Ewing sarcoma

MONDO:0012817

A 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.

Also known as: ES, Ewing sarcoma, Ewing's family localised tumour, Ewing's sarcoma, Ewing's tumor, Ewing's tumour, Ewing tumor, Ewing tumour

2592 clinical trials for this condition and its sub-types.

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