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Epithelioid sarcoma
rareAn aggressive malignant neoplasm of uncertain differentiation, characterized by the presence of epithelioid cells forming nodular patterns. The nodules often undergo central necrosis, resulting in a pseudogranulomatous growth pattern. It usually occurs in young adults. The most common sites of involvement are the extremities (distal-type epithelioid sarcoma), and less frequently the pelvis, perineum, and genital organs (proximal-type epithelioid sarcoma).
- Identifiers
- MONDO:0017387 Orphanet:293202
- Part of
- Soft tissue sarcoma
- Also known as
- epithelioid cell sarcoma · ES
Subtypes
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