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[束内神经成像在评估轴突退变方面优于传统神经传导研究]

[Superiority of intrafascicular neurography over conventional nerve conduction studies in evaluating axonal degeneration].

作者信息

Hasegawa O, Matsumoto S, Iino M, Kurita R, Yoshii T

机构信息

Department of Neurology, Yokohama City University School of Medicine, Fukuura, Japan.

出版信息

No To Shinkei. 1999 Apr;51(4):313-6.

Abstract

We investigated conventional motor and sensory nerve conduction studies (MCS & SCS) with regard to the sensitivity in detecting axonopathies. Twelve patients with axonal type of polyneuropathy, 2 vincristin neuropathy and 10 cisplatin neuropathy, were examined by MCS & SCS. Their data were compared with those by intrafascicular microneurography (MNG) of the median nerve. Nerve conduction velocities were within normal limits or slightly reduced to 87-99% of the normal. Amplitude of compound muscle action potential (CMAP) by MCS decreased to 4 or 5 mV in vincristin neuropathy, though cisplatin neuropathy presented normal amplitude. Amplitude of sensory nerve action potential (SNAP) by SCS was undetected in one median nerve and in three sural nerves. While, compound nerve action potential (CNAP) by MNG was all recorded, and presented the amplitude value of below 150 microV in seven patients. The waveform was normal or mild neuropathic pattern. No patients presented normal CNAP amplitude and reduced SNAP amplitude. But there were three patients who had normal SNAP amplitude and reduced CNAP amplitude. In SCS we could recognize abnormal only after CNAP amplitude by MNG dropped to below 100 microV. Cisplatin neuropathy demonstrates reduction of CNAP or SNAP amplitude, and vincristin neuropathy further presents reduction of CMAP amplitude. Evaluation of axonopathy is best achieved by nerve action potential amplitude. Conventional surface electrode methods are available for this purpose, but MNG is more sensitive and is capable of quantitative analysis even in severely damaged nerves.

摘要

我们研究了传统的运动和感觉神经传导研究(MCS和SCS)在检测轴索性神经病方面的敏感性。对12例轴索性多神经病患者、2例长春新碱神经病患者和10例顺铂神经病患者进行了MCS和SCS检查。将他们的数据与正中神经束膜内微神经电图(MNG)的数据进行比较。神经传导速度在正常范围内或略有降低至正常的87 - 99%。MCS检测的复合肌肉动作电位(CMAP)幅度在长春新碱神经病中降至4或5 mV,而顺铂神经病的幅度正常。SCS检测的感觉神经动作电位(SNAP)幅度在一条正中神经和三条腓肠神经中未检测到。同时,MNG记录的复合神经动作电位(CNAP)均被记录,7例患者的幅度值低于150 μV。波形正常或呈轻度神经病变模式。没有患者出现CNAP幅度正常而SNAP幅度降低的情况。但有3例患者SNAP幅度正常而CNAP幅度降低。在SCS中,只有当MNG检测的CNAP幅度降至低于100 μV时,我们才能识别异常。顺铂神经病表现为CNAP或SNAP幅度降低,长春新碱神经病进一步表现为CMAP幅度降低。评估轴索性神经病最好通过神经动作电位幅度来实现。传统的表面电极方法可用于此目的,但MNG更敏感,即使在严重受损的神经中也能够进行定量分析。

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