鉴别多灶性运动神经病与卡压神经病-诊断挑战

R. Rison, S. Beydoun
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引用次数: 2

摘要

多灶性运动神经病(MMN)是一种罕见的免疫介导的神经肌肉疾病,其特征是周围运动神经受损,导致肌肉无力,对手臂的影响大于腿部。该疾病以前被称为MMN伴传导阻滞(MMNCB),因为其主要特征是沿运动神经的多个部位发生CB,尽管在早期阶段轴突不受影响。由于各种因素,包括解剖结构、纤维-骨隧道、韧带、局部水肿、肿瘤、糖尿病、药物、关节炎、甲状腺功能减退、肥胖或重复运动,当身体各个部位的单个神经受到慢性压迫或机械损伤时,就会发生神经受压。神经压迫在受影响的解剖区域引起感觉症状,如感觉异常、麻木、感觉障碍、肌肉无力和萎缩(如果未经治疗)。单个或多个神经受累可能与MMN的一些运动症状相似,因此,在其早期阶段,可能混淆这两种情况,这可能导致严重的临床后果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differentiating Multifocal Motor Neuropathy from Entrapment Neuropathy—A Diagnostic Challenge
TOUCH MEDICAL MEDIA 17 Multifocal motor neuropathy (MMN) is a rare, immune-mediated neuromuscular condition characterized by impairment of the peripheral motor nerves, leading to muscle weakness, affecting the arms more than the legs. The disease was formerly known as MMN with conduction block (MMNCB), since a predominant feature is CB at multiple sites along the motor nerves, although at early stages the axons are not affected. Entrapment neuropathy (EN) occurs when single nerves in various body locations become chronically compressed or mechanically injured as a result of various factors, including anatomical structures, fibro-osseous tunnels, ligaments, local edema, tumors, diabetes, medications, arthritis, hypothyroidism, obesity, or repetitive movements. Nerve compression causes sensory symptoms, such as paresthesias, numbness, dysesthesias, muscle weakness, and atrophy (if untreated), in the affected anatomical area. The involvement of a single or more than one nerve can resemble some of the motor symptoms of MMN, and consequently, in its early stages, it is possible to confuse the two conditions, which can have serious clinical consequences.
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