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首页> 外文期刊>Allergy >Classification, diagnosis, and approach to treatment for angioedema: Consensus report from the Hereditary Angioedema International Working Group
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Classification, diagnosis, and approach to treatment for angioedema: Consensus report from the Hereditary Angioedema International Working Group

机译：血管性水肿的分类，诊断和治疗方法：遗传性血管性水肿国际工作组的共识报告

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Angioedema is defined as localized and self-limiting edema of the subcutaneous and submucosal tissue, due to a temporary increase in vascular permeability caused by the release of vasoactive mediator(s). When angioedema recurs without significant wheals, the patient should be diagnosed to have angioedema as a distinct disease. In the absence of accepted classification, different types of angioedema are not uniquely identified. For this reason, the European Academy of Allergy and Clinical Immunology gave its patronage to a consensus conference aimed at classifying angioedema. Four types of acquired and three types of hereditary angioedema were identified as separate forms from the analysis of the literature and were presented in detail at the meeting. Here, we summarize the analysis of the data and the resulting classification of angioedema.
机译：血管性水肿定义为皮下和粘膜下组织的局限性自限性水肿，这是由于血管活性介质释放引起的血管通透性暂时升高所致。当血管水肿复发而没有明显的风团时，应诊断出患者患有血管水肿是一种独特的疾病。在没有公认的分类的情况下，不能唯一地识别出不同类型的血管性水肿。因此，欧洲过敏与临床免疫学会赞助了一场旨在对血管性水肿进行分类的共识会议。从文献分析中确定了四种类型的获得性和三种类型的遗传性血管性水肿是分开的形式，并在会议上进行了详细介绍。在这里，我们总结了数据分析和血管水肿的分类结果。

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