Velez Dennis A, Mayberg Marc R, Ludlam William H
Seattle Neuroendocrine Program, Swedish Neuroscience Institute, Seattle, Washington, USA.
Neurosurg Focus. 2007;23(3):E4; discussion E4a. doi: 10.3171/foc.2007.23.3.5.
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.
内源性库欣综合征(CS)是由垂体腺瘤或异位肿瘤中促肾上腺皮质激素分泌过多,或肾上腺肿瘤直接分泌过多皮质醇导致高皮质醇血症引起的。通常根据高皮质醇血症的临床和实验室检查结果,能够以合理的确定性做出诊断。然而,有些患者的皮质醇分泌呈现周期性或间歇性模式,因此临床症状可能非常复杂多样。在这些患者中,下丘脑 - 垂体 - 肾上腺轴在周期之间可能是正常的,地塞米松抑制试验可能会产生矛盾反应。在本文中,作者给出了周期性库欣综合征的定义,回顾了其病因及其潜在的病理生理机制,并基于对现有文献的综述讨论了治疗方案。