Tissue regenerates of adrenal cortex with a physiological function twelve years after bilateral total adrenalectomy for Cushing's syndrome.

R Hampel, E Finger, W Meng
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引用次数: 3

Abstract

We report about a male patient, who underwent bilateral total adrenalectomy due to ACTH-dependent Cushing's syndrome without pituitary adenoma in his 11th year of life. Symptoms of Cushing's disease were absent during the follow-up period. Height and body weight followed the percentiles 25 and 50 respectively. An endogenous cortisol production was not detected and steroid substitution became necessary. Five years after the surgery, he showed normal cortisol levels, but there was no cortisol increase under ACTH-loading. Nine and 12 years (1993) after surgery, we found normal, physiological levels of cortisol suggestive of normal functioning adrenal glands (day profile of cortisol, Liddle-Test, ACTH-Test, CRH-Test, cortisol excretion in 24-h-urine). Moreover, baseline ACTH and its rise under CRH stimulation were normal. Scintigraphy revealed normal-sized adrenal tissue in orthotopic position on both sides. Steroid supplementation was discontinued. Presently the patient is healthy, active and under no steroid therapy. No evidence of residual or relapsing Cushing's disease or Nelson's syndrome has been found up to this point.

库欣综合征双侧肾上腺全切除术12年后具有生理功能的肾上腺皮质组织再生。
我们报告一位男性患者,在11岁时因acth依赖性库欣综合征(无垂体腺瘤)行双侧肾上腺全切除术。随访期间无库欣病症状。身高和体重的百分位数分别为25和50。内源性皮质醇的产生没有检测到,类固醇替代成为必要的。手术后5年,他的皮质醇水平正常,但在acth负荷下没有皮质醇升高。手术后9年和12年(1993年),我们发现正常的皮质醇生理水平提示肾上腺功能正常(皮质醇日谱,Liddle-Test, ACTH-Test, CRH-Test, 24小时尿液中的皮质醇排泄)。此外,基线ACTH及其在CRH刺激下的上升正常。闪烁显像显示正常大小的肾上腺组织在正位两侧。停止类固醇补充。目前患者健康、活跃,未接受类固醇治疗。到目前为止,还没有发现残留或复发的库欣氏病或纳尔逊氏综合征的证据。
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