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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease soft tissue sarcoma
Comorbidity C0279980|extraskeletal ewing\'s sarcoma
Sentences 4
PubMedID- 23346500 Extraskeletal ewing's sarcoma (es) is a small round cell tumor that occurs in extraskelectal tissue.
PubMedID- 22933997 Reported cases of extraskeletal ewing's sarcoma of the spine in the pediatric [1, 2, 3] and adult [1, 4, 5] populations have been documented.
PubMedID- 22937369 It is classified along with extraskeletal ewing's sarcoma, askin's tumour, and peripheral neuroectodermal tumour (pnet) into ewing's family of tumours, first described by ewing in 1921 [1].
PubMedID- 20871855 Extraskeletal ewing's sarcoma (ees) is a rare type of ewing's sarcoma that arises in the soft tissue at any location and is now regarded as a member of a family of small cell neoplasms of bone and soft tissue, including primitive neuroectodermal tumors (pnets) [1, 2].multimodal treatment combined with surgical treatment, chemotherapy, and radiotherapy (rt) contributes the improvements of clinical outcomes in ees [3].

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