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首页> 外文期刊>Vojnosanitetski Pregled >Diagnostic value of combined magnetic resonance imaging examination of brachial plexus and electrophysiological studies in multifocal motor neuropathy
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Diagnostic value of combined magnetic resonance imaging examination of brachial plexus and electrophysiological studies in multifocal motor neuropathy

机译:臂丛神经核磁共振成像联合电生理检查对多灶性运动神经病的诊断价值

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Background/Aim. Multifocal motor neuropathy (MMN) is an immune-mediated disorder characterized by slowly progressive asymetrical weakness of limbs without sensory loss. The objective of this study was to investigate the involvement of brachial plexus using combined cervical magnetic stimulation and magnetic resonance imaging (MRI) of plexus brachialis in patients with MMN. We payed special attention to the nerve roots forming nerves inervating weak muscles, but without detectable conduction block (CB) using conventional nerve conduction studies. Methods. Nine patients with proven MMN were included in the study. In all of them MRI of the cervical spine and brachial plexus was performed using a Siemens Avanto 1.5 T unit, applying T1 and turbo spinecho T1 sequence, axial turbo spin-echo T2 sequence and a coronal fat-saturated turbo spin-echo T2 sequence. Results. In all the patients severe asymmetric distal weakness of muscles inervated by radial, ulnar, median and peroneal nerves was observed and the most striking presentation was bilateral wrist and finger drop. Three of them had additional proximal weakness of muscles inervated by axillar and femoral nerves. The majority of the patients had slightly increased cerebrospinal fluid (CSF) protein content. Six of the patients had positive serum polyclonal IgM anti-GM1 antibodies. Electromyoneurography (EMG) showed neurogenic changes, the most severe in distal muscles inervated by radial nerves. All the patients had persistent partial CBs outside the usual sites of nerve compression in radial, ulnar, median and peroneal nerves. In three of the patients cervical magnetic stimulation suggested proximal CBs between cervical root emergence and Erb’s point (prolonged motor root conduction time). In all the patients T2-weighted MRI revealed increased signal intensity in at least one cervical root, truncus or fasciculus of brachial plexus. Conclusion. We found clinical correlation between muscle weakness, prolonged motor root conduction time and MRI abnormalities of the brachial plexus, which was of the greatest importance in the nerves without CB inervating weak muscles.
机译:背景/目标。多灶性运动神经病(MMN)是一种免疫介导的疾病,其特征是四肢缓慢进行性不对称性无力,无感觉丧失。这项研究的目的是调查合并MMN患者臂丛神经的颈椎磁刺激和磁共振成像(MRI)的臂丛神经受累情况。我们特别注意了神经根,神经形成了神经,使肌无力,但使用常规的神经传导研究却没有可检测到的传导阻滞(CB)。方法。该研究包括9名MMN证实患者。所有患者均使用Siemens Avanto 1.5 T装置对T1和Turbo Spinecho T1序列,轴向Turbo Spin-Echo T2序列和冠状脂肪饱和Turbo Spin-Echo T2序列进行了颈椎和臂丛神经的MRI检查。结果。在所有患者中,均观察到严重的不对称远端肌无力,其radial神经,尺神经,正中神经和腓神经受神经支配,最引人注目的表现是双侧手腕和手指掉落。其中三个有腋窝和股神经支配的肌肉的近端无力。大多数患者的脑脊液(CSF)蛋白含量略有增加。其中六名患者的血清多克隆IgM抗GM1抗体阳性。肌电图(EMG)显示神经源性变化,在radial神经侵犯的远端肌肉中最为严重。所有患者均在radial神经,尺神经,正中神经和腓神经的神经压迫部位之外出现持续的部分CB。在三名患者中,子宫颈磁刺激提示子宫颈根部出现与Erb点(延长的运动根传导时间)之间的近端CB。在所有患者中,T2加权MRI至少显示了臂丛神经的一根颈根,截臂或筋膜中的信号强度增加。结论。我们发现肌无力,延长的运动根传导时间和臂丛神经MRI异常之间存在临床相关性,这在没有CB肌无力肌力的神经中最为重要。

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