Extraovarian granulosa cell tumor: A case report

Authors

DOI:

https://doi.org/10.28982/josam.560112

Keywords:

Extraovarian, Granulosa cell tumor, Histological diagnosis

Abstract

Granulosa cell tumor (GCT) of the ovary is a rare tumor representing 2 to 5% of all ovarian neoplasms. It can reproduce or metastasize several years after the initial treatment. In rare cases, CGT can develop on an extra-ovarian site, which is thought to originate from ectopic gonadal tissue along the embryonic genital ridge. We herein present a case of extraovarian granulosa tumor, the clinical and therapeutic aspects, and our approach.

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References

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Published

2019-10-01

Issue

Section

Case Report

How to Cite

1.
El Marouni A, Aziz K, Toghrai İmane, Mazaz K, Ibn Majdoub K. Extraovarian granulosa cell tumor: A case report. J Surg Med [Internet]. 2019 Oct. 1 [cited 2022 Jun. 25];3(10):772-3. Available from: https://jsurgmed.com/article/view/560112

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