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Epithelioid sarcoma

MONDO:0017387

An 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).

Also known as: ES, epithelioid cell sarcoma, epithelioid sarcoma

2827 clinical trials for this condition and its sub-types, 20 tagged with Epithelioid sarcoma itself.

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