| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 3181486 | Actas Dermo-Sifiliográficas | 2008 | 5 Pages | 
Abstract
												Peripheral primitive neuroectodermal tumors-also known as Ewing sarcomas-are a rare type of malignant tumor the histology of which characteristically reveals the presence of small round cells. Typically, t(11;22) translocation is observed. We describe the case of a 45-year-old man with a subcutaneous peripheral primitive neuroectodermal tumor in which the t(11;22) translocation was detected. He was satisfactorily treated with surgery and radiotherapy.
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											Authors
												R. Cabrera, P. Sánchez, M.A. RodrÃguez, 
											