| Literature DB >> 22740318 |
Abstract
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.Entities:
Mesh:
Year: 2012 PMID: 22740318 DOI: 10.1002/jso.23197
Source DB: PubMed Journal: J Surg Oncol ISSN: 0022-4790 Impact factor: 3.454