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Pulmonary Vasculitis

机译:肺血管炎

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摘要

Pulmonary vasculitis is an uncommon but potentially lethal disorder which may cause complications in diverse systemic vasculitis disorders. The most common pulmonary vasculitides, which include Wegener's granulomatosis, microscopic polyangi-itis, and Churg-Strauss syndrome, are discussed in detail here. These three vasculitic disorders are associated with circulating antibodies directed against the cytoplasmic components of neutrophils and monocytes (ANCA). Treatment with corticos-teroids and immunosuppressive or cytotoxic agents is highly effective against each of these entities, with response rates of 70-95%. We briefly discuss other rare disorders that may involve pulmonary vessels including bronchocentric granulomatosis, necrotizing sarcoid angiitis, lymphomatoid granulomatosis, Behcet disease, and Takayasu's arteritis.
机译:肺血管炎是一种罕见但潜在的致死性疾病,可能引起多种系统性血管炎疾病的并发症。此处详细讨论最常见的肺血管炎,包括韦格纳肉芽肿病,微观多发性血管炎和楚格-史特劳斯综合征。这三种血管性疾病与针对中性粒细胞和单核细胞(ANCA)的胞质成分的循环抗体有关。用皮质类固醇和免疫抑制剂或细胞毒剂治疗对这些实体中的每一个都是非常有效的,反应率为70-95%。我们简要讨论了可能涉及肺血管的其他罕见疾病,包括支气管中心性肉芽肿病,坏死性结节性血管炎,淋巴瘤样肉芽肿病,白塞病和Takayasu的动脉炎。

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