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Case Reports
. 2021 Mar 18;25(1):2016.
doi: 10.4102/sajr.v25i1.2016. eCollection 2021.

Metronidazole-induced encephalopathy

Affiliations
Case Reports

Metronidazole-induced encephalopathy

Vikash G Lala et al. SA J Radiol. .

Abstract

Metronidazole is a widely used antibacterial and antiprotozoal agent for a number of conditions. Whilst its more common gastrointestinal side effects are well known, neurotoxicity remains under-recognised. Both central and peripheral neurological side effects have been described. This report describes a case of radiologically confirmed metronidazole-induced cerebellar ataxia in a cirrhotic patient with a review of the literature. Awareness of this side effect is essential for prompt recognition as early drug withdrawal leads to resolution in the majority of cases.

Keywords: corpus callosum lesions; dentate nucleus lesions; metronidazole; metronidazole adverse events; metronidazole-induced cerebellar ataxia; metronidazole-induced encephalopathy; metronidazole-induced neurotoxicity; splenium lesions.

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Conflict of interest statement

The authors declare that they have no financial or personal relationships that may have inappropriately influenced them in writing this article.

Figures

FIGURE 1
FIGURE 1
Fluid attenuated inversion recovery (a) and T2 turbospin echo sequence (b) demonstrating high signal intensity in the dentate nuclei bilaterally (white arrows).
FIGURE 2
FIGURE 2
Diffusion-weigthed imaging (a) indicating increased signal in the splenium of the corpus callosum and corresponding apparent diffusion coefficient map (b) showing a decreased signal in this area in keeping with restriction.
FIGURE 3
FIGURE 3
Fluid attenuated inversion recovery imaging at the 7-week follow-up imaging, demonstrating resolution of the previous dentate nuclei high signal; compare with Figure 1.
FIGURE 4
FIGURE 4
(a) Diffusion sequence showing resolution of the splenium lesion at follow up (b) Apparent diffusion coefficient map showing complete resolution of the splenium lesion at follow up imaging; compare with Figure 2.

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