Department of Neurology, Dokkyo Medical University, Tochigi, Japan.
J Neurol Sci. 2012 Aug 15;319(1-2):164-7. doi: 10.1016/j.jns.2012.05.001. Epub 2012 May 31.
Guillain-Barré syndrome can present as demyelinating or axonal subtypes. Recent studies suggest that the neurophysiology of the axonal subtype not only exhibits axonal degeneration but can also show reversible conduction failure at the early stages. It is less certain if reversible conduction failure is evident in only a minority of patients with a specific subtype associated with better prognosis. We describe a 73-year-old man with Guillain-Barré syndrome and electrodiagnostic features of both reversible conduction block and possible axonal degeneration. Initial features of conduction failure were seen in both median nerves. This was followed by features of axonal degeneration, with corresponding weakness in the left abductor pollicis brevis and lumbricalis muscles, which are innervated by the median nerve, but rapid resolution of conduction block with corresponding rapid clinical recovery in the right. The presence of both features in a single patient provides further evidence that early conduction failure can be followed by either rapid resolution or axonal degeneration in the electrophysiological spectrum of axonal Guillain-Barré syndrome.
格林-巴利综合征可表现为脱髓鞘或轴索亚型。最近的研究表明,轴索亚型的神经生理学不仅表现出轴索变性,而且在早期还可能出现传导功能可逆性丧失。在与预后较好的特定亚型相关的少数患者中是否存在这种可逆性传导失败尚不确定。我们描述了一例 73 岁男性,患有格林-巴利综合征和电诊断特征,既有可逆性传导阻滞,也可能有轴索变性。在正中神经中都可以看到传导失败的初始特征。随后出现轴索变性的特征,左侧拇短展肌和蚓状肌(由正中神经支配)出现相应的无力,而右侧的传导阻滞迅速恢复,相应的临床症状也迅速恢复。在单个患者中同时存在这两种特征进一步证明,在轴索格林-巴利综合征的电生理谱中,早期的传导失败之后可能是迅速恢复或轴索变性。