炎症性周围神经病的神经超声研究进展

Human Brain Pub Date : 2024-01-10 DOI:10.37819/hb.3.1776
J. Niu, Mingsheng Liu
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摘要

目的:近年来,高分辨率神经超声越来越多地被用作神经传导研究的辅助工具,用于诊断周围神经病。炎症性周围神经病包括一组异质性神经病,主要包括慢性炎症性脱髓鞘性多发性神经病(CIDP)、多灶性运动神经病(MMN)、系统性血管炎性神经病(SVN)和格林-巴利综合征(GBS)。我们描述了不同炎症性神经病的超声波特征。数据来源和研究选择:在 MEDLINE 数据库中搜索有关炎症性周围神经病的神经超声波检查的研究。本综述纳入了截至 2022 年 12 月的研究报告。研究结果在神经病变中,超声波的变化包括神经体积增大、神经回声强度、筋膜直径和血管。大多数 CIDP 患者的 CSA 中度增大,部分患者的 CSA 显著增大,少数患者的 CSA 在正常范围内。由于增大模式不同,超声检查有助于区分 CIDP 和 CMT1。在免疫治疗后的随访中,CIDP 患者的神经 CSA 可能会减小、增大或保持不变。在 MMN 中,紧邻正常节段的区域性肿大占主导地位。在血管炎性神经病中发现了神经增大和高血管化。在 GBS 患者中,周围神经和神经根增大,但在随访时已恢复正常。结论高分辨率神经超声可辅助诊断炎症性周围神经病。CSA 扩大及其分布是评估周围神经最有用、最可量化的参数。对于怀疑患有炎症性神经病变的患者,我们建议测量正中神经、尺神经、C5-8 颈椎根和臂丛中几个预定部位的 CSA。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Progress in the nerve ultrasound of inflammatory peripheral neuropathies
Objective: In recent years, high-resolution nerve ultrasound has been increasingly used as a complementary tool to nerve conduction studies in the diagnosis of peripheral neuropathies. Inflammatory peripheral neuropathies include a heterogeneous group of neuropathies mainly including chronic inflammatory demyelinating polyneuropathies (CIDP), multifocal motor neuropathy (MMN), systemic vasculitic neuropathy (SVN), and Guillain-Barre syndrome (GBS). We describe the ultrasonic characteristics of different inflammatory neuropathies. Data sources and study selection: The MEDLINE database was searched to find studies on nerve sonography in inflammatory peripheral neuropathies. Reported studies up to December 2022 were included in this review. Results: In neuropathies, the changes in ultrasound include enlarged nerve size, nerve echo-intensity, fascicle diameter and vascularity. Most CIDP patients have moderately enlarged CSA, some have dramatically enlarged CSA, and few have CSA within the normal range. Since the enlargement patterns are different, ultrasound is useful to help differentiate CIDP from CMT1. In follow-ups after immune treatment, nerve CSAs in CIDP could decrease, increase, or remain unchanged. Regional enlargement next to normal segments predominated in MMN. Nerve enlargement and hyper vascularization were found in vasculitic neuropathy. In GBS patients, there were enlarged peripheral nerve and nerve roots, which became normal at follow-up. Conclusions: High-resolution nerve ultrasound is complementary to the diagnosis of inflammatory peripheral neuropathies. CSA enlargement and its distribution are the most useful and quantifiable parameters in the evaluation of peripheral nerves. For patients suspected to have inflammatory neuropathies, we advise measuring the CSA of several pre-determined sites in the median, ulnar nerve, C5-8 cervical roots, and brachial plexus.
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