Symptomatic Ovarian Steroid Cell Tumor not Otherwise Specified in a Post-Menopausal Woman
Author(s) -
Neha Sood,
Kaniksha Desai,
Ana-Maria Chindris,
Jason Lewis,
Tri A. Dinh
Publication year - 2016
Publication title -
rare tumors
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.285
H-Index - 15
eISSN - 2036-3613
pISSN - 2036-3605
DOI - 10.4081/rt.2016.6200
Subject(s) - virilization , medicine , testosterone (patch) , ovary , occult , ovarian tumor , leydig cell tumor , gynecology , hormone , pathology , androgen , ovarian cancer , luteinizing hormone , cancer , leydig cell , alternative medicine
Steroid cell tumor not otherwise specified (NOS) is a rare subtype of sex cord stromal tumor of the ovary and contributes less than 0.1% of all ovarian neoplasms. The majority of tumors occur in pre-menopausal women (mean age: 43 years), in which 56-77% of patients present with virilization due to excess testosterone. An 80-year-old woman with worsening alopecia and excessive growth of coarse hair on abdomen and genital area was found to have elevated serum testosterone level (462 ng/mL). Radiologic studies were consistent with bilateral adrenal adenomas. Bilateral adrenal venous sampling ruled out the adrenal gland as origin of hormone secretion. A diagnostic and therapeutic bilateral salpingooophorectomy confirmed steroid cell tumor NOS of the left ovary. Post-operatively, the patient had complete resolution of her symptoms and normalization of testosterone level. Our case emphasizes the importance of a clinical suspicion for an occult testosterone secreting ovarian tumor in a symptomatic patient without obvious ovarian mass on imaging
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