PDF(Pubmed)
Abstract：
Sertoli-Leydig cell tumor (SLCT) is a rare tumor of the ovary.Cushing\'s syndrome (CS), on the other hand, is a clinical picture formed by the long-term high levels of glucocorticoids in the blood for any reason and the resulting symptoms. Exceptionally in some of cases, a tumor far from the adrenal region synthesizes adrenocortical hormones. Among such ectopic neoplasms, CS Tumors of the ovary that secrete cortisol as a cause of the disease is an exceptional case. In other words, in this case, we argue that the tumor in the ovary causes Cushing\'s syndrome by secreting cortisol and ACTH-like peptides. There are 5 cases reported in the literature. In this case report we present a case in which SCLT of the ovary was detected by histopathological examination in a patient who underwent laparoscopic surgery due to Cushing\'s syndrome and bilateral adnexal mass.
摘要：
Sertoli-Leydig细胞瘤（SLCT）是一种罕见的卵巢肿瘤。库欣综合征（CS），另一方面,是由于任何原因血液中长期高水平的糖皮质激素以及由此产生的症状而形成的临床表现。在某些情况下，远离肾上腺区域的肿瘤合成肾上腺皮质激素。在这些异位肿瘤中，CS分泌皮质醇作为疾病原因的卵巢肿瘤是例外情况。换句话说,在这种情况下,我们认为卵巢肿瘤通过分泌皮质醇和ACTH样肽引起库欣综合征。文献报道5例。在此病例报告中，我们介绍了一例病例，其中由于库欣综合征和双侧附件肿块而接受腹腔镜手术的患者通过组织病理学检查发现了卵巢的SCLT。
