Addison's disease

Vincent Simpson, Antonia M Brooke
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引用次数: 0

Abstract

Addison's disease, or primary adrenocortical failure, is rare, most commonly caused in the UK by autoimmune destruction of the adrenal glands. The insidious onset of symptoms over many months means there is often a delay in diagnosis and patients can first present in adrenal crisis, which is life-threatening if not appropriately treated. The diagnosis is made by finding a low serum cortisol at 09:00 hours in the presence of an elevated adrenocorticotropic hormone (ACTH) concentration, or by a suboptimal cortisol response to exogenous ACTH on provocation testing. Replacement with hydrocortisone and fludrocortisone should approximate physiological concentrations as closely as possible. Patients and families should have a good understanding of the condition and how to adjust the corticosteroid dosing in times of illness.
阿狄森氏病
阿狄森氏病,或原发性肾上腺皮质衰竭,是罕见的,最常见的原因是在英国的自身免疫性破坏肾上腺。症状的潜伏发作会持续数月,这意味着诊断往往会延迟,患者可能首先表现为肾上腺危机,如果治疗不当,可能会危及生命。诊断是通过在09:00时发现促肾上腺皮质激素(ACTH)浓度升高的情况下血清皮质醇水平低,或在激发试验中发现皮质醇对外源性ACTH的反应不理想。用氢化可的松和氟化可的松替代应尽可能接近生理浓度。患者和家属应该很好地了解病情以及如何在患病时调整皮质类固醇的剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
1.10
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