Rjoop Anwar, Almohtaseb Alia, Al Aruri Daoud O, Hyari Dina, Shugaer Mohammad Abu
Department of Pathology and Microbiology, Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan.
Pathology department, King Abdullah University Hospital, Jordan university of science and technology, Irbid, Jordan.
Future Sci OA. 2024 Dec 31;10(1):2424144. doi: 10.1080/20565623.2024.2424144. Epub 2024 Nov 21.
Leydig cell tumors (LCT) are rare neoplasms that represent less than 0.1% of all ovarian tumors. This tumor usually presents with signs and symptoms of excess androgen levels. Diagnosis is made based on a combination of history, laboratory findings, imaging techniques and histopathological findings. We present the case of a 35-year-old gravida five para 3 pregnant woman with a unilateral ovarian cystic mass that was discovered incidentally during a cesarean section. The cyst measured 9 cm in its maximum dimension. A left oophorectomy was performed after the delivery of an alive male baby. Morphological and immunophenotypic findings were consistent with those of a pure Leydig cell tumor. Leydig cell tumors are uncommon and usually present with hyperandrogenism. The presentation could be polymorphic, ranging from the rapid onset of virilization to being asymptomatic.
睾丸间质细胞瘤(LCT)是一种罕见的肿瘤,占所有卵巢肿瘤的比例不到0.1%。这种肿瘤通常表现为雄激素水平过高的体征和症状。诊断基于病史、实验室检查结果、影像学技术和组织病理学检查结果的综合判断。我们报告一例35岁、孕5产3的孕妇,在剖宫产术中偶然发现单侧卵巢囊性肿物。囊肿最大直径为9厘米。在分娩一名存活男婴后,进行了左侧卵巢切除术。形态学和免疫表型检查结果与纯睾丸间质细胞瘤一致。睾丸间质细胞瘤并不常见,通常表现为高雄激素血症。其表现可能多种多样,从迅速出现男性化到无症状。