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Ovarian Leydig Cell Hyperplasia: An Unusual Case of Virilization in a Postmenopausal Woman
Author(s) -
Jaya Mehta,
Jeffrey L. Miller,
Anthony J. Can,
Stacey K. Mardekian,
Lawrence C. Kenyon,
Serge Jabbour
Publication year - 2014
Publication title -
case reports in endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.26
H-Index - 6
eISSN - 2090-6501
pISSN - 2090-651X
DOI - 10.1155/2014/762745
Subject(s) - virilization , medicine , hirsutism , testosterone (patch) , leydig cell tumor , past medical history , medical history , gynecology , hyperandrogenism , hyperplasia , hysterectomy , leydig cell , endocrinology , hormone , diabetes mellitus , androgen , surgery , polycystic ovary , luteinizing hormone , insulin resistance
Objective . To report an unusual case of ovarian Leydig cell hyperplasia resulting in virilization in a postmenopausal woman. Methods . Patient's medical history and pertinent literature were reviewed. Results . A 64-year-old woman presented with virilization with worsening hirsutism, deepening of her voice, male musculature, and male pattern alopecia. Her pertinent past medical history included type 1 diabetes, hyperlipidemia, and hypertension. Her pertinent past surgical history included hysterectomy due to fibroids. On further work-up, her serum total testosterone was 506 ng/dL (nl range: 2–45) and free testosterone was 40 pg/mL (nl range: 0.1–6.4). After ruling out adrenal causes, the patient underwent an empiric bilateral oophorectomy that showed Leydig cell hyperplasia on pathology. Six weeks postoperatively, serum testosterone was undetectable with significant clinical improvement. Conclusion . Postmenopausal hyperandrogenism can be the result of numerous etiologies ranging from normal physiologic changes to ovarian or rarely adrenal tumors. Our patient was found to have Leydig cell hyperplasia of her ovaries, a rarely reported cause of virilization.

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