Chun Yoon Jung, Choi Hyun Jung, Lee Han Na, Cho Sook, Choi Ji Hyang
Department of Obstetrics and Gynecology, Seoul Medical Center, Seoul, Korea.
Obstet Gynecol Sci. 2013 Jan;56(1):50-5. doi: 10.5468/OGS.2013.56.1.50. Epub 2013 Jan 9.
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.
卵巢类固醇细胞瘤极为罕见,仅占所有卵巢肿瘤的0.1%。其中,未另行规定的(NOS)类固醇细胞瘤约占所有类固醇细胞瘤的56%。大多数类固醇细胞瘤分泌类固醇激素,只有约10%至15%的患者无症状。据报道,NOS类固醇细胞瘤的形态主要为实性,回顾1979年至今的病例报告,仅发现5例主要为囊性肿瘤的病例。本文报告了一例曾接受子宫切除术及腹膜包涵囊肿手术的患者,因其罕见性及不寻常的表现,并对文献进行简要回顾。该肿瘤未表现出类固醇激素分泌肿瘤的典型临床体征和症状,且形态不典型,主要为多房囊性,伴有少量实性部分。