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Rhabdoid tumor

MONDO:0002728

An aggressive malignant embryonal neoplasm usually occurring during childhood. It is characterized by the presence of large cells with abundant cytoplasm, large eccentric nucleus, and a prominent nucleolus and it is associated with abnormalities of chromosome 22. It can arise from the central nervous system, kidney, and the soft tissues. The prognosis is poor.

Also known as: malignant rhabdoid tumor, rhabdoid sarcoma, rhabdoid tumor, rhabdoid cancer

2894 clinical trials for this condition and its sub-types, 63 tagged with Rhabdoid tumor itself.

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