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Churg-strauss syndrome: an update.

机译:楚格·史特劳斯综合征:更新。

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摘要

Churg-Strauss syndrome is an uncommon disease of unknown cause described initially by Churg and Strauss in 1951. Even though it was initially thought to be a variant of polyarteritis nodosa, its pathological, clinical, and laboratory features show that it is related to the small vessel vasculitides, and it is now classified as an antineutrophil cytoplasmic antibody-associated vasculitis. The presence of asthma, usually of adult onset, along with other allergic symptoms, peripheral and tissue eosinophilia, is specific to this disease. These features usually help clinicians distinguish it from other types of small vessel vasculitis and should alert clinicians about its presence. Two different clinical subtypes defined by the presence of antineutrophil cytoplasmic antibodies recently have been recognized. Recent advances in the treatment and pathophysiology of Churg-Strauss syndrome are reviewed in this article.
机译:Churg-Strauss综合征是一种罕见的原因不明的罕见疾病,最初由Churg和Strauss于1951年描述。尽管最初被认为是结节性多动脉炎的一种变体,但其病理,临床和实验室特征表明它与小结节有关。血管炎,现在被归类为抗中性粒细胞胞浆抗体相关的血管炎。通常是成人发作的哮喘以及其他过敏性症状,外周和组织嗜酸性粒细胞增多是该疾病的特异性症状。这些功能通常可以帮助临床医生将其与其他类型的小血管血管炎区分开来,并应提醒临床医生其存在。最近已经认识到由抗中性粒细胞胞浆抗体的存在定义的两种不同的临床亚型。本文综述了Churg-Strauss综合征的治疗和病理生理学的最新进展。

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