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格林-巴利综合征。

Guillain-Barré syndrome.

机构信息

Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.

Department of Neurology, Erasmus MC, University Medical Center, Rotterdam, Netherlands; Department of Immunology, Erasmus MC, University Medical Center, Rotterdam, Netherlands.

出版信息

Lancet. 2016 Aug 13;388(10045):717-27. doi: 10.1016/S0140-6736(16)00339-1. Epub 2016 Mar 2.

Abstract

Guillain-Barré syndrome is the most common and most severe acute paralytic neuropathy, with about 100,000 people developing the disorder every year worldwide. Under the umbrella term of Guillain-Barré syndrome are several recognisable variants with distinct clinical and pathological features. The severe, generalised manifestation of Guillain-Barré syndrome with respiratory failure affects 20-30% of cases. Treatment with intravenous immunoglobulin or plasma exchange is the optimal management approach, alongside supportive care. Understanding of the infectious triggers and immunological and pathological mechanisms has advanced substantially in the past 10 years, and is guiding clinical trials investigating new treatments. Investigators of large, worldwide, collaborative studies of the spectrum of Guillain-Barré syndrome are accruing data for clinical and biological databases to inform the development of outcome predictors and disease biomarkers. Such studies are transforming the clinical and scientific landscape of acute autoimmune neuropathies.

摘要

格林-巴利综合征是最常见和最严重的急性弛缓性神经病,全世界每年约有 10 万人患病。在格林-巴利综合征这一总称下,有几种可识别的变异型,具有不同的临床和病理特征。伴有呼吸衰竭的严重、全身性格林-巴利综合征影响 20-30%的病例。静脉注射免疫球蛋白或血浆置换联合支持治疗是最佳的治疗方法。在过去 10 年中,人们对感染触发因素以及免疫和病理机制的理解有了很大的进展,这为探索新治疗方法的临床试验提供了指导。对格林-巴利综合征谱进行大型、全球性合作研究的调查人员正在为临床和生物数据库积累数据,以告知预后预测因子和疾病生物标志物的开发。这些研究正在改变急性自身免疫性神经病的临床和科学格局。

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