Leventoglu Alev, Ozlu Pelin, Ince Ferda
Department of Neurology, Ufuk University Medical School, Ankara, Turkey.
Case Rep Neurol Med. 2013;2013:489451. doi: 10.1155/2013/489451. Epub 2013 Oct 23.
Many cases of atopic myelitis have been reported in Japan; however very few were described in western countries. An 82-year-old woman with a past medical history of atopic dermatitis and asthma presented with progressive paresthesia (tingling) of both hands and tetraparesis. Before the onset of neurological symptoms, she complained of ichthyosis of both legs for 5 weeks. Magnetic resonance imaging demonstrated multisegmental degenerative arthritis, degenerative disc disease, and abnormal spinal cord signal intensity over several cervical segments, suggesting the diagnosis of myelitis. Total serum IgE level was elevated. Nerve conduction studies revealed asymmetric axonal sensorimotor neuropathy. The cerebrospinal fluid specimen showed lymphocytic pleocytosis and elevated protein level. Based on clinical, imaging, and laboratory findings, atopic myelitis was diagnosed. The diagnosis of atopic myelitis should be considered in myelopathy patients with history of atopy and elevated serum IgE levels.
日本已报告了许多特应性脊髓炎病例;然而,西方国家对此的描述却非常少。一名82岁女性,有特应性皮炎和哮喘病史,出现双手进行性感觉异常(刺痛)和四肢轻瘫。在神经症状出现之前,她双腿鱼鳞病已有5周。磁共振成像显示多节段退行性关节炎、椎间盘退变以及多个颈椎节段脊髓信号强度异常,提示脊髓炎诊断。血清总IgE水平升高。神经传导研究显示不对称性轴索性感觉运动神经病。脑脊液标本显示淋巴细胞增多和蛋白水平升高。根据临床、影像学和实验室检查结果,诊断为特应性脊髓炎。对于有特应性病史且血清IgE水平升高的脊髓病患者,应考虑特应性脊髓炎的诊断。