| Literature DB >> 17961029 |
Dennis A Velez1, Marc R Mayberg, William H Ludlam.
Abstract
Endogenous Cushing syndrome (CS) results from hypercortisolemia caused by excess adrenocorticotropic hormone production in a pituitary adenoma or ectopic tumor, or by an adrenal tumor that directly produces excess cortisol. The diagnosis can usually be ascertained with a reasonable degree of certainty based on clinical and laboratory findings of hypercortisolism. There are patients, however, in whom the production of excess cortisol exhibits a cyclic or intermittent pattern, and, as a result, the clinical symptoms may be quite complex and varied. In these patients the hypothalamic-pituitary-adrenal axis may be normal between cycles, and dexamethasone suppression testing may produce a paradoxical response. In the present article, the authors provide a definition of cyclic Cushing syndrome, review the causes and its potential pathophysiological mechanisms, and discuss the treatment options based on a review of the available literature.Entities:
Mesh:
Substances:
Year: 2007 PMID: 17961029 DOI: 10.3171/foc.2007.23.3.5
Source DB: PubMed Journal: Neurosurg Focus ISSN: 1092-0684 Impact factor: 4.047