Basta Ivana, Nikolić Ana, Apostolski Slobodan, Lavrnić Slobodan, Stosić-Opinćal Tatjana, Banjalić Sandra, Knezević-Apostolski Sladana, Ilić Tihomir V, Marjanović Ivan, Milićev Milena, Lavrnić Dragana
Vojnosanit Pregl. 2014 Aug;71(8):723-9. doi: 10.2298/vsp1408723b.
BACKGROUND/AIM: Multifocal motor neuropathy (MMN) is an immune-mediated disorder characterised 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.
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 spin-echo T1 sequence, axial turbo spin-echo T2 sequence and a coronal fat-saturated turbo spin-echo T2 sequence.
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.
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.
背景/目的:多灶性运动神经病(MMN)是一种免疫介导的疾病,其特征为四肢进行性不对称无力且无感觉丧失。本研究的目的是通过联合颈部磁刺激和臂丛磁共振成像(MRI)来研究MMN患者臂丛神经的受累情况。我们特别关注支配无力肌肉的神经根,这些神经根在常规神经传导研究中未检测到传导阻滞(CB)。
9例确诊为MMN的患者纳入本研究。对所有患者均使用西门子Avanto 1.5 T设备进行颈椎和臂丛神经的MRI检查,采用T1加权成像和快速自旋回波T1序列、轴位快速自旋回波T2序列以及冠状位脂肪抑制快速自旋回波T2序列。
所有患者均观察到由桡神经、尺神经、正中神经和腓总神经支配的肌肉出现严重不对称性远端无力,最显著的表现为双侧腕下垂和指下垂。其中3例患者还存在由腋神经和股神经支配的肌肉近端无力。大多数患者脑脊液(CSF)蛋白含量略有升高。6例患者血清多克隆IgM抗GM1抗体呈阳性。肌电图(EMG)显示为神经源性改变,以桡神经支配的远端肌肉最为严重。所有患者在桡神经、尺神经、正中神经和腓总神经的常见神经受压部位以外均存在持续性部分CB。3例患者的颈部磁刺激提示在颈神经根穿出至Erb点之间存在近端CB(运动神经根传导时间延长)。所有患者的T2加权MRI显示至少一条颈神经根、臂丛神经干或束的信号强度增加。
我们发现肌肉无力、运动神经根传导时间延长与臂丛神经MRI异常之间存在临床相关性,这对于支配无力肌肉但无CB的神经最为重要。