Ovarian Steroid Cell Tumor (Not Otherwise Specified): A Case Report of Ovarian Hyperandrogenism

Author:

Faten Hadjkacem1,Dorra Ghorbel1ORCID,Slim Charfi2,Wajdi Safi1,Nadia Charfi1,Kais Chaabene3,Tahia Boudawara2,Mohamed Abid1

Affiliation:

1. Endocrinology Department, Hedi Chaker Hospital, 3029 Sfax, Tunisia

2. Department of Anatomical Pathology and Cytology, Habib Bourguiba Hospital, Sfax, Tunisia

3. Department of Gynecology, Hedi Chaker Hospital, 3029 Sfax, Tunisia

Abstract

Steroid cell tumors (SCTs) (not otherwise specified (NOS)) are rare sex cord-stromal tumors of the ovary. These are associated with hormonal disturbances resulting in menstrual bleeding patterns and androgenic effects. We report the case of a 36-year-old female presented with hirsutism, signs of virilization, and elevated androgen levels. Transvaginal ultrasound showed a solid-appearing right ovarian mass. She underwent fertility-sparing surgery with a laparoscopic left oophorectomy. Histological examination showed a benign steroid cell tumor, NOS. These tumors often small can then present a problem of positive diagnosis responsible for a delay in the diagnosis.

Publisher

Hindawi Limited

Subject

Oncology

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