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Epithelioid sarcoma with retained INI1 expression as a cause of a chronic leg ulcer
T. Maňáková, J. Hojný, M. Sedlář, M. Vočka, K. Chrz, P. Mitáš, J. Beneš, R. Holaj
Language English Country Great Britain
Document type Case Reports
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from 2016-01-01
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- Publication type
- Case Reports MeSH
Epithelioid sarcoma is a rare soft-tissue sarcoma typically presenting itself as a subcutaneous or deep dermal mass in distal portions of the extremities of adolescents and young adults. They are frequently mistaken for ulcers, abscesses, or infected warts resistant to standard medical treatment. Patients often develop multiple local recurrences with subsequent metastases. We report a case of a 66-year-old patient with chronic leg ulcer who died of generalization of an epithelioid sarcoma.
1st Department of Surgery General University Hospital Prague Prague Czech Republic
1st Faculty of Medicine Charles University Prague Prague Czech Republic
2nd Department of Cardiovascular Surgery General University Hospital Prague Prague Czech Republic
3rd Department of Medicine General University Hospital Prague Prague Czech Republic
Department of Oncology General University Hospital Prague Prague Czech Republic
Department of Radiodiagnostics General University Hospital Prague Prague Czech Republic
Institute of Pathology General University Hospital Prague Prague Czech Republic
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- $a Maňáková, Tatjana $u Institute of Pathology, General University Hospital in Prague, Prague, Czech Republic $u 1st Faculty of Medicine, Charles University in Prague, Prague, Czech Republic
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- $a Epithelioid sarcoma is a rare soft-tissue sarcoma typically presenting itself as a subcutaneous or deep dermal mass in distal portions of the extremities of adolescents and young adults. They are frequently mistaken for ulcers, abscesses, or infected warts resistant to standard medical treatment. Patients often develop multiple local recurrences with subsequent metastases. We report a case of a 66-year-old patient with chronic leg ulcer who died of generalization of an epithelioid sarcoma.
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