Jinekoloji ve Obstetrik Dergisi, cilt.18, sa.3, ss.173-175, 2004 (Scopus)
Juvenile granulosa cell tumor is a variant of granulosa cell tumor and is rarely seen. It manifests itself in the first two decades of life, with characteristic histological features. Only the clinical stage at the time of diagnosis is believed to be of prognostic significance. In this case report, we have presented a 14-years-old girl with ovarian juvenile granulosa cell tumor by reviewing the relevant literature. Recurrence of tumor has not been accured in three years.