原发性免疫缺陷可能被误诊为牛奶过敏:7例转至三级儿科医院。

ISRN pediatrics Pub Date : 2013-09-30 eCollection Date: 2013-01-01 DOI:10.1155/2013/470286
Karina Mescouto Melo, Ellen Dantas, Maria Isabel De Moraes-Pinto, Antonio Condino-Neto, Isabela G S Gonzalez, Marcia C Mallozi, Jackeline M Franco, Beatriz T Costa-Carvalho
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引用次数: 14

摘要

介绍。在牛奶过敏(CMA)和一些原发性免疫缺陷疾病(PID)中经常观察到湿疹和胃肠道症状的存在。目标。本研究描述了7例经三级过敏/免疫学中心诊断为CMA,最终诊断为PID的患者。方法。这是一项基于医疗记录的临床和实验室数据的回顾性研究。结果。7名年龄在3个月至6岁之间的患者(6名男性)被推荐诊断为CMA。他们表现为湿疹和/或胃肠道症状。其中5人接受了替换配方奶粉。所有患者均表现出其他临床特征,包括与CMA无关的严重/复发性感染,其中2例有PID阳性家族史。实验室检查显示所有患者免疫系统功能紊乱。这些儿童被诊断为高ige和Wiskott-Aldrich综合征、CD40L缺乏症、严重联合免疫缺陷症、x连锁无球蛋白血症、婴儿短暂性低γ球蛋白血症和慢性肉芽肿病。总之,过敏性疾病和免疫缺陷是免疫系统异常的不同频谱的结果,可能被误诊。在临床医生和儿科医生中开展PID教育项目可以减少这种误诊的发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary Immunodeficiency May Be Misdiagnosed as Cow's Milk Allergy: Seven Cases Referred to a Tertiary Pediatric Hospital.

Introduction. The presence of eczema and gastrointestinal manifestations are often observed in cow's milk allergy (CMA) and also in some primary immunodeficiency diseases (PID). Objective. To describe 7 patients referred to a tertiary allergy/immunology Center with a proposed diagnosis of CMA, who were ultimately diagnosed with PID. Methods. This was a retrospective study based on clinical and laboratory data from medical records. Results. Seven patients (6 males) aged between 3 mo and 6 y were referred to our clinic with a proposed diagnosis of CMA. They presented with eczema and/or gastrointestinal symptoms. Five were receiving replacement formula. All patients presented with other clinical features, including severe/recurrent infections unrelated to CMA, and two of them had a positive family history of PID. Laboratory tests showed immune system dysfunctions in all patients. Hyper-IgE and Wiskott-Aldrich syndromes, CD40L deficiency, severe combined immunodeficiency, X-linked agammaglobulinemia, transient hypogammaglobulinemia of infancy, and chronic granulomatous disease were diagnosed in these children. In conclusion, allergic diseases and immunodeficiency are a result of a different spectrum of abnormalities in the immune system and may be misdiagnosed. Educational programs on PID among clinical physicians and pediatricians can reduce the occurrence of this misdiagnosis.

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