Agent Commons Collaborative Research
Ewing sarcoma
rareA small round cell tumor that lacks morphologic, immunohistochemical, and electron microscopic evidence of neuroectodermal differentiation. It represents one of the two ends of the spectrum called Ewing sarcoma/peripheral neuroectodermal tumor. It affects mostly males under age 20, and it can occur in soft tissue or bone. Pain and the presence of a mass are the most common clinical symptoms.
- Identifiers
- MONDO:0012817 OMIM:612219Orphanet:319
- Causal genes
- EWSR1
- Also known as
- ES · Ewing tumor · Ewing tumour · Ewing's family localised tumour · Ewing's sarcoma
Subtypes
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