Hao Zhixin, Ding Jie, Huo Li, Luo Yaping
Department of Nuclear Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College Hospital, Beijing 100730, China.
Beijing Key Laboratory of Molecular Targeted Diagnosis and Therapy in Nuclear Medicine, Beijing 100730, China.
Diagnostics (Basel). 2022 Aug 11;12(8):1937. doi: 10.3390/diagnostics12081937.
We report a rare case of Cushing's syndrome induced by an ectopic adrenocortical adenoma. A 57-year-old woman was diagnosed with adrenocorticotropic hormone (ACTH)-independent Cushing's syndrome based on clinical manifestation and laboratory information. She was found to have a mass in the left renal hilum via contrast-enhanced computed tomography (CT). The mass was negative, as seen in somatostatin receptor imaging with Tc-hydrazinonicotinyl-Tyr3-octreotide (HYNIC-TOC), and showed mild fluorodeoxyglucose (FDG) activity via positron emission tomography (PET)/CT. The results of adrenal venous sampling suggested a left-side adrenal origin of hypercortisolism, possibly secreted by the mass in the renal hilum. Histopathology after surgical resection of the mass confirmed an ectopic adrenocortical adenoma, which was responsible for the patient's Cushing's syndrome. During the 8-month follow-up after surgery, no recurrence of Cushing's syndrome was found.
我们报告一例由异位肾上腺皮质腺瘤引起的库欣综合征罕见病例。一名57岁女性根据临床表现和实验室检查结果被诊断为促肾上腺皮质激素(ACTH)非依赖性库欣综合征。通过增强计算机断层扫描(CT)发现她左肾门处有一个肿块。在使用锝-肼基烟酰基-Tyr3-奥曲肽(HYNIC-TOC)进行的生长抑素受体显像中,该肿块呈阴性,并且通过正电子发射断层扫描(PET)/CT显示有轻度氟脱氧葡萄糖(FDG)活性。肾上腺静脉采血结果提示高皮质醇血症起源于左侧肾上腺,可能由肾门处的肿块分泌。肿块手术切除后的组织病理学检查证实为异位肾上腺皮质腺瘤,该腺瘤导致了患者的库欣综合征。术后8个月的随访期间,未发现库欣综合征复发。