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嗜酸性肉芽肿性多血管炎诊治规范多学科专家共识

2018-07-12 中国风湿免疫科相关专家小组（统称） 中华结核和呼吸杂志, 2018,41(7) : 514-521.

嗜酸性肉芽肿性多血管炎诊治规范

嗜酸性肉芽肿性多血管炎(eosinophilic granulomatosis with polyangiitis，EGPA)是一种可累及全身多个系统的、少见的自身免疫性疾病，主要表现为外周血及组织中嗜酸粒细胞增多、浸润及中小血管的坏死性肉芽肿性炎症，属于抗中性粒细胞胞质抗体(anti-neutrophil cytoplasmic antibodies，ANCA)相关性系统性血管炎。 EGPA可累

中文标题：

嗜酸性肉芽肿性多血管炎诊治规范多学科专家共识

发布机构：

中国风湿免疫科相关专家小组（统称）

发布日期：

2018-07-12

简要介绍：

嗜酸性肉芽肿性多血管炎(eosinophilic granulomatosis with polyangiitis，EGPA)是一种可累及全身多个系统的、少见的自身免疫性疾病，主要表现为外周血及组织中嗜酸粒细胞增多、浸润及中小血管的坏死性肉芽肿性炎症，属于抗中性粒细胞胞质抗体(anti-neutrophil cytoplasmic antibodies，ANCA)相关性系统性血管炎。 EGPA可累及多系统或器官，由于我国缺乏EGPA大样本的临床数据和资料，不同学科对该病的描述与诊治存在差异。为进一步提高我国各学科对该病的系统认识及临床诊疗水平，由广州呼吸健康研究院钟南山院士、陈荣昌院长及中山大学附属第三医院风湿科古洁若教授牵头，广泛征求国内外多学科专家的意见，同时参考国内外近年来EGPA的研究成果与诊治经验，制定了我国首个EGPA诊治规范多学科专家共识。

拓展指南：与血管炎相关指南：

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    2021-07-24 xianglala6

    学习

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    2021-04-22 ms7000001881586700

    棒棒哒

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    2021-04-09 ms8000001350439055

    厉害厉害厉害

    0

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    2018-08-11 xiaotao112411

    学习学习学习

    0

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    2018-08-11 xiaotao112411

    学习学习学习

    0

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