Hausmanowa-Petrusewicz I
Zespołu Chorób Nerwowo-Mieśniowych, Polskiej Akademii Nauk, Warszawie.
Neurol Neurochir Pol. 1994 Mar-Apr;28(2):157-66.
In the terminological dictionary of the AAEE conduction block is defined as inability of impulse to pass through a certain point in nerve fibre, although conduction is preserved below that point. Conduction block is manifested as a quantitatively corresponding drop of the amplitude and area of motor evoked potential (MEP) in the distal part in relation to the values of these parameters proximal to the block. Excessive desynchronization of conduction in nerve fibres and certain technical factors should be excluded. Multifocal conduction block is found in many neuropathies, particularly purely motor ones. The probable mechanisms responsible for the difference between motor and sensory nerve fibres with respect to their susceptibility to block development have been discussed. The understanding of conduction block could have important clinical implications, especially in the differential diagnosis of chronic demyelinative neuropathies, in the selection of immunological research methods, in the choice of treatment and prognostication of possible improvement (e.g. in the Guillain-Barre syndrome). Purely motor neuropathy with multifocal conduction block may simulate amyotrophic lateral sclerosis. The development of block in neuropathies is associated frequently with increased level of antibodies against GM1 and the interrelation between these phenomena is not known; the development of block may be due to deposition of GM1 antibodies in internodes or Ranvier's nodes with production of demyelination or with damage to ion channels. Although the concept of conduction block has been introduced in electroneurographic diagnosis there are still many doubts as to the correctness of diagnostic criteria, indispensable technical conditions, and also to the basic problems, such as e.g. 1) is conduction block really limited to acquired neuropathies (its possible occurrence in congenital neuropathies is discussed), 2) why is conduction block not reflecting clinical improvement, 3) in what degree is block reflecting the loss of motor units. These questions are discussed by the author in the light of literature reports and own experience.
在AAEE术语词典中,传导阻滞被定义为冲动无法通过神经纤维的某一点,尽管该点以下的传导功能仍得以保留。传导阻滞表现为运动诱发电位(MEP)在远端部分的幅度和面积相对于阻滞近端这些参数的值出现相应的定量下降。应排除神经纤维传导过度失同步和某些技术因素。多灶性传导阻滞见于许多神经病,尤其是纯运动性神经病。已讨论了运动神经纤维和感觉神经纤维在对阻滞发展的易感性方面存在差异的可能机制。对传导阻滞的理解可能具有重要的临床意义,特别是在慢性脱髓鞘性神经病的鉴别诊断、免疫研究方法的选择、治疗的选择以及对可能改善情况的预后判断(如格林-巴利综合征)方面。伴有多灶性传导阻滞的纯运动性神经病可能酷似肌萎缩侧索硬化症。神经病中阻滞的发生常与抗GM1抗体水平升高有关,而这些现象之间的相互关系尚不清楚;阻滞的发生可能是由于GM1抗体沉积在结间段或郎飞结,导致脱髓鞘或离子通道受损。尽管传导阻滞的概念已被引入神经电生理诊断中,但对于诊断标准的正确性、必不可少的技术条件以及一些基本问题,如:1)传导阻滞是否真的仅限于获得性神经病(讨论了其在先天性神经病中可能的发生情况);2)为什么传导阻滞不能反映临床改善情况;3)阻滞在多大程度上反映运动单位的丧失,仍存在许多疑问。作者根据文献报道和自身经验对这些问题进行了讨论。