Watanobe H, Nigawara T, Nasushita R, Sasaki S, Takebe K
Third Department of Internal Medicine, Hirosaki University School of Medicine, Aomori, Japan.
Eur J Endocrinol. 1995 Sep;133(3):317-9. doi: 10.1530/eje.0.1330317.
We experienced an extremely unusual combination of Cushing's disease and corticosteroid-binding globulin (CBG) deficiency that has been reported in only one similar case to date. A 53-year-old woman presented at a medical clinic with clinical Cushing's disease. However, her plasma levels of adrenocorticotropin (ACTH) and cortisol were in the normal range. Six months later, during a second visit, a high urinary excretion of 17-hydroxycorticosteroids was found, but plasma ACTH and cortisol levels were normal again. Further investigation revealed a decreased CBG concentration. Free plasma cortisol levels were clearly elevated. Furthermore, the Cushing's disease of our patient was complicated by periodic secretion of ACTH and cortisol, with high or normal outputs of corticosteroids occurring alternately every 1-3 days, which explained the occasionally normal plasma ACTH and cortisol levels. A combination of a decreased serum CBG concentration and periodic secretion of ACTH can be an important pitfall in the diagnosis of Cushing's disease.
我们遇到了库欣病与皮质类固醇结合球蛋白(CBG)缺乏这一极为罕见的组合,迄今为止仅有一例类似病例报道。一名53岁女性因临床库欣病就诊于一家诊所。然而,她的血浆促肾上腺皮质激素(ACTH)和皮质醇水平在正常范围内。六个月后,第二次就诊时发现尿17-羟皮质类固醇排泄量很高,但血浆ACTH和皮质醇水平再次正常。进一步检查发现CBG浓度降低。游离血浆皮质醇水平明显升高。此外,我们患者的库欣病伴有ACTH和皮质醇的周期性分泌,皮质类固醇的高分泌或正常分泌每1 - 3天交替出现一次,这解释了血浆ACTH和皮质醇水平偶尔正常的原因。血清CBG浓度降低与ACTH周期性分泌相结合可能是库欣病诊断中的一个重要陷阱。