Rare Tumors (Jun 2016)

Symptomatic ovarian steroid cell tumor not otherwise specified in a post-menopausal woman

  • Neha Sood,
  • Kaniksha Desai,
  • Ana-Maria Chindris,
  • Jason Lewis,
  • Tri A. Dinh

DOI
https://doi.org/10.4081/rt.2016.6200
Journal volume & issue
Vol. 8, no. 2

Abstract

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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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