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MRI Findings and Topographic Distribution of Lesions in Metronidazole-Induced Encephalopathy

Purpose This study aims to describe the magnetic resonance imaging (MRI) of the brain of five patients diagnosed with metronidazole-induced encephalopathy (MIE). In addition, the aim of our study was to better define the topographic distribution of lesions in MIE. Methods We retrospectively evaluate...

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Autores principales: Fatima, Ambreen, Khanduri, Sachin, Sultana, Sadaf, ., Surbhi, Siddiqui, Saim A, Gupta, Ashkrit, Pathak, Vaibhav, Mulani, Mohsin, Khan, Salma, Bansal, Tanya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9573127/
https://www.ncbi.nlm.nih.gov/pubmed/36282977
http://dx.doi.org/10.7759/cureus.29145
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author Fatima, Ambreen
Khanduri, Sachin
Sultana, Sadaf
., Surbhi
Siddiqui, Saim A
Gupta, Ashkrit
Pathak, Vaibhav
Mulani, Mohsin
Khan, Salma
Bansal, Tanya
author_facet Fatima, Ambreen
Khanduri, Sachin
Sultana, Sadaf
., Surbhi
Siddiqui, Saim A
Gupta, Ashkrit
Pathak, Vaibhav
Mulani, Mohsin
Khan, Salma
Bansal, Tanya
author_sort Fatima, Ambreen
collection PubMed
description Purpose This study aims to describe the magnetic resonance imaging (MRI) of the brain of five patients diagnosed with metronidazole-induced encephalopathy (MIE). In addition, the aim of our study was to better define the topographic distribution of lesions in MIE. Methods We retrospectively evaluated MRI findings before and after drug cessation in five patients diagnosed with MIE at Era’s Lucknow Medical College and Hospital, Lucknow, Uttar Pradesh, India. The main MRI signal changes and lesion locations were studied. Results Among the patients observed, the average age of the patients with MIE was 55 years (range: 30-70 years). Cerebellar dysfunction, mainly ataxia, and altered mental status were seen in the majority of cases. The most frequently involved sites were the dentate nucleus (cerebellum), brain stem, and corpus callosum (splenium). In diffusion-weighted imaging (DWI), most lesions did not show true restricted diffusion, except for a solitary corpus callosum lesion. Conclusion Although drug-related side effects are more common with long-term use of metronidazole, they may also occur with high doses for short durations. The dentate nucleus, the splenium in the corpus callosum, and the brain stem are the most affected structures. Apart from a solitary lesion of the corpus callosum, all identified lesions were reversible at follow-up MRI after discontinuation of metronidazole. The clinical presentation and characteristic MRI changes are highly specific and can be correlated to make a rapid and more accurate diagnosis of this potentially treatable condition. Prognosis is excellent if detected early.
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spelling pubmed-95731272022-10-17 MRI Findings and Topographic Distribution of Lesions in Metronidazole-Induced Encephalopathy Fatima, Ambreen Khanduri, Sachin Sultana, Sadaf ., Surbhi Siddiqui, Saim A Gupta, Ashkrit Pathak, Vaibhav Mulani, Mohsin Khan, Salma Bansal, Tanya Cureus Neurology Purpose This study aims to describe the magnetic resonance imaging (MRI) of the brain of five patients diagnosed with metronidazole-induced encephalopathy (MIE). In addition, the aim of our study was to better define the topographic distribution of lesions in MIE. Methods We retrospectively evaluated MRI findings before and after drug cessation in five patients diagnosed with MIE at Era’s Lucknow Medical College and Hospital, Lucknow, Uttar Pradesh, India. The main MRI signal changes and lesion locations were studied. Results Among the patients observed, the average age of the patients with MIE was 55 years (range: 30-70 years). Cerebellar dysfunction, mainly ataxia, and altered mental status were seen in the majority of cases. The most frequently involved sites were the dentate nucleus (cerebellum), brain stem, and corpus callosum (splenium). In diffusion-weighted imaging (DWI), most lesions did not show true restricted diffusion, except for a solitary corpus callosum lesion. Conclusion Although drug-related side effects are more common with long-term use of metronidazole, they may also occur with high doses for short durations. The dentate nucleus, the splenium in the corpus callosum, and the brain stem are the most affected structures. Apart from a solitary lesion of the corpus callosum, all identified lesions were reversible at follow-up MRI after discontinuation of metronidazole. The clinical presentation and characteristic MRI changes are highly specific and can be correlated to make a rapid and more accurate diagnosis of this potentially treatable condition. Prognosis is excellent if detected early. Cureus 2022-09-14 /pmc/articles/PMC9573127/ /pubmed/36282977 http://dx.doi.org/10.7759/cureus.29145 Text en Copyright © 2022, Fatima et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Neurology
Fatima, Ambreen
Khanduri, Sachin
Sultana, Sadaf
., Surbhi
Siddiqui, Saim A
Gupta, Ashkrit
Pathak, Vaibhav
Mulani, Mohsin
Khan, Salma
Bansal, Tanya
MRI Findings and Topographic Distribution of Lesions in Metronidazole-Induced Encephalopathy
title MRI Findings and Topographic Distribution of Lesions in Metronidazole-Induced Encephalopathy
title_full MRI Findings and Topographic Distribution of Lesions in Metronidazole-Induced Encephalopathy
title_fullStr MRI Findings and Topographic Distribution of Lesions in Metronidazole-Induced Encephalopathy
title_full_unstemmed MRI Findings and Topographic Distribution of Lesions in Metronidazole-Induced Encephalopathy
title_short MRI Findings and Topographic Distribution of Lesions in Metronidazole-Induced Encephalopathy
title_sort mri findings and topographic distribution of lesions in metronidazole-induced encephalopathy
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9573127/
https://www.ncbi.nlm.nih.gov/pubmed/36282977
http://dx.doi.org/10.7759/cureus.29145
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