Department of Neurology, University of Kansas Medical Center, 3599 Rainbow Boulevard, Mail Stop 2012, Kansas City, KS 66160, USA.
Neurol Clin. 2013 May;31(2):491-510. doi: 10.1016/j.ncl.2013.01.005. Epub 2013 Feb 19.
Guillain-Barré syndrome (GBS) is characterized by rapidly evolving ascending weakness, mild sensory loss, and hyporeflexia or areflexia. Acute inflammatory demyelinating polyneuropathy was the first to be recognized over a century ago and is the most common form of GBS. Axonal motor and sensorimotor variants have been described in the last three decades and are mediated by molecular mimicry targeting peripheral nerve motor axons. Other rare phenotypic variants have been recently described with pure sensory variant, restricted autonomic manifestations, and the pharyngeal-cervical-brachial pattern. It is important to recognize GBS and its variants because of the availability of equally effective therapies in the form of plasmapheresis and intravenous immunoglobulins.
格林-巴利综合征(GBS)的特征是迅速进展的上行性无力、轻度感觉丧失以及反射减弱或消失。急性炎性脱髓鞘性多发性神经病在一个多世纪前首先被认识,是 GBS 最常见的形式。过去三十年中描述了轴索性运动和运动感觉混合性神经病,其介导机制是针对周围神经运动轴突的分子模拟。最近还描述了其他罕见的表型变异,包括纯感觉变异型、局限自主神经表现型和咽-颈-臂型。由于可采用血浆置换和静脉注射免疫球蛋白等同样有效的治疗方法,因此识别 GBS 及其变异型非常重要。