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伴有自发缓解的间歇性库欣病

Intermittent Cushing's disease with spontaneous remission.

作者信息

Scott R S, Espiner E A, Donald R A

出版信息

Clin Endocrinol (Oxf). 1979 Nov;11(5):561-6. doi: 10.1111/j.1365-2265.1979.tb03109.x.

Abstract

A patient with well documented Cushing's syndrome, associated with excessive secretion of ACTH, was studied over a 20 month period. During this time there were three episodes of spontaneous biochemical remission and except for a 7 day period of exacerbation the patient has had normal cortisol production for the last 15 months. During this recent prolonged remission period, repeat pituitary function testing demonstrated persistent abnormalities of the hypothalamic pituitary axis, in that ACTH failed to respond to a hypoglycaemic stimulus. However in all other respects adrenal function was normal with preservation of diurnal rhythmicity of cortisol and ACTH, and intact dexamethasone suppressability of cortisol. The additional unusual features of normal GH and TSH responses to stimulation, during either remission or exacerbation, suggest a subtle and localized hypothalamic defect in this case.

摘要

对一名记录完备的库欣综合征患者进行了为期20个月的研究,该患者伴有促肾上腺皮质激素(ACTH)分泌过多。在此期间,出现了三次自发性生化缓解,除了一次为期7天的病情加重期外,患者在过去15个月里皮质醇分泌正常。在最近这次长期缓解期,重复进行的垂体功能测试显示下丘脑 - 垂体轴持续存在异常,即ACTH对低血糖刺激无反应。然而,在所有其他方面,肾上腺功能正常,皮质醇和ACTH的昼夜节律得以保留,且皮质醇对地塞米松具有正常的抑制反应。在缓解期或病情加重期,生长激素(GH)和促甲状腺激素(TSH)对刺激的反应正常,这一额外的不寻常特征表明该病例存在细微的局限性下丘脑缺陷。

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