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韦格纳肉芽肿病的临床表现与治疗。

Clinical manifestations and treatment of Wegener's granulomatosis.

机构信息

Department of Rheumatology and Clinical Immunology, Vasculitis Center, University Hospital Schleswig-Holstein, Bad Bramstedt, 24576 Bad Bramstedt, Germany.

出版信息

Rheum Dis Clin North Am. 2010 Aug;36(3):507-26. doi: 10.1016/j.rdc.2010.05.008.

Abstract

Wegener's granulomatosis (WG) is characterized by granulomatous lesions and vasculitic disease manifestations. Granulomatous lesions are found in the upper and lower respiratory tract (eg, granulomatous sinusitis, orbital masses, and pulmonary granuloma), whereas vasculitic manifestations occur frequently in lung (alveolar hemorrhage) and kidney (glomerulonephritis). Vasculitis is typically associated with antineutrophil cytoplasmic antibodies (ANCA) directed against proteinase 3. WG has been traditionally associated with a poor outcome and increased mortality as documented by numerous studies; however, recent cohort studies report an improved outcome, probably a consequence of increased awareness leading to an earlier diagnosis, and to improved treatment strategies derived from evidence from controlled trials. Treatment regimens for WG, adapted to disease stage and activity, are reviewed and discussed in this article.

摘要

韦格纳肉芽肿(WG)的特征是肉芽肿性病变和血管炎表现。肉芽肿性病变在上呼吸道和下呼吸道均可出现(如肉芽肿性鼻窦炎、眼眶肿块和肺部肉芽肿),而血管炎表现常发生在肺部(肺泡出血)和肾脏(肾小球肾炎)。血管炎通常与针对蛋白酶 3 的抗中性粒细胞胞质抗体(ANCA)相关。WG 传统上与预后不良和死亡率增加相关,这在许多研究中都有记录;然而,最近的队列研究报告了更好的结果,这可能是由于提高了认识,导致更早的诊断,以及从对照试验中获得的证据改进了治疗策略。本文回顾和讨论了适应疾病阶段和活动度的 WG 治疗方案。

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