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Pleomorphic rhabdomyosarcoma

MONDO:0017386

An aggressive malignant mesenchymal neoplasm with skeletal muscle differentiation, occurring in adults and rarely in children. The tumor is characterized by the presence of bizarre round, spindle, and polygonal cells. Clinical presentation includes a rapidly enlarging painful mass usually of the lower extremities.

Also known as: pleomorphic rhabdomyosarcoma

2818 clinical trials for this condition and its sub-types, 7 tagged with Pleomorphic rhabdomyosarcoma itself.

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Sub-types of Pleomorphic rhabdomyosarcoma

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Showing the 400 most recently updated of 1260 trials in this tab.