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[重症肌无力及其他神经肌肉疾病中的单纤维肌电图]

[Single fiber electromyogram in myasthenia gravis and other neuromuscular diseases].

作者信息

Nogués M A, Rivero A, Stalberg E

机构信息

Instituto de Investigaciones Neurológicas Dr. Raúl Carrea (FLENI), Buenos Aires, Argentina.

出版信息

Medicina (B Aires). 1991;51(4):307-14.

PMID:1668291
Abstract

Single fibre electromyography (SFEMG) has been used to study neuromuscular transmission and the degree of reinnervation in patients with myasthenia gravis (MG) (n = 70); Lambert-Eaton syndrome (n = 3); myopathies (n = 8); motor neuron disease (n = 4) and peripheral neuropathies (n = 3) (Table 1). An automatic method was used to calculate neuromuscular jitter by means of a PC computer, a TECA TD 20 electromyograph and a jittermeter. Twenty pairs of potentials were selected from the extensor digitorum communis muscle for analysis using a trigger unit and a delay line. Mean jitter and percentage of pairs with normal and abnormal jitter were calculated (Figs. 1 and 2). MG patients showed pairs with normal (Fig. 3) and other with abnormal jitter and intermittent blocking (Fig. 4). Abnormalities were found in 72% of patients with ocular MG, in 95% with mild generalized MG, in 93% with moderate generalized MG and in 100% of severe MG cases (Table 2), (Fig. 5). There was a significant correlation between patient disability and jitter values (Fig. 6). The method was useful for the follow-up during immunosuppressant treatment (Fig. 7). Patients with other myopathies showed normal or mildly increased jitter and increased fibre density. The most common abnormality in patients with neurogenic conditions was increased fibre density, which ranged from 2.1 to 4.3 (Figs. 8 and 9). The method used showed high sensitivity for the detection of neuromuscular transmission defects. In some cases an abnormal jitter was found even before the appearance of transmission block and therefore it was possible to find abnormalities in clinically normal muscle.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

单纤维肌电图(SFEMG)已被用于研究重症肌无力(MG)(n = 70)、兰伯特-伊顿综合征(n = 3)、肌病(n = 8)、运动神经元病(n = 4)和周围神经病(n = 3)患者的神经肌肉传递及再支配程度(表1)。采用一种自动方法,借助个人计算机、TECA TD 20肌电图仪和抖动仪来计算神经肌肉抖动。从指总伸肌中选取20对电位,使用触发装置和延迟线进行分析。计算平均抖动以及抖动正常和异常的电位对百分比(图1和图2)。MG患者中有些电位对抖动正常(图3),另一些则抖动异常并伴有间歇性阻滞(图4)。在眼肌型MG患者中,72%存在异常;轻度全身型MG患者中,95%存在异常;中度全身型MG患者中,93%存在异常;重度MG患者中,100%存在异常(表2,图5)。患者的残疾程度与抖动值之间存在显著相关性(图6)。该方法对免疫抑制剂治疗期间的随访很有用(图7)。其他肌病患者的抖动正常或轻度增加,纤维密度增加。神经源性疾病患者最常见的异常是纤维密度增加,范围为2.1至4.3(图8和图9)。所采用的方法对神经肌肉传递缺陷的检测具有高敏感性。在某些情况下,甚至在出现传递阻滞之前就发现了异常抖动,因此有可能在临床正常的肌肉中发现异常。(摘要截取自250词)

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