Juvenile granulosa cell tumour of ovary: a casr report

Authors

Dr. Sayani Das, Dr. Palash Mazumder, Dr Shyamali Dutta, Dr Kajal Kumar Patra Author

Keywords:

Juvenile Granulosa Cell Tumor, Ovarian Neoplasm, Pediatric Gynecology, Inhibin B, Pseudo-precocious Puberty, Oophorectomy

Abstract

Juvenile Granulosa Cell Tumor (JGCT) is a rare ovarian neoplasm occurring
predominantly in children and adolescents. We report a case of a 5-year-old girl
presenting with abdominal pain, early satiety, and vaginal bleeding. Imaging revealed
a large solid-cystic ovarian mass, with elevated serum Inhibin B and CA-125 levels.
The patient underwent left salpingo-oophorectomy and infra-colic omentectomy.
Histopathological examination confirmed JGCT. Early diagnosis and surgical
management are key to a good prognosis. Regular follow-up is essential due to the
tumor’s potential for delayed recurrence.