loading...| Preferred Name | Ewing sarcoma/peripheral primitive neuroectodermal tumor | |
| Synonyms |
Ewing family of tumours Ewing sarcoma family of tumors Ewing sarcoma family of tumours Ewing sarcoma/peripheral primitive neuroectodermal tumor Ewing sarcoma/peripheral PNET Ewing's family of tumours Ewing family of tumors Ewing's sarcoma/peripheral primitive neuroectodermal tumor Ewing's sarcoma/peripheral primitive neuroectodermal tumour tumours of Ewing's family tumors of the Ewing's family tumours of the Ewing's family tumors of Ewing's family Ewing's family of tumors EFTs |
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| Definitions |
A spectrum of malignant tumors, affecting mostly males under age 20, 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. These tumors may occur in the soft tissues or the bones. Pain and the presence of a mass are the most common clinical symptoms. |
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| ID |
http://purl.obolibrary.org/obo/MONDO_0021038 |
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| database_cross_reference |
NCIT:C27291 UMLS:C3536893 MEDGEN:760735 |
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| definition |
A spectrum of malignant tumors, affecting mostly males under age 20, 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. These tumors may occur in the soft tissues or the bones. Pain and the presence of a mass are the most common clinical symptoms. |
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| has_exact_synonym |
Ewing family of tumours Ewing sarcoma family of tumors Ewing sarcoma family of tumours Ewing sarcoma/peripheral primitive neuroectodermal tumor Ewing sarcoma/peripheral PNET Ewing's family of tumours Ewing family of tumors Ewing's sarcoma/peripheral primitive neuroectodermal tumor Ewing's sarcoma/peripheral primitive neuroectodermal tumour tumours of Ewing's family tumors of the Ewing's family tumours of the Ewing's family tumors of Ewing's family Ewing's family of tumors EFTs |
|
| id |
MONDO:0021038 |
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| in_subset | ||
| label |
Ewing sarcoma/peripheral primitive neuroectodermal tumor |
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| notation |
MONDO:0021038 |
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| preferred label |
Ewing sarcoma/peripheral primitive neuroectodermal tumor |
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| prefLabel |
Ewing sarcoma/peripheral primitive neuroectodermal tumor |
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| skos_exactMatch |
http://identifiers.org/medgen/760735 |
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| subClassOf |