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 immunoreactivity for inhibin, the treatment process involves, when feasible, conservative surgery. We present the case of a 2-month-old infant with a bilateral JGCT of the testis and we review the classical findings of the patology.
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