Kinoshita Satoko, Sugie Kazuma, Kataoka Hiroshi, Sugie Miho, Hirano Makito, Ueno Satoshi
Department of Neurology, Nara Medical University School of Medicine, Nara, Japan.
Clin Med Case Rep. 2009 Feb 12;2:17-20. doi: 10.4137/ccrep.s2194. eCollection 2009.
We report the first case of acute autonomic, motor and sensory neuropathy (AASMN) associated with meningoencephalitis. A 62-year-old man presented with fever, neck stiffness, and coma. Respiratory failure developed. Magnetic resonance images showed an abnormality in the medial temporal lobe. Cerebrospinal fluid analysis revealed pleocytosis with a high protein level. Intensive care gradually improved the consciousness level, but paralysis of the four extremities persisted. Nerve conduction studies revealed demyelinating sensory and motor polyneuropathy. Severe orthostatic hypotension, urinary retention, and constipation were also present. Clinical autonomic tests suggested both sympathetic and parasympathetic dysfunction. After intravenous immunoglobulin therapy, motor and sensory symptoms resolved rapidly; dysautonomia resolved gradually over the next 2 months. The response to immunological therapy and the presence of antecedent infection suggest that AASMN is a postinfectious, immune-mediated, autonomic, sensory and motor nervous system dysfunction.
我们报告了首例与脑膜脑炎相关的急性自主神经、运动和感觉神经病(AASMN)。一名62岁男性出现发热、颈部僵硬和昏迷。继而发展为呼吸衰竭。磁共振成像显示颞叶内侧有异常。脑脊液分析显示细胞数增多且蛋白水平升高。重症监护逐渐改善了意识水平,但四肢瘫痪持续存在。神经传导研究显示脱髓鞘性感觉和运动性多发性神经病。还存在严重的体位性低血压、尿潴留和便秘。临床自主神经测试提示交感和副交感神经功能障碍。静脉注射免疫球蛋白治疗后,运动和感觉症状迅速缓解;自主神经功能障碍在接下来的2个月内逐渐缓解。对免疫治疗的反应以及先前感染的存在表明,AASMN是一种感染后、免疫介导的自主神经、感觉和运动神经系统功能障碍。