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首页> 外文期刊>The Endocrinologist >Autoimmune Polyendocrine Syndrome Presenting As Diabetic Ketoacidosis in a 20-Year-Old Woman With Crohn Disease A Case Report
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Autoimmune Polyendocrine Syndrome Presenting As Diabetic Ketoacidosis in a 20-Year-Old Woman With Crohn Disease A Case Report

机译:自身免疫性多内分泌综合征,表现为糖尿病酮症酸中毒在一名20岁克罗恩病女性中的一例报道

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摘要

Autoimmune polyendocrine syndrome (APS) is defined as a multiple endocrine gland insufficiency associated with an autoimmune disease. The first clinical manifestation of APS-1 usually occurs in childhood and new components may successively appear throughout life, with the majority of patients (63%) have 3 to 5 organ involvement. The.most frequent manifestations of APS include chronic mucocutaneous candidiasis, hypopar-athyroidism, adrenocortical failure, and gonadal failure in females. We present a case of APS that cannot be classified in any group of APS presenting with Crohn disease.
机译:自身免疫性多内分泌综合征(APS)定义为与自身免疫性疾病相关的多发性内分泌腺体功能不全。 APS-1的首次临床表现通常发生在儿童时期,一生中可能会陆续出现新的成分,大多数患者(63%)有3至5个器官受累。 APS最常见的表现包括女性慢性粘膜皮肤念珠菌病,甲状旁腺功能低下,肾上腺皮质功能衰竭和性腺功能衰竭。我们提出一例不能归类为克罗恩病的APS病例。

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