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皮肤色素沉着与Ⅱ型多腺体自身免疫综合征

Cutaneous hyperpigmentation and polyglandular autoimmune syndrome type II.

作者信息

Chung A D, English J C

机构信息

Department of Medicine, Darnall Army Community Hospital, Fort Hood, Texas, USA.

出版信息

Cutis. 1997 Feb;59(2):77-80.

PMID:9040976
Abstract

Primary adrenal insufficiency (Addison's disease) may initially present with cutaneous hyperpigmentation. Addison's disease, when associated with autoimmune thyroid disease and/or insulin-dependent diabetes mellitus, is referred to as polyglandular autoimmune syndrome type II. We present the case of a patient who initially was diagnosed as having Grave's disease and eventually Addison's disease due to persistent cutaneous hyperpigmentation, fatigue, weight loss, hypotension, hyponatremia, peripheral eosinophilia, and positive results of a synthetic corticotropin stimulation test. Addison's disease, polyglandular autoimmune syndrome type II, and cutaneous hyperpigmentation are reviewed.

摘要

原发性肾上腺皮质功能减退症(艾迪生病)最初可能表现为皮肤色素沉着。艾迪生病若与自身免疫性甲状腺疾病和/或胰岛素依赖型糖尿病相关,则被称为Ⅱ型多腺体自身免疫综合征。我们报告一例患者,该患者最初被诊断为格雷夫斯病,最终因持续的皮肤色素沉着、疲劳、体重减轻、低血压、低钠血症、外周嗜酸性粒细胞增多以及促肾上腺皮质激素合成刺激试验结果呈阳性而被诊断为艾迪生病。本文对艾迪生病、Ⅱ型多腺体自身免疫综合征及皮肤色素沉着进行了综述。

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