Hamartoma: Difference between revisions

	Hamartoma Microchapters
Home
Patient Information
Overview
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Hamartoma from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
Diagnostic Study of Choice
Staging
History and Symptoms
Physical Examination
Laboratory Findings
Electrocardiogram
Chest X Ray
CT
MRI
Ultrasound
Other Imaging Findings
Other Diagnostic Studies
Treatment
Medical Therapy
Surgery
Primary Prevention
Secondary Prevention
Cost-Effectiveness of Therapy
Future or Investigational Therapies
Case Studies
Case #1
Hamartoma On the Web
Most recent articles
Most cited articles
Review articles
CME Programs
Powerpoint slides
Images
American Roentgen Ray Society Images of Hamartoma All Images X-rays Echo & Ultrasound CT Images MRI
Ongoing Trials at Clinical Trials.gov
US National Guidelines Clearinghouse
NICE Guidance
FDA on Hamartoma
CDC on Hamartoma
Hamartoma in the news
Blogs on Hamartoma
Directions to Hospitals Treating Hamartoma
Risk calculators and risk factors for Hamartoma

	Hamartoma;
	Hamartoma of the spleen. The hamartoma is the dark circular object on the left that dominates the image. This is a cross-section, the growth being about 9 cm in diameter, while the spleen is actually about 11 cm. ; (Courtesy of Ed Uthman, MD)

VisualWikitext

Latest revision as of 14:38, 28 February 2019

For patient information, click here

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] ; Associate Editor(s)-in-Chief: Vamsikrishna Gunnam M.B.B.S [2] Maria Fernanda Villarreal, M.D. [3]

Synonyms and keywords: Hamartomatosis; Hamartomatous disease; Hamartoses; Pulmonary hamartoma; Tuber cinereum hamartoma; Splenic hamartoma; Cardiac fibroma

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Hamartoma from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Treatment

Case Studies

Case#1

Template:Tumors Template:Phakomatoses and other congenital malformations not elsewhere classified

de:Hamartom hu:Hamartoma

Template:WikiDoc Sources

@@ Line 1: / Line 1: @@
+__NOTOC__
+'''For patient information, click [[Hamartoma (patient information)|here]]'''
 {{Infobox_Disease |
    Name           = {{PAGENAME}} |
    Image          = spleen2.jpg|
    Caption        = ''Hamartoma of the spleen.'' The hamartoma is the dark circular object on the left that dominates the image. This is a cross-section, the growth being about 9 cm in diameter, while the spleen is actually about 11 cm. <br> (Courtesy of Ed Uthman, MD) |
-  DiseasesDB     = 19785 |
-  ICD10          = {{ICD10|Q|85|9|q|80}} |
-  ICD9           = {{ICD9|757.32}}, {{ICD9|759.6}} |
-  ICDO           = |
-  OMIM           = |
-  MedlinePlus    = |
-  eMedicineSubj  = |
-  eMedicineTopic = |
-  MeshID         = D006222 |
 }}
-{{Search infobox}}
+{{Hamartoma}}
-{{CMG}}
+{{CMG}} ; {{AE}} {{VKG}} {{MV}}
-{{EH}}
+{{SK}} Hamartomatosis; Hamartomatous disease; Hamartoses; Pulmonary hamartoma; Tuber cinereum hamartoma; Splenic hamartoma; Cardiac fibroma
-==Overview==
+==[[Hamartoma overview|Overview]]==
-A '''hamartoma''' is a focal malformation that resembles a neoplasm in the tissue of its origin.  This is not a malignant tumor, and it grows at the same rate as the surrounding tissues. It is composed of tissue elements normally found at that site but that are growing in a disorganized mass. They occur in many different parts of the body and are most often asymptomatic and undetected unless seen on an image taken for another reason.  Hamartomas result from an abnormal formation of normal tissue, although the underlying reasons for the abnormality are not fully understood.  They grow along with, and at the same rate as, the organ from whose tissue they are made, and, unlike cancerous tumors, only rarely invade or compress surrounding structures significantly.
+==[[Hamartoma historical perspective|Historical Perspective]]==
-A hamartoma, while generally benign, can cause problems due to their location.  When located on the skin, especially the face or neck, they can be extremely disfiguring, as in the case of a man with a hamartoma the size of a small orange on his eyelid.<ref>http://dermatlas.med.jhmi.edu/derm/IndexDisplay.cfm?ImageID=2040682463</ref>  They may obstruct practically any organ in the body, such as the eye, the colon, etc.  They are particularly likely to cause major health issues when located in the hypothalamus, spleen or kidneys.
+==[[Hamartoma classification|Classification]]==
-==Lung==
+==[[Hamartoma pathophysiology|Pathophysiology]]==
-'''The most common hamartomas occur in the lungs'''. About 5-8% of all solitary lung tumors, about 75% of all '''[[benign]]''' lung tumors are hamartomas.  They almost always arise from connective tissue and are generally formed of cartilage, fat, and connective tissue cells, although they may include many other types of cells. The great majority of them form in the connective tissue on the outside of the lungs, although about 10% form deep in the linings of the bronchii.  They can be worrisome, especially if situated deep in the lung, as it is important and sometimes difficult to distinguish them from malignancies.  An x-ray will often not provide definitive diagnosis, and even a CAT scan may be insufficient if the hamartoma atypically lacks cartilage and fat cells.  Lung hamartomas are more common in men than in women and may present additional difficulties in smokers.
-Some lung hamartomas can compress surrounding lung tissue to a degree, but this is generally not debilitative or even noticed by the patient, especially for the more common peripheral growths.  They are treated, if at all, by surgical resection, with an excellent prognosis:  generally, the only real danger is the inherent possibility of surgical complications.
+==[[Hamartoma causes|Causes]]==
-==Heart==
+==[[Hamartoma differential diagnosis|Differentiating Hamartoma from other Diseases]]==
-Cardiac rhabdomyomas are hamartomas comprised of altered cardiac myocytes that contain large vacuoles and glycogen. They are the second most common tumor of the heart in children and infants (after fibromas). There is a strong association between cardiac rhabdomyomas and tuberous sclerosis (characterized by hamartomas of the central nervous system, kidneys and skin, as well as pancreatic cysts; 25-50% of patients with cardiac rhabdomyomas will have [[tuberous sclerosis]], and up to 100% of patients with tuberous sclerosis will have cardiac masses by echocardiography.  Symptoms depend on the size of the tumor, its location relative to the conduction system, and whether it obstructs blood flow.  Symptoms are usually from congestive heart failure (in utero heart failure may occur).  If patients survive infancy, their tumors may regress spontaneously; resection in symptomatic patients has good results.
-==[[Hypothalamus]]==
+==[[Hamartoma epidemiology and demographics|Epidemiology and Demographics]]==
-One of the most troublesome hamartomas occurs on the hypothalamus.  Unlike most such growths, a [[hypothalamic hamartoma]] is symptomatic; ''' it most often causes [[gelastic]] seizures''', and can cause visual problems, other seizures, rage disorders associated with hypothalamic diseases, and early onset of puberty.  The symptoms typically begin in early infancy and are progressive, often into general cognitive and/or functional disability.  Moreover, resection is usually difficult, as the growths are generally adjacent to, or even intertwined with, the optic nerve;  however, the symptoms are resistant to medical control.  Luckily, surgical techniques are improving and can result in immense improvement of prognosis. <ref> http://www.emergemd.com/bniq2/article.asp?article_ref_id=20-1-1 Barrow Neurological Institute </ref>
-==Kidneys, spleen, and other vascular organs==
+==[[Hamartoma epidemiology and demographics|Risk Factors]]==
-One general danger of hamartoma is that they may impinge into blood vessels, resulting in a risk of serious bleeding.  Because hamartoma typically lacks elastic tissue, it may lead to the formation of aneurysms and thus possible hemorrhage.  Where a hamartoma impinges into a major blood vessel, such as the renal artery, hemorrhage must be considered life-threatening.
+==[[Hamartoma screening|Screening]]==
-'''Hamartoma of the kidney is also called [[angiomyolipoma]] and can be associated with [[tuberous sclerosis]].'''  It is one of the more frequently seen hamartomas. The condition is more prevalent in women than men, and generally occurs in the right kidney.  Hamartomas of the spleen are uncommon, but can be dangerous.  About 50% of such cases manifest abdominal pain and they  are often associated with hematologic abnormalities and spontaneous rupture.
+==[[Hamartoma natural history|Natural History, Complications and Prognosis]]==
-Angiomyolipoma is not a hamartoma by definition, because fat and smooth muscles are not normal constituents of renal parenchyma. It is a Choristoma (microscopically normal cells or tissues in abnormal locations).
+==Diagnosis==
+[[Hamartoma diagnostic study of choice|Diagnostic Study of Choice]] | [[Hamartoma staging|Staging]] | [[Hamartoma history and symptoms|History and Symptoms]] | [[Hamartoma physical examination|Physical Examination]] | [[Hamartoma laboratory tests|Laboratory Findings]] | [[Hamartoma electrocardiogram|Electrocardiogram]] | [[Hamartoma chest x ray|Chest X Ray]] | [[Hamartoma CT|CT]] | [[Hamartoma MRI|MRI]] | [[Hamartoma ultrasound|Ultrasound]] | [[Hamartoma other imaging findings|Other Imaging Findings]] | [[Hamartoma other diagnostic studies|Other Diagnostic Studies]]
-==[[Cowden syndrome]]==
+==Treatment==
+[[Hamartoma medical therapy|Medical Therapy]] | [[Hamartoma surgery|Surgery]] | [[Hamartoma primary prevention|Primary Prevention]] | [[Hamartoma secondary prevention|Secondary Prevention]] | [[Hamartoma cost-effectiveness of therapy|Cost-Effectiveness of Therapy]] | [[Hamartoma future or investigational therapies|Future or Investigational Therapies]]
-'''''Cowden Syndrome'' or ''Cowden Disease'' is a serious genetic disorder <ref> Mutation of PTEN gene on arm 10q or rarely germline mutation in BMPR1A </ref> characterized by multiple hamartomas.  Usually skin hamartomas exist, and commonly (about 66% of cases) hamartoma of the thyroid gland exists'''.  Additional growths can form in many parts of the body, especially in mucosa, the GI tract, bones, CNS, the eyes, and the genourinary tract.  The hamartomas themselves may cause symptoms or even death, but morbidity is more often associated with increased occurrence of malignancies, usually in the breast or thyroid.
-==References==
-<references/>
-==External links==
-* [http://www.emedicine.com/radio/topic316.htm eMedicine - "Lung Hamartoma"]
-* [http://www.emedicine.com/radio/topic28.htm eMedicine - "Angiomyolipoma"]
-* {{DermAtlas|8}}
+==Case Studies==
+[[Hamartoma case study one|Case#1]]
 {{Tumors}}
 {{Phakomatoses and other congenital malformations not elsewhere classified}}
-{{SIB}}
 [[Category:Anatomical pathology]]
+[[Category:Disease]]
+[[Category:Types of cancer]]
 [[Category:Oncology]]
-[[Category:Pulmonology]]
 [[de:Hamartom]]
@@ Line 76: / Line 61: @@
 {{WikiDoc Help Menu}}
 {{WikiDoc Sources}}
+ [[Category:Up-To-Date]]
+[[Category:Oncology]]
+[[Category:Medicine]]
+[[Category:Surgery]]


Hamartoma
Hamartoma of the spleen. The hamartoma is the dark circular object on the left that dominates the image. This is a cross-section, the growth being about 9 cm in diameter, while the spleen is actually about 11 cm. (Courtesy of Ed Uthman, MD)

Hamartoma: Difference between revisions

Latest revision as of 14:38, 28 February 2019

Diagnosis

Treatment

Case Studies

Navigation menu