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Updated: Jun 23, 2025

Teratoma Generation in the Testis Capsule
Published on: November 7, 2011
Testicular juvenile granulosa cell tumor: a case report
Michelangelo Baldazzi1, Eugenio Rossi2, Rocco Minelli3
1Pediatric and Adult CardioThoracic and Vascular, Oncohematologic and Emergency Radiology Unit, IRCCS Azienda Ospedaliero-Universitaria Di Bologna, Bologna, Italy. michelangelo.baldazzi@gmail.com.
Abstract:
The Testicular Juvenile Granulosa Cell Tumor (JGCT) is a rare testicular neoplasm that appears in the first months of life as a painless testicular mass. Following an accurate radiological ultrasound diagnosis, through which the cystic appearance of the lesion is observed, and histological confirmation, showing follicular growth pattern and an immunoreactivity for inhibin, the treatment process involves, when feasible, conservative surgery. We present the case of a 2-months old infant with a bilateral JGCT of the testis and we review the classical findings of the patology.
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