Poorly Differentiated Ovarian Sertoli-Leydig Cell Tumor in a 16-Year-Old Single Woman: A Case Report and Literature Review

Author:

Abu-Zaid Ahmed1ORCID,Azzam Ayman2ORCID,Alghuneim Lama Abdulhamid1ORCID,Metawee Mona Tarek1ORCID,Amin Tarek3ORCID,Al-Hussain Turki Omar4

Affiliation:

1. College of Medicine, Alfaisal University, P.O. Box 50927, Riyadh 11533, Saudi Arabia

2. Department of General Surgery, Faculty of Medicine, Alexandria University, Alexandria 21526, Egypt

3. Department of Surgical Oncology, King Faisal Specialist Hospital and Research Center (KFSH&RC), P.O. Box 3354, Riyadh 11211, Saudi Arabia

4. Department of Pathology and Laboratory Medicine, King Faisal Specialist Hospital and Research Center (KFSH&RC), P.O. Box 3354, Riyadh 11211, Saudi Arabia

Abstract

Sertoli-Leydig cell tumor (SLCT) of ovary is an exceedingly unusual neoplasm that belongs to a group of sex cord-stromal tumors of ovary and accounts for less than 0.5% of all primary ovarian neoplasms. Very few case reports have been documented in the literature so far. Herein, we report a case of primary poorly differentiated ovarian Sertoli-Leydig cell tumor (SLCT) involving the left ovary in a 16-year-old single woman who presented with a 3-month history of a pelviabdominal mass, acne, hirsutism, and menstrual irregularities. In addition, a literature review on ovarian SLCTs is provided.

Publisher

Hindawi Limited

Subject

Obstetrics and Gynaecology

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