Endocrinology and Metabolism Institute, Cleveland Clinic, Cleveland, Ohio 44195, USA.
J Surg Oncol. 2012 Oct 1;106(5):565-71. doi: 10.1002/jso.23197. Epub 2012 Jun 27.
Cushing's syndrome (CS) results from prolonged exposure to elevated endogenous cortisol. Majority of cases are caused by ACTH, pituitary, or ectopic origin. Primary adrenal hypersecretion is 15-20% caused by adenomas, carcinomas (ACC), and rarely by nodular adrenocortical disease. CS presents with all typical features. Commonly recommended initial testing are urinary free cortisol, late-night salivary cortisol, and 1-mg overnight dexamethasone suppression test (DST). Imaging is the key to diagnosis. CS continues to pose diagnostic and therapeutic challenges; life-long follow-up is mandatory.
库欣综合征(CS)是由于长期暴露于内源性皮质醇升高所致。大多数病例由 ACTH、垂体或异位起源引起。原发性肾上腺过度分泌是由腺瘤、癌(ACC)引起的,占 15-20%,很少由结节性肾上腺皮质疾病引起。CS 具有所有典型特征。通常建议进行初始检测的是尿游离皮质醇、夜间唾液皮质醇和 1mg 过夜地塞米松抑制试验(DST)。影像学检查是诊断的关键。CS 仍然存在诊断和治疗方面的挑战;必须进行终身随访。