| Literature DB >> 27695589 |
Fan Chen1, Xiangyu Wang2, Yang Wang3, Hui Meng4, Xinguo Hou5, Yaofeng Zhu4, Wei Gao6, Xuewen Jiang4, Shouzhen Chen4, Zhaocun Zhang4, Zhichuan Zou4, Tianyi He5, Yue Yang4, Kejia Zhu4, Yong Wang4, Yaxiao Liu4, Jianfeng Cui4, Benkang Shi4, Gang Yin4.
Abstract
Extra-adrenal pheochromocytomas, or paragangliomas, are rare tumours that derive from extra-adrenal chromaffin cells. Cushing's syndrome (CS) caused by paragangliomas is extremely rare. We report a 53-year-old man with hypertension, diabetes, and symptoms of hypokalemia. Computer tomography (CT) revealed two retroperitoneal masses and bilateral adrenal hyperplasia. Together with the laboratory examinations, ectopic CS caused by multiple paragangliomas was highly suspected. The patient underwent resections of retroperitoneal tumours, left kidney, and left adrenal; postoperative histopathology confirmed two paragangliomas that were both positively stained for adrenocorticotropic hormone (ACTH). He got clinical and biochemical recoveries without any recurrent evidence at the nine-month followup.Entities:
Year: 2016 PMID: 27695589 PMCID: PMC5028219 DOI: 10.5489/cuaj.3153
Source DB: PubMed Journal: Can Urol Assoc J ISSN: 1911-6470 Impact factor: 1.862