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多灶性运动神经病。

Multifocal motor neuropathy.

机构信息

Department of Neurology, University of Michigan Health System, Ann Arbor, MI 48109-5036, USA.

出版信息

Semin Neurol. 2012 Nov;32(5):500-5. doi: 10.1055/s-0033-1334468. Epub 2013 May 15.

DOI:10.1055/s-0033-1334468
PMID:23677657
Abstract

Multifocal motor neuropathy is an acquired disorder in which demyelination of motor axons, presumably due to autoimmune attack, results in progressive painless weakness without sensory loss. Motor axonal damage also occurs. It is a frequent mimic of motor neuron disease. Recognition of multifocal motor neuropathy is critical because it tends to be very responsive to treatment. Infusion of intravenous immunoglobulin is the initial treatment of choice, but other immunosuppressive treatments may also be effective. It appears that corticosteroids produce minimal benefit.

摘要

多灶性运动神经病是一种获得性疾病,其运动轴突脱髓鞘,推测是由于自身免疫攻击所致,导致进行性无痛性无力而无感觉丧失。运动轴突损伤也会发生。它是运动神经元病的常见模拟疾病。识别多灶性运动神经病非常重要,因为它往往对治疗反应良好。静脉注射免疫球蛋白是首选的初始治疗方法,但其他免疫抑制治疗也可能有效。皮质类固醇似乎益处极小。

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Multifocal motor neuropathy.多灶性运动神经病。
Semin Neurol. 2012 Nov;32(5):500-5. doi: 10.1055/s-0033-1334468. Epub 2013 May 15.
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Axonal multifocal motor neuropathy without conduction block or other features of demyelination.无传导阻滞或其他脱髓鞘特征的轴索性多灶性运动神经病
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Axonal multifocal neuropathy without conduction block or other features of demyelination.无传导阻滞或其他脱髓鞘特征的轴索性多灶性神经病
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Human immune globulin infusion in the management of multifocal motor neuropathy.
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Intravenous immunoglobulin for maintenance treatment of multifocal motor neuropathy: A multi-center, open-label, 52-week phase 3 trial.静脉注射免疫球蛋白治疗多灶性运动神经病的维持治疗:一项多中心、开放标签、52 周 3 期临床试验。
J Peripher Nerv Syst. 2018 Jun;23(2):115-119. doi: 10.1111/jns.12268. Epub 2018 Apr 24.
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Multifocal motor neuropathy: a review of pathogenesis, diagnosis, and treatment.多灶性运动神经病:发病机制、诊断与治疗综述
Neuropsychiatr Dis Treat. 2014 Apr 5;10:567-76. doi: 10.2147/NDT.S39592. eCollection 2014.