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- W2040881903 endingPage "126" @default.
- W2040881903 startingPage "108" @default.
- W2040881903 abstract "Ewing sarcoma/peripheral primitive neuroectodermal tumor (EWS/pPNET) and other tumors with EWS gene rearrangements encompass a malignant and intermediate neoplasm with a broad anatomic distribution and a wide age range but a predilection for soft tissue in children, adolescents, and young adults. The overlapping histologic, immunohistochemical and cytogenetic and molecular genetic features create diagnostic challenges despite significant clinical and prognostic differences. Ewing sarcoma is the 3rd most common sarcoma in children and adolescents, and desmoplastic small round cell tumor is a rare neoplasm that occurs more often in older children, adolescents, and young adults. Pathologic examination is complemented by immunohistochemistry, cytogenetics, and molecular genetics. This article reviews the clinicopathologic features of EWS/pPNET and desmoplastic small round cell tumor in the spectrum of tumors with EWS gene rearrangements. Other tumors with different histopathologic features and an EWS gene rearrangement are discussed elsewhere in this volume." @default.
- W2040881903 created "2016-06-24" @default.
- W2040881903 creator A5015423699 @default.
- W2040881903 creator A5019491571 @default.
- W2040881903 creator A5049058632 @default.
- W2040881903 creator A5059497696 @default.
- W2040881903 date "2012-01-01" @default.
- W2040881903 modified "2023-10-15" @default.
- W2040881903 title "Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor and Related Tumors" @default.
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