Abu-Zaid Ahmed, Azzam Ayman, Alghuneim Lama Abdulhamid, Metawee Mona Tarek, Amin Tarek, Al-Hussain Turki Omar
College of Medicine, Alfaisal University, P.O. Box 50927, Riyadh 11533, Saudi Arabia.
Case Rep Obstet Gynecol. 2013;2013:858501. doi: 10.1155/2013/858501. Epub 2013 Jun 25.
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.
卵巢支持-间质细胞瘤(SLCT)是一种极为罕见的肿瘤,属于卵巢性索间质肿瘤,占所有原发性卵巢肿瘤的比例不到0.5%。迄今为止,文献中记载的病例报告极少。在此,我们报告一例16岁单身女性的原发性低分化卵巢支持-间质细胞瘤(SLCT),该肿瘤累及左卵巢,患者有3个月盆腔腹部肿块、痤疮、多毛症及月经不规律的病史。此外,还提供了关于卵巢SLCT的文献综述。