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Juvenile granulosa cell tumor of the testis: prenatal diagnosis and prescrotal approach

DOI: 10.1186/1824-7288-38-67

Keywords: Gonadal sex cord stromal tumor , Orchiectomy , Alpha fetoprotein , Ultrasound , Human chorionic gonadotropin

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Abstract:

Neonatal testicular tumors are rare and should be considered in the differential diagnosis of newborn scrotal masses. Juvenile granulosa cell tumor (JGCT) accounts for about 5% of all prepubertal testis tumors. As a benign neoplasm, radical orchiectomy is sufficient for treatment. We report a case of a newborn with a prenatal diagnosis of scrotal mass. After surgery, the histological diagnosis was juvenile granulosa cell tumor. To date the patient is healthy.

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