约伯氏综合征伴川崎病家族史:一例报告及文献复习

Tamar Yared, Samer Mohsen
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引用次数: 1

摘要

背景:Job’s综合征或高免疫球蛋白E (IgE)综合征(HIES)是一种极为罕见的原发性免疫缺陷疾病,年发病率约小于百万分之一。它的特点是反复的感冒葡萄球菌感染,不寻常的湿疹性皮炎,严重的肺部感染和血清抗体IgE的广泛高浓度。病例介绍:本研究报告1例典型的有川崎病家族史的Job’s syndrome病例,旨在明确其临床特征、研究程序和治疗策略,评估耳鼻喉专科医师的作用,并强调Job’s syndrome与川崎病的可能关系。结论:一般情况下,早期发现和适当的护理可以预防工作综合征的发展。此外,在感染的最初迹象开始治疗是强制性的,以防止长期并发症。约伯和川崎之间可能存在一种关系,这需要更多的考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Job’s Syndrome With a Family History of Kawasaki Disease: A Case Presentation and Review of Literature
Background: Job’s syndrome or hyper-immunoglobulin E (IgE) syndrome (HIES) is an extremely rare primary immunodeficiency disease with an approximate annual incidence of less than 1/1000000. It is characterized by recurrent cold staphylococcal infections, unusual eczematous dermatitis, severe lung infections, and extensively high concentrations of the serum antibody IgE. Case Presentation: A typical case of Job’s syndrome with a family history of Kawasaki disease is presented in this study aiming at identifying the clinical features, investigational procedures, and management strategy, as well as evaluating the role of the ear, nose, and throat specialist and highlighting the probable relation between Job’s syndrome and Kawasaki disease. Conclusions: In general, early detection with proper care can prevent the progression of Job syndrome. In addition, the initiated treatment at the first signs of infection is mandatory for preventing long-term complications. There is a probable relation between Job and Kawasaki which requires more consideration.
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