自身免疫性多内分泌腺综合征II型——病例报告

Autoimmune polyglandular syndrome type II - a case report.

作者信息

Azad A K, Islam M S, Quayum S L

机构信息

Dr Md Abul Kalam Azad, Associate Professor, Department of Medicine, Bangabandhu Sheikh Mujib Medical University, Shahbagh, Dhaka, Bangladesh.

出版信息

Mymensingh Med J. 2015 Jan;24(1):199-201.

PMID:25725692

Abstract

Autoimmune polyglandular syndrome also known as autoimmune polyendocrine syndrome (APS) type II is characterized by the presence of Addison's disease, in association with autoimmune thyroid disease and/or type I diabetes mellitus. Here a 14 year old girl is reported with Addison's disease, autoimmune hypothyroidism and primary hypogonadism. Autoimmune polyendocrine syndrome (APS) type II occurs most often in middle aged female and is quite rare in children but one should think to autoimmune polyglandular syndrome type II in patient at any age especially in patients with Addison's disease.

摘要

自身免疫性多腺体综合征也称为II型自身免疫性多内分泌综合征（APS），其特征是存在艾迪生病，并伴有自身免疫性甲状腺疾病和/或I型糖尿病。本文报道了一名14岁女孩患有艾迪生病、自身免疫性甲状腺功能减退症和原发性性腺功能减退症。II型自身免疫性多内分泌综合征（APS）最常发生于中年女性，在儿童中相当罕见，但对于任何年龄段的患者，尤其是患有艾迪生病的患者，都应考虑II型自身免疫性多腺体综合征。