Myxoma pathophysiology: Difference between revisions

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{{Myxoma}}
{{Myxoma}}
{{CMG}} {{AE}} {{CZ}}{{AAM}}{{MV}}
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==Overview==
==Overview==


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==Pathophysiology==
==Pathophysiology==
Cardiac myxoma arises from myxoid collagenous [[stroma]], which is composed of mesenchymal cells that are normally involved in the supportive structure of the tissue.  Myxomas are usually located in the [[endocardium]] of the [[atrial septum]]. Some symptoms of myxoma may be associated with the release of [[interleukin 6]] (IL-6) by the myxoma.<ref name="Seino-IL6">{{cite journal | author=Seino Y, Ikeda U, Shimada K. | title=Increased expression of interleukin 6 mRNA in cardiac myxomas. | journal=Br Heart J | year=1993 | volume=69 | issue=6 | pages=565-7 | id=PMID 8343326}}</ref><ref name="Jourdan-IL6">{{cite journal | author=Jourdan M, Bataille R, Seguin J, Zhang XG, Chaptal PA, Klein B | title=Constitutive production of interleukin-6 and immunologic features in cardiac myxomas.| journal=Arthritis Rheum | year=1990 | volume=33 | issue=3 | pages=398-402 | id=PMID 1690543}}</ref>  
 
Cardiac myxoma arises from remnants of subendocardial vasoformative reserve cells, which are primitive [[mesenchymal]] cells that are normally involved in the supportive structure of the [[endocardium]]. <ref name="pmid10064365">{{cite journal |vauthors=Roscher AA, Kato NS, Quan H, Padmanabhan M |title=Intra-atrial myxomas, clinical-pathologic correlation based on two case studies including historical review |journal=J Cardiovasc Surg (Torino) |volume=37 |issue=6 Suppl 1 |pages=131–7 |year=1996 |pmid=10064365 |doi= |url=}}</ref> <ref name="pmid11737312">{{cite journal |vauthors=Acebo E, Val-Bernal JF, Gómez-Román JJ |title=Prichard's structures of the fossa ovalis are not histogenetically related to cardiac myxoma |journal=Histopathology |volume=39 |issue=5 |pages=529–35 |year=2001 |pmid=11737312 |doi= |url=}}</ref> Myxomas are usually located in the [[fossa ovalis]] and [[endocardium]] of the [[atrial septum]].
 
===Gross Pathology===
===Gross Pathology===


On gross pathology, external appearance, consistency size and weight are extremely variable findings of cardiac myxoma. Large cardiac myxomas are usually located in [[fossa ovalis]] and tend to be sessile or pedunculated. Tumor consistency depends on the quantity and distribution of fibrous tissue and calcification. A macroscopic gelatinous, irregular surface that fills the [[left atrium]] is a characteristic finding of myxoma.
On gross pathology, external appearance, consistency size and weight are extremely variable findings of cardiac myxoma. Tumor consistency depends on the quantity and distribution of fibrous tissue and calcification (It can be smooth, lobulated, friable or gelatinous). <ref name="pmid25297937">{{cite journal |vauthors=Di Vito A, Mignogna C, Donato G |title=The mysterious pathways of cardiac myxomas: a review of histogenesis, pathogenesis and pathology |journal=Histopathology |volume=66 |issue=3 |pages=321–32 |year=2015 |pmid=25297937 |doi=10.1111/his.12531 |url=}}</ref> Usually a macroscopic gelatinous, irregular surface that fills the [[left atrium]] is a characteristic finding of myxoma. Myxomas that have irregular consistency are more likely to form surface thrombi and embolize. 
 
Morphologically, these lesions tend to be attached to the endocardium by a broad-based pedunculated stalk. In some cases, the attachment to the endocardium can also be  without a clear stalk, or sessile. Cardiac myxomas are non-invasive tumors, thus there is no infiltration to underlying tissues.
 
Cardiac myxomas are intracavitary tumors. The distribution is normally within the interatrial septum or adjacent to foramen ovale. However, they can also be found in other cardiac chambers, such as right atrium (15%),ventricles(˜2%)or cardiac valves (rare).<ref name="pmid12208428">{{cite journal |vauthors=Yoon DH, Roberts W |title=Sex distribution in cardiac myxomas |journal=Am. J. Cardiol. |volume=90 |issue=5 |pages=563–5 |year=2002 |pmid=12208428 |doi= |url=}}</ref> Large cardiac myxomas are usually located in [[fossa ovalis]].The average tumor size is from 0.6 to 12 cm, with a mean weight of 40 g.<ref name="pmid10903697">{{cite journal |vauthors=Grebenc ML, Rosado de Christenson ML, Burke AP, Green CE, Galvin JR |title=Primary cardiac and pericardial neoplasms: radiologic-pathologic correlation |journal=Radiographics |volume=20 |issue=4 |pages=1073–103; quiz 1110–1, 1112 |year=2000 |pmid=10903697 |doi=10.1148/radiographics.20.4.g00jl081073 |url=}}</ref>
 
 


[http://www.peir.net Images shown below are courtesy of Professor Peter Anderson DVM PhD and published with permission © PEIR, University of Alabama at Birmingham, Department of Pathology]
[http://www.peir.net Images shown below are courtesy of Professor Peter Anderson DVM PhD and published with permission © PEIR, University of Alabama at Birmingham, Department of Pathology]

Revision as of 15:30, 19 November 2015

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Maria Fernanda Villarreal, M.D. [2]Cafer Zorkun, M.D., Ph.D. [3]Ahmad Al Maradni, M.D. [4]

Overview

Cardiac myxoma contains undifferentiated mesenchymal cells, which potentially differentiate into many tissues such as blood vessels, glandular structures, bones, and source of extramedullary hematopoiesis.[1]

Pathophysiology

Cardiac myxoma arises from remnants of subendocardial vasoformative reserve cells, which are primitive mesenchymal cells that are normally involved in the supportive structure of the endocardium. [2] [3] Myxomas are usually located in the fossa ovalis and endocardium of the atrial septum.

Gross Pathology

On gross pathology, external appearance, consistency size and weight are extremely variable findings of cardiac myxoma. Tumor consistency depends on the quantity and distribution of fibrous tissue and calcification (It can be smooth, lobulated, friable or gelatinous). [4] Usually a macroscopic gelatinous, irregular surface that fills the left atrium is a characteristic finding of myxoma. Myxomas that have irregular consistency are more likely to form surface thrombi and embolize.

Morphologically, these lesions tend to be attached to the endocardium by a broad-based pedunculated stalk. In some cases, the attachment to the endocardium can also be without a clear stalk, or sessile. Cardiac myxomas are non-invasive tumors, thus there is no infiltration to underlying tissues.

Cardiac myxomas are intracavitary tumors. The distribution is normally within the interatrial septum or adjacent to foramen ovale. However, they can also be found in other cardiac chambers, such as right atrium (15%),ventricles(˜2%)or cardiac valves (rare).[5] Large cardiac myxomas are usually located in fossa ovalis.The average tumor size is from 0.6 to 12 cm, with a mean weight of 40 g.[6]


Images shown below are courtesy of Professor Peter Anderson DVM PhD and published with permission © PEIR, University of Alabama at Birmingham, Department of Pathology

Microscopic Pathology

On microscopic histopathological analysis, Gamna-Bodies consist of fibrosis and deposition of iron pigments are characteristic findings of myxoma. Myxoma cells can be elongated, fusiform or stellate. They contain modest amounts of eosinophilic cytoplasm and have oval nuclei.

Images shown below are courtesy of Professor Peter Anderson DVM PhD and published with permission © PEIR, University of Alabama at Birmingham, Department of Pathology

References

  1. Bulkley BH, Hutchins GM (1979). "Atrial myxomas: a fifty year review". Am. Heart J. 97 (5): 639–43. PMID 433739.
  2. Roscher AA, Kato NS, Quan H, Padmanabhan M (1996). "Intra-atrial myxomas, clinical-pathologic correlation based on two case studies including historical review". J Cardiovasc Surg (Torino). 37 (6 Suppl 1): 131–7. PMID 10064365.
  3. Acebo E, Val-Bernal JF, Gómez-Román JJ (2001). "Prichard's structures of the fossa ovalis are not histogenetically related to cardiac myxoma". Histopathology. 39 (5): 529–35. PMID 11737312.
  4. Di Vito A, Mignogna C, Donato G (2015). "The mysterious pathways of cardiac myxomas: a review of histogenesis, pathogenesis and pathology". Histopathology. 66 (3): 321–32. doi:10.1111/his.12531. PMID 25297937.
  5. Yoon DH, Roberts W (2002). "Sex distribution in cardiac myxomas". Am. J. Cardiol. 90 (5): 563–5. PMID 12208428.
  6. Grebenc ML, Rosado de Christenson ML, Burke AP, Green CE, Galvin JR (2000). "Primary cardiac and pericardial neoplasms: radiologic-pathologic correlation". Radiographics. 20 (4): 1073–103, quiz 1110–1, 1112. doi:10.1148/radiographics.20.4.g00jl081073. PMID 10903697.


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