt;
Below is a video of Extraskeletal Myxoid chondrosarcoma&lt;br /&gt;
{{#ev:youtube|DxljkFd9xew}}&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
[[Category:Orthopedics]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Skeletal disorders]]&lt;br /&gt;
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{{WikiDoc Help Menu}}&lt;br /&gt;
{{WikiDoc Sources}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Chondroma_pathophysiology&amp;diff=861384</id>
		<title>Chondroma pathophysiology</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Chondroma_pathophysiology&amp;diff=861384"/>
		<updated>2013-03-13T13:45:26Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
{{Chondroma}}&lt;br /&gt;
{{CMG}}&lt;br /&gt;
Please help WikiDoc by adding more  content here.  It&#039;s easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.&lt;br /&gt;
&lt;br /&gt;
==Pathophysiology==&lt;br /&gt;
&lt;br /&gt;
===Video===&lt;br /&gt;
{{#ev:youtube|FLqr7Ld5-qc}}&lt;br /&gt;
&lt;br /&gt;
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&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
[[Category:Orthopedics]]&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
&lt;br /&gt;
[[Category:needs overview]]&lt;br /&gt;
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[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Skeletal disorders]]&lt;br /&gt;
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{{WikiDoc Help Menu}}&lt;br /&gt;
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		<author><name>Shivali Marketkar</name></author>
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	<entry>
		<id>https://www.wikidoc.org/index.php?title=Chondroma_classification&amp;diff=861383</id>
		<title>Chondroma classification</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Chondroma_classification&amp;diff=861383"/>
		<updated>2013-03-13T13:42:37Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{Chondroma}}&lt;br /&gt;
{{CMG}};&#039;&#039;&#039;Assistant Editor-in-Chief:&#039;&#039;&#039; Somal Khan&lt;br /&gt;
&lt;br /&gt;
==Overview==&lt;br /&gt;
Chondromas are classified according to their location.&lt;br /&gt;
[[Endochondromas]] : Tumor grows within the bone and expands it.&lt;br /&gt;
[[Ecchondroma]] - grows outward from the bone and this is rare. [[Periosteal]] chondomas are on the surface of the bone and other chondromas form in soft tissues.&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
[[Category:Orthopedics]]&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Skeletal disorders]]&lt;br /&gt;
&lt;br /&gt;
{{WikiDoc Help Menu}}&lt;br /&gt;
{{WikiDoc Sources}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Chondroma_classification&amp;diff=861382</id>
		<title>Chondroma classification</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Chondroma_classification&amp;diff=861382"/>
		<updated>2013-03-13T13:42:26Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{Chondroma}}&lt;br /&gt;
{{CMG}};&#039;&#039;&#039;Assistant Editor-in-Chief:&#039;&#039;&#039; Somal Khan&lt;br /&gt;
&lt;br /&gt;
==Overview==&lt;br /&gt;
Chondromas are classified according to their location.&lt;br /&gt;
[[Endochondromas]] : Tumor grows within the bone and expands it.&lt;br /&gt;
[[Ecchondroma]] - grows outward from the bone and this is rare. [[Periosteal]] chondomas are on the surface of the bone and other chondromas form in soft tissues.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
[[Category:Orthopedics]]&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Skeletal disorders]]&lt;br /&gt;
&lt;br /&gt;
{{WikiDoc Help Menu}}&lt;br /&gt;
{{WikiDoc Sources}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
	<entry>
		<id>https://www.wikidoc.org/index.php?title=Chondroma_classification&amp;diff=861381</id>
		<title>Chondroma classification</title>
		<link rel="alternate" type="text/html" href="https://www.wikidoc.org/index.php?title=Chondroma_classification&amp;diff=861381"/>
		<updated>2013-03-13T13:42:12Z</updated>

		<summary type="html">&lt;p&gt;Shivali Marketkar: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{Chondroma}}&lt;br /&gt;
{{CMG}};&#039;&#039;&#039;Assistant Editor-in-Chief:&#039;&#039;&#039; Somal Khan&lt;br /&gt;
&lt;br /&gt;
==Overview==&lt;br /&gt;
Chondromas are classified according to their location.&lt;br /&gt;
[[Endochondromas]] : Tumor grows within the bone and expands it.&lt;br /&gt;
[[Ecchondroma]] - grows outward from the bone and this is rare. [[Periosteal]] chondomas are on the surface of the bone and other chondromas form in soft tissues.&lt;br /&gt;
&lt;br /&gt;
==Video==&lt;br /&gt;
{{#ev:youtube|FLqr7Ld5-qc}}&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|2}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Disease]]&lt;br /&gt;
[[Category:Oncology]]&lt;br /&gt;
[[Category:Orthopedics]]&lt;br /&gt;
[[Category:Needs content]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Types of cancer]]&lt;br /&gt;
[[Category:Skeletal disorders]]&lt;br /&gt;
&lt;br /&gt;
{{WikiDoc Help Menu}}&lt;br /&gt;
{{WikiDoc Sources}}&lt;/div&gt;</summary>
		<author><name>Shivali Marketkar</name></author>
	</entry>
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