extraskeletal Ewing sarcoma/peripheral primitive neuroectodermal tumor
http://purl.obolibrary.org/obo/MONDO_0021039
A spectrum of malignant tumors arising from the soft tissues, characterized morphologically by the presence of small round cells. Ewing sarcoma and peripheral primitive neuroectodermal tumor represent the ends of a spectrum, with Ewing sarcoma lacking evidence of neural differentiation and the markers that characterize the peripheral primitive neuroectodermal tumor. Ewing sarcoma and peripheral primitive neuroectodermal tumor may share cytogenetic abnormalities, proto-oncogene expression, cell culture and immunohistochemical abnormalities. Pain and the presence of a mass are the most common clinical symptoms. [ NCIT:C27293 ]
Term info
- UMLS:C1333514 (NCIT:C27293)
- DOID:4985 (MONDO:equivalentTo)
- EFO:1000250 (MONDO:equivalentTo)
- NCIT:C27293 (MONDO:equivalentTo)
A spectrum of malignant tumors arising from the soft tissues, characterized morphologically by the presence of small round cells. Ewing sarcoma and peripheral primitive neuroectodermal tumor represent the ends of a spectrum, with Ewing sarcoma lacking evidence of neural differentiation and the markers that characterize the peripheral primitive neuroectodermal tumor. Ewing sarcoma and peripheral primitive neuroectodermal tumor may share cytogenetic abnormalities, proto-oncogene expression, cell culture and immunohistochemical abnormalities. Pain and the presence of a mass are the most common clinical symptoms.
http://linkedlifedata.com/resource/umls/id/C1333514, http://purl.obolibrary.org/obo/DOID_4985, http://purl.obolibrary.org/obo/NCIT_C27293
extraosseous Ewings sarcoma-primitive neuroepithelial tumor, extraosseous Ewing's sarcoma/peripheral primitive neuroectodermal tumor, extraskeletal Ewing sarcoma/peripheral primitive neuroectodermal tumor, extraosseous Ewing sarcoma/peripheral primitive neuroectodermal tumor
extraosseous Ewing's tumor
MONDO:0021039