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2型自身免疫性多腺体综合征:一种不寻常的表现。

Autoimmune polyglandular syndrome type 2: an unusual presentation.

作者信息

Karamifar Hamdollah, Dalili Satila, Karamizadeh Zohreh, Amirhakimi Gholamhosein, Dalili Hosein

机构信息

Department of Pediatric Endocrinology and Metabolism, School of Medicine, Shiraz University of Medical Sciences, Fars, Iran.

出版信息

Acta Med Iran. 2010 May-Jun;48(3):196-7.

Abstract

Autoimmune polyglandular syndrome (APS) type 2 is characterized by the presence of Addison's disease, in association with autoimmune thyroid disease and/or type 1 diabetes mellitus. APS type 2 occurs most often in middle aged females and is rare in children. Here an 11 year old boy is reported with Addison's disease who developed symptom's of diabetes mellitus, goiter, malabsorption, macrocytic anemia and keratitis. APS type 2 occurs most often in middle aged females and is quite rare in children but one should think to autoimmune poly glandular syndrome type II in patient at any age especially in patients with Addison's disease.

摘要

2型自身免疫性多腺体综合征(APS)的特征是存在艾迪生病,并伴有自身免疫性甲状腺疾病和/或1型糖尿病。2型APS最常发生于中年女性,在儿童中罕见。本文报告了一名11岁患有艾迪生病的男孩,他出现了糖尿病、甲状腺肿、吸收不良、大细胞性贫血和角膜炎的症状。2型APS最常发生于中年女性,在儿童中相当罕见,但对于任何年龄的患者,尤其是患有艾迪生病的患者,都应考虑到II型自身免疫性多腺体综合征。

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