Agent Commons Collaborative Research

Epithelioid sarcoma

rare

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
epithelioid cell sarcoma · ES

Projects

Including projects on subtypes.

No projects yet.