卵巢间质黄体瘤一例报告并文献复习

Stromal Luteoma of The Ovary: A Case Report and Literature Review

卵巢类固醇细胞瘤是一种少见的卵巢肿瘤,约占卵巢肿瘤≤0.1%,根据其肿瘤组织的来源分为间质黄体瘤、Leydig细胞瘤、非特异性类固醇细胞瘤3类。卵巢间质黄体瘤是临床少见疾病,其无特异性表现,彩色超声和影像学检查不易查出,容易造成术前误诊、漏诊。本文回顾性分析我院收治的卵巢间质黄体瘤临床资料并进行相关文献复习,卵巢间质黄体瘤的确诊需结合临床表现及术后病理,手术是其主要治疗方法。

Steroid cell tumors account for less than 0.1% of all ovarian tumors. There are three steroid cell tumor subtypes: stromal luteoma, Leydig cell tumor and steroid cell tumor not otherwise specified (NOS). Stromal luteoma is a rare disease. The clinical manifestations of stromal luteoma are unspecific, so it is hard to diagnosis before operation. In this study, we report a case of 47-year-old female who suffers from stromal luteoma. And we review the literatures about the case reports systematically. And we found that the diagnosis of ovarian stromal luteoma is based on abnormal uterine bleeding and pathology, and surgery is the most important treatment method.