Department of Neurology, National Taiwan University Hospital, Taipei, Taiwan.
J Neurol Neurosurg Psychiatry. 2011 Apr;82(4):462-5. doi: 10.1136/jnnp.2009.194118. Epub 2010 Jun 15.
A 53-year-old male patient developed insidious onset of length-dependent painful neuropathy on a background of encephalopathy during prolonged treatment with metronidazole for a cumulative dose of 146 g in 88 days. The reversible encephalopathy was documented with gradual resolution of hyperintense lesions in bilateral cerebellum and brainstem on brain MRI together with the improvement in symptoms of ataxia and dysarthria. The concomitant impairment of small-diameter sensory nerves posed a diagnostic challenge. The authors took advantage of serial skin biopsies to demonstrate reversible metronidazole-induced small-fibre sensory neuropathy, that is, skin denervation after metronidazole and corresponding skin reinnervation with the disappearance of sensory symptoms.
一位 53 岁男性患者在因脑病接受长达 88 天的累积剂量为 146g 的甲硝唑治疗后,出现了潜伏性、长度依赖性的痛性多发性神经病。脑 MRI 显示双侧小脑和脑干的高信号病变逐渐消退,共济失调和构音障碍等症状改善,证实了可逆性脑病的存在。同时出现的小直径感觉神经损伤给诊断带来了挑战。作者利用连续的皮肤活检来证明甲硝唑诱导的小纤维感觉神经病是可逆的,即甲硝唑后皮肤去神经支配,以及感觉症状消失后的相应皮肤再神经支配。