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Rhabdoid tumor
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.
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Atypical teratoid rhabdoid tumor 35 trials · 36 incl. sub-types Sub-types →
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Rhabdoid tumor of the kidney 7 trials
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Extrarenal rhabdoid tumor 1 trial
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Familial rhabdoid tumor 0 trials · 1 incl. sub-types Sub-types →
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Striated muscle rhabdoid tumor 0 trials