- Author:
Yoon Jung CHUN
1
;
Hyun Jung CHOI
;
Han Na LEE
;
Sook CHO
;
Ji Hyang CHOI
Author Information
- Publication Type:Case Report
- Keywords: Steroid cell tumor; Ovary; Cystic
- MeSH: Accounting; Female; Humans; Hysterectomy; Ovary
- From:Obstetrics & Gynecology Science 2013;56(1):50-55
- CountryRepublic of Korea
- Language:English
- Abstract: Steroid cell tumors of the ovary are extremely rare, accounting for only 0.1% of all ovarian tumors. Of these, steroid cell tumors, not otherwise specified (NOS) constitute about 56% of all steroid cell tumors. Most steroid cell tumors secrete steroid hormones, and only about 10% to 15% of patients are asymptomatic. The morphology of steroid cell tumors, NOS is predominantly reported to be solid, and a review of case reports from 1979 until now revealed only 5 cases that were mainly cystic tumors. The present case, in a patient who had undergone a previous hysterectomy and surgery for a peritoneal inclusion cyst, is reported due to its rarity and its unusual presentation, together with a brief review of the literature. The tumor showed no clinical signs and symptoms typical of a steroid hormone secreting tumor and had an atypical morphology, being primarily multi-septate cystic with a minor solid portion.