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Poorly Differentiated Ovarian Sertoli-Leydig Cell Tumor in a 16-Year-Old Single Woman: A Case Report and Literature Review
Author(s) -
Ahmed AbuZaid,
Ayman Azzam,
Lama Abdulhamid Alghuneim,
Mona Metawee,
Tarek Amin,
Turki AlHussain
Publication year - 2013
Publication title -
case reports in obstetrics and gynecology
Language(s) - English
Resource type - Journals
eISSN - 2090-6684
pISSN - 2090-6692
DOI - 10.1155/2013/858501
Subject(s) - ovary , hirsutism , medicine , neoplasm , ovarian tumor , leydig cell , stromal cell , granulosa cell , leydig cell tumor , gynecology , pathology , hormone , ovarian cancer , luteinizing hormone , insulin resistance , polycystic ovary , cancer , obesity
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.

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