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后骨间神经综合征和多灶性运动神经病的桡侧运动神经传导研究

Radial motor nerve conduction study in posterior interosseous nerve syndrome and multifocal motor neuropathy.

作者信息

Baima José Pedro S, Heise Carlos Otto

机构信息

Universidade de São Paulo, Departamento de Neurologia, São Paulo SP, Brazil.

Universidade Federal do Ceará, Unidade do Sistema Nervoso, Fortaleza CE, Brazil.

出版信息

Arq Neuropsiquiatr. 2025 Feb;83(2):1-5. doi: 10.1055/s-0045-1806818. Epub 2025 Apr 27.

Abstract

BACKGROUND

Finger extension weakness could be a presentation of either posterior interosseous nerve (PIN) syndrome or multifocal motor neuropathy (MMN). However, there is a delay in the diagnosis of MMN in cases with a selective radial weakness, as they are frequently misdiagnosed as PIN.

OBJECTIVE

To analyze which variables in nerve conduction studies could aid in the early diagnosis of MMN.

METHODS

We reviewed charts of patients with diagnoses of MMN or PIN syndrome, from 2014 to 2022, in a single Brazilian reference center. Electrophysiological parameters included in the analysis were motor conduction velocity (CV), the presence and magnitude of conduction block (CB), distal motor latencies (DML), and the compound muscle action potential amplitude (CMAP) of the affected radial nerve.

RESULTS

A total of 44 radial nerves were included in the study. Axonal loss was associated with a diagnosis of PIN syndrome, while conduction block was associated with MMN ( < 0.05). No patient with PIN had a CB over 60%, while 7 out of 12 radial CB blocks in patients with MMN were above that. Axonal degeneration was present in 4 MMN patients and in all patients with PIN syndrome. There was no difference in CV and DML between groups.

CONCLUSION

The presence of CB or the absence of distal CMAP amplitude reduction should lead physicians to consider MMN, and a comprehensive nerve conduction study should be performed.

摘要

背景

手指伸展无力可能是骨间后神经(PIN)综合征或多灶性运动神经病(MMN)的表现。然而,在选择性桡神经无力的病例中,MMN的诊断存在延迟,因为它们经常被误诊为PIN。

目的

分析神经传导研究中的哪些变量有助于MMN的早期诊断。

方法

我们回顾了2014年至2022年在巴西一个参考中心诊断为MMN或PIN综合征的患者病历。分析中包括的电生理参数有运动传导速度(CV)、传导阻滞(CB)的存在及程度、远端运动潜伏期(DML)以及受影响桡神经的复合肌肉动作电位幅度(CMAP)。

结果

该研究共纳入44条桡神经。轴突损失与PIN综合征的诊断相关,而传导阻滞与MMN相关(<0.05)。PIN患者中没有CB超过60%的情况,而MMN患者的12条桡神经CB阻滞中有7条高于该值。4例MMN患者和所有PIN综合征患者均存在轴突变性。两组之间的CV和DML没有差异。

结论

CB的存在或远端CMAP幅度未降低应促使医生考虑MMN,并应进行全面的神经传导研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/898c/12034393/2d5c4dce8c69/10-1055-s-0045-1806818-i240319-1.jpg

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