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自身免疫性多腺体综合征II型:一例报告

Autoimmune Polyglandular Syndrome II: A Case Report.

作者信息

Awad Olfat, Basma Hadil, Masri Rim, Hamadeh Samih, Hamadeh Majdi

机构信息

Department of Nephrology, Lebanese University Faculty of Medical Sciences, Beirut, LBN.

Department of Endocrinology, Lebanese University Faculty of Medical Sciences, Beirut, LBN.

出版信息

Cureus. 2024 Jan 16;16(1):e52372. doi: 10.7759/cureus.52372. eCollection 2024 Jan.

Abstract

Autoimmune polyglandular syndrome II (APS-II), also known as Schmidt syndrome, is a rare endocrine disorder characterized by endocrine and non-endocrine illnesses. Addison's disease and at least one additional autoimmune condition, such as autoimmune thyroid disease or type 1 diabetes mellitus (T1DM), are features of APS-II. It can result from genetic and non-genetic factors. We present a case of a 60-year-old female patient with a history of T1DM and a recent diagnosis of Hashimoto's thyroiditis who was admitted to the nephrology department for hyponatremia. Investigations showed the presence of adrenal insufficiency (AI), so she was diagnosed with APS-II and had the full triad of this syndrome. Thus, it is important to think about the diagnosis of AI or other autoimmune conditions in a patient who already has one or more autoimmune diseases.

摘要

自身免疫性多腺体综合征II型(APS-II),也称为施密特综合征,是一种罕见的内分泌疾病,其特征为内分泌和非内分泌疾病。艾迪生病以及至少一种其他自身免疫性疾病,如自身免疫性甲状腺疾病或1型糖尿病(T1DM),是APS-II的特征。它可能由遗传和非遗传因素引起。我们报告一例60岁女性患者,有T1DM病史,近期诊断为桥本甲状腺炎,因低钠血症入住肾内科。检查显示存在肾上腺功能不全(AI),因此她被诊断为APS-II,并具备该综合征的全部三联征。因此,对于已经患有一种或多种自身免疫性疾病的患者,考虑诊断AI或其他自身免疫性疾病很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1657/10868629/b28c64e29938/cureus-0016-00000052372-i01.jpg

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