Cardiac Epithelioid PEComa: Report of Two Cases and Review of the Literature
Cardiac PEComa is very rare. We reported two cases of epithelioid PEComas, one in an adult and one in a 2-year-old child. Both tumors were composed of sheets of epithelioid cells with coagulation necrosis. In addition, the adult case showed marked nuclear atypia and high mitotic activity with atypic...
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Series: | Case Reports in Medicine |
Online Access: | http://dx.doi.org/10.1155/2012/521678 |
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doaj-fd84e90461544994a258e9fdde8b58182020-11-25T00:08:18ZengHindawi LimitedCase Reports in Medicine1687-96271687-96352012-01-01201210.1155/2012/521678521678Cardiac Epithelioid PEComa: Report of Two Cases and Review of the LiteratureHuilin Niu0F. W. Wang1Paul J. Zhang2Zhanyong Bing3Department of Pathology, Guangzhou Children’s Hospital, Guangzhou 510120, ChinaDepartment of Pathology, Guangzhou Children’s Hospital, Guangzhou 510120, ChinaDepartment of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, 3400 Spruce Street, Philadelphia, PA 19104, USADepartment of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, 3400 Spruce Street, Philadelphia, PA 19104, USACardiac PEComa is very rare. We reported two cases of epithelioid PEComas, one in an adult and one in a 2-year-old child. Both tumors were composed of sheets of epithelioid cells with coagulation necrosis. In addition, the adult case showed marked nuclear atypia and high mitotic activity with atypical mitosis and the pediatric case showed unusual clear cell features. Immunohistochemically, both tumors were positive for HMB-45 and SMA and negative for S100 and cytokeratin. Electron microscopy was performed in the pediatric case and showed premelanosomes. The adult patient developed extensive metastasis indicating malignant behavior. Prior to the two cases, only 5 other cases of cardiac PEComa were reported and the literatures are reviewed.http://dx.doi.org/10.1155/2012/521678 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Huilin Niu F. W. Wang Paul J. Zhang Zhanyong Bing |
spellingShingle |
Huilin Niu F. W. Wang Paul J. Zhang Zhanyong Bing Cardiac Epithelioid PEComa: Report of Two Cases and Review of the Literature Case Reports in Medicine |
author_facet |
Huilin Niu F. W. Wang Paul J. Zhang Zhanyong Bing |
author_sort |
Huilin Niu |
title |
Cardiac Epithelioid PEComa: Report of Two Cases and Review of the Literature |
title_short |
Cardiac Epithelioid PEComa: Report of Two Cases and Review of the Literature |
title_full |
Cardiac Epithelioid PEComa: Report of Two Cases and Review of the Literature |
title_fullStr |
Cardiac Epithelioid PEComa: Report of Two Cases and Review of the Literature |
title_full_unstemmed |
Cardiac Epithelioid PEComa: Report of Two Cases and Review of the Literature |
title_sort |
cardiac epithelioid pecoma: report of two cases and review of the literature |
publisher |
Hindawi Limited |
series |
Case Reports in Medicine |
issn |
1687-9627 1687-9635 |
publishDate |
2012-01-01 |
description |
Cardiac PEComa is very rare. We reported two cases of epithelioid PEComas, one in an adult and one in a 2-year-old child. Both tumors were composed of sheets of epithelioid cells with coagulation necrosis. In addition, the adult case showed marked nuclear atypia and high mitotic activity with atypical mitosis and the pediatric case showed unusual clear cell features. Immunohistochemically, both tumors were positive for HMB-45 and SMA and negative for S100 and cytokeratin. Electron microscopy was performed in the pediatric case and showed premelanosomes. The adult patient developed extensive metastasis indicating malignant behavior. Prior to the two cases, only 5 other cases of cardiac PEComa were reported and the literatures are reviewed. |
url |
http://dx.doi.org/10.1155/2012/521678 |
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