A RARE CASE REPOT: JUVENILE GRANULOSA CELL TUMOUR

Authors

  • Ruby Rao SHKM Govt. Medical College, Nalhar Haryana

Abstract

ABSTRACT:

Ovarian cancer is the third most common neoplasm of the female genital tract. Based on the cell type of origin, primary ovarian malignancies are classified into surface epithelium, germ cell, and sex cord tumors. Sex cord tumors account for 1% to 2% of ovarian malignancies. Juvenile Granulosa Cell Tumours (JGCTs) are clinically & histopathologically distinct from the GCTs. They are rarely encountered but mostly in youngsters. Surgery is the primary modality of treatment with chemotherapy being reserved for advanced or recurrent disease states. We herewith report an interesting case of JGCT in a young teenage girl.

Keywords: Ovarian sex cord stromal tumours, Juvenile granulosa cell tumour

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Published

2019-02-27

How to Cite

Ruby Rao. (2019). A RARE CASE REPOT: JUVENILE GRANULOSA CELL TUMOUR. International Journal of Medical Science And Diagnosis Research, 3(2). Retrieved from https://ijmsdr.com/index.php/ijmsdr/article/view/257

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Articles