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Roth, L.M., Slayton, R.E., Brady, L.W., Blessing, J.A. and Johnson, G. (1985) Retiform Differentiation in Ovarian Sertoli-Leydig Cell Tumors: A Clinicopathologic Study of Six Cases from a Gynecologic Oncology Group Study. Cancer, 55, 1093-1098.
http://dx.doi.org/10.1002/1097-0142(19850301)55:5<1093::AID-CNCR2820550526>3.0.CO;2-O
has been cited by the following article:
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TITLE:
Retiform Sertoli-Leydig Cell Tumor of the Ovary
AUTHORS:
Gyu-Bong Yu, Seung-Kyu Choi, Yun-Dan Kang, Choong-Hak Park
KEYWORDS:
Sertoli-Leydig Cell Tumor, Retiform Pattern, Sex Cord-Stromal Tumor, Ovary
JOURNAL NAME:
International Journal of Clinical Medicine,
Vol.7 No.9,
September
13,
2016
ABSTRACT: Sertoli-Leydig cell tumor of the ovary is a kind of sex cord-stromal tumor, which occurs between teens and twenties with symptoms including abdominal pain and swelling. The incidence rate is infinitely rare comprising less than 0.5% of all ovarian tumor. The average age of “retiform Sertoli-Leydig cell tumor” is 17 years as compared to 25 years for Sertoli-Leydig cell tumors as a group. We have experienced this rare case of retiform Sertoli-Leydig cell tumor in a 25-year-old foreign patient with the complaint of palpable mass on the right lower quadrant and an irregular menstrual period. The patient underwent right salpingo-oophorectomy and tumor stage was FIGO stage 1A. We report with a brief review of literature.