Metronidazole-induced toxicity of the central and peripheral nervous system.

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL
Diego Villagrán Sancho, Carlota Villar Rodríguez, Antonio Cristóbal Luque Ambrosiani, Pablo Baena-Palomino
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引用次数: 0

Abstract

A woman in her 80s was admitted with a growing feeling of dizziness, tingling and vomiting that began a week before. The neurological examination showed dysarthria, downbeat nystagmus and gait ataxia. At the time, she was taking antibiotics (1 g amoxicillin and 500 mg metronidazole every 8 hours) following surgery for a mandibular abscess a month earlier.Brain MRI showed T2 and FLAIR hyperintensities in dentate nuclei and splenium of the corpus callosum, findings described in metronidazole neurotoxicity. Metronidazole was discontinued, with resolution of all symptoms except lower limb paraesthesias.Given the ageing population and the increasing use of pharmacological treatments for multiple conditions, drug-induced neurological complications are receiving growing attention, yet they often remain underrecognised. Metronidazole neurotoxicity is a rare adverse effect that should be considered especially during prolonged treatments. The most frequent debut resembles this case, with cerebellar dysfunction as the most common central nervous system toxicity and concomitant polyneuropathy frequently associated.

甲硝唑对中枢和周围神经系统的毒性作用。
一名80多岁的妇女在一周前开始感到越来越头晕、刺痛和呕吐。神经学检查显示构音障碍、下拍性眼球震颤和步态共济失调。当时,她在一个月前的下颌脓肿手术后服用抗生素(每8小时服用1克阿莫西林和500毫克甲硝唑)。脑MRI显示胼胝体齿状核和脾部的T2和FLAIR高信号,结果描述为甲硝唑神经毒性。停用甲硝唑,除下肢感觉异常外所有症状均消失。鉴于人口老龄化和对多种疾病越来越多地使用药物治疗,药物引起的神经系统并发症正受到越来越多的关注,但它们往往仍未得到充分认识。甲硝唑神经毒性是一种罕见的不良反应,特别是在长期治疗期间应予以考虑。最常见的首发病例类似于本病例,最常见的中枢神经系统毒性为小脑功能障碍,并常伴有多发性神经病变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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