Li Xiang, Lin Jie, Pan Sipei, Weng Yiyun, Li Jia, Zhang Xu, Xia Junhui, Tong Qiaowen
Department of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, ,China.
Department of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, ,China.
J Neuroimmunol. 2017 Aug 15;309:68-71. doi: 10.1016/j.jneuroim.2017.05.013. Epub 2017 May 22.
A rare case of neuromyelitis optica spectrum disorder, suspected to be bacterial meningomyelitis as the initial manifestation, is reported. The patient presented with initial symptoms of meningomyelitis and fever. Cerebrospinal fluid analysis revealed pleocytosis (1280×10/L [98% lymphocytes]) and glucose level of 1.8mmol/L. Magnetic resonance imaging revealed >3 vertebral, longitudinally extensive transverse myelitis and area postrema lesions. Right optic neuritis was experienced 20months after the first attack. Serum anti-aquaporin-4 antibody was positive, and a diagnosis of neuromyelitis optica spectrum disorder was made, supporting the hypothesis that the pathogenesis of neuromyelitis optica is triggered by infection.
报告了1例视神经脊髓炎谱系障碍罕见病例,最初表现疑似为细菌性脑脊膜炎。患者最初出现脑脊膜炎症状和发热。脑脊液分析显示细胞增多(1280×10/L[98%为淋巴细胞]),葡萄糖水平为1.8mmol/L。磁共振成像显示超过3个椎体出现纵向广泛横贯性脊髓炎和最后区病变。首次发作20个月后出现右眼视神经炎。血清抗水通道蛋白4抗体呈阳性,诊断为视神经脊髓炎谱系障碍,支持视神经脊髓炎发病机制由感染触发的假说。