RESUMO
Juvenile granulosa cell tumor [JGCT] is a rarely diagnosed subset of benign sex cord-stromal testis tumors. Although it accounts for only 1.2% of all prepubertal testis tumors, the JGCT is one of the most common congenital and infantile testicular neoplasms. In contrast to other sex cord-stromal tumors in boys and to the ovarian homologue of the JCGT, there are no clinically evident endocrine manifestations. In this article we report a case of juvenile granulosa cell tumor of the left testis ina 3-month-old infant
RESUMO
Juvenile granulosa cell tumor [JGCT] is one of the rare sex cord-stromal tumours of the ovary occurring in the first two decades of life .It makes less than 5% of ovarian tumours in childhood and adolescence
It is different from adult granulosa cell tumor that is seen in older females with respect to clinical and pathological features as well as biological behaviour. In this article we report a case of juvenile granulosa cell tumor of the right ovary in a 7-month-old infant which was presented with vaginal bleeding