医学
肾
病变
肾肿块
促肾上腺皮质激素
神经内分泌肿瘤
放射科
左肾静脉
肾肿瘤
病理
内科学
激素
内分泌学
下腔静脉
肾切除术
作者
Si Xu,Yang Liu,Jinxin Zhou,Yifan Zhang
标识
DOI:10.1097/rlu.0000000000004595
摘要
Adrenocorticotropic hormone (ACTH)-secreting renal neuroendocrine tumor (NET) is extremely rare. A left renal mass was detected on ultrasound in a 26-year-old patient with ACTH-dependent Cushing syndrome. The lesion demonstrated slightly high density and moderate uptake of radiotracer on 68 Ga-DOTATATE PET/CT, suspected to be a NET. Renal vein sampling revealed excessive ACTH secretion from the left kidney. Histopathological examination after surgery finally confirmed the diagnosis of a functioning renal NET.
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