Juvenile type testicular granulosa cell tumor

A rare sex cord-stromal tumor that arises from the testis. It is the most frequent congenital testicular neoplasm and is usually diagnosed during the perinatal period. It usually presents as an asymptomatic scrotal or abdominal mass. Morphologically it is characterized by the presence of cysts that are lined by cells resembling granulosa and theca cells.

Also known as: juvenile granulosa cell tumor, juvenile granulosa cell tumor (morphologic abnormality), juvenile granulosa cell tumour, juvenile granulosa cell tumour (morphologic abnormality), juvenile type granulosa cell neoplasm, juvenile type granulosa cell tumor, juvenile type granulosa cell tumour

1433 clinical trials for this condition and its sub-types, 0 tagged with Juvenile type testicular granulosa cell tumor itself.