Hughes R A, Rees J H
Department of Neurology, UMDS, Guy's Hospital, London, UK.
Curr Opin Neurol. 1994 Oct;7(5):386-92. doi: 10.1097/00019052-199410000-00004.
Guillain-Barré syndrome has now become recognized as a clinical syndrome that may be due to several pathological entities, consisting of an acute inflammatory demyelinating polyradiculoneuropathy as well as an acute motor axonal neuropathy. Campylobacter jejuni infection is a common preceding event and, together with anti-ganglioside GM1 antibodies, is associated with axonal damage and a poor outcome. The mechanism by which such antibodies damage axons is not clear. The Miller Fisher syndrome is very closely associated with antibodies to ganglioside GQ1b that may be important in pathogenesis. Treatment of Guillain-Barré syndrome with intravenous immunoglobulin appears to be as effective as plasma exchange in one controlled trial. Two small series have reported a high incidence of early relapses following intravenous immunoglobulin, and its efficacy is being reexamined in a further controlled trial.
吉兰-巴雷综合征现已被公认为一种临床综合征,它可能由多种病理实体引起,包括急性炎症性脱髓鞘性多发性神经根神经病以及急性运动轴索性神经病。空肠弯曲菌感染是常见的前驱事件,并且与抗神经节苷脂GM1抗体一起,与轴索损伤及不良预后相关。此类抗体损伤轴索的机制尚不清楚。米勒费雪综合征与抗神经节苷脂GQ1b抗体密切相关,该抗体在发病机制中可能起重要作用。在一项对照试验中,静脉注射免疫球蛋白治疗吉兰-巴雷综合征似乎与血浆置换同样有效。两项小型研究系列报告了静脉注射免疫球蛋白后早期复发的高发生率,其疗效正在另一项对照试验中重新评估。