Izumi T, Sasagawa I, Suzuki H, Kubota Y, Nakada T, Nishikawa T
Department of Urology, Yamagata University School of Medicine, Japan.
Urol Int. 1997;58(4):262-5. doi: 10.1159/000283000.
We report a man with pre-Cushing's syndrome due to ACTH-independent bilateral macronodular adrenocortical hyperplasia. Plasma ACTH was low and urinary 17-OHCS was not suppressed by a high dose of dexamethasone (8 mg), but plasma cortisol was responsive to exogenous ACTH. The adrenal glands were enlarged and contained multiple nodules composed of large clear cells and small compact cells. The steroid levels in the adrenal glands were lower than those in overt Cushing's syndrome due to the adrenocortical adenoma. This suggests that the tumor produces insufficient amounts of active hormones to have a clinical effect.
我们报告一例因促肾上腺皮质激素(ACTH)非依赖性双侧大结节性肾上腺皮质增生导致的库欣综合征前期男性患者。血浆ACTH水平较低,高剂量地塞米松(8毫克)未能抑制尿17-羟皮质类固醇(17-OHCS),但血浆皮质醇对外源性ACTH有反应。肾上腺增大,含有多个由大透明细胞和小致密细胞组成的结节。与肾上腺皮质腺瘤导致的显性库欣综合征相比,该患者肾上腺中的类固醇水平较低。这表明肿瘤产生的活性激素量不足以产生临床效应。