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Marchiafava–Bignami Disease Associated with Spinal Involvement

Marchiafava–Bignami disease (MBD) is a rare disorder of unknown etiology, strongly associated with alcoholism and malnutrition. MBD causes primary involvement of the corpus callosum, leading to confusion, dysarthria, seizures, and frequent death. We report the case of a 54-year-old male without a hi...

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Autores principales: Perea, Jhon, Luis, María Belén, Lázaro, Luciana Grimanesa, Scollo, Sergio, Tamargo, Agustina, Crespo, José, Avalle, Maira, Solarz, Horacio, Fernández Liguori, Nora, Alonso, Ricardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7641677/
https://www.ncbi.nlm.nih.gov/pubmed/33194236
http://dx.doi.org/10.1155/2020/8867383
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author Perea, Jhon
Luis, María Belén
Lázaro, Luciana Grimanesa
Scollo, Sergio
Tamargo, Agustina
Crespo, José
Avalle, Maira
Solarz, Horacio
Fernández Liguori, Nora
Alonso, Ricardo
author_facet Perea, Jhon
Luis, María Belén
Lázaro, Luciana Grimanesa
Scollo, Sergio
Tamargo, Agustina
Crespo, José
Avalle, Maira
Solarz, Horacio
Fernández Liguori, Nora
Alonso, Ricardo
author_sort Perea, Jhon
collection PubMed
description Marchiafava–Bignami disease (MBD) is a rare disorder of unknown etiology, strongly associated with alcoholism and malnutrition. MBD causes primary involvement of the corpus callosum, leading to confusion, dysarthria, seizures, and frequent death. We report the case of a 54-year-old male without a history of alcoholism or known malabsorption disease, who presented with altered consciousness and neurologic impairment. Complex B deficiency was addressed. Magnetic resonance imaging (MRI) showed typical corpus callosum lesions. The clinical features and radiologic images suggested spinal cord involvement. Brain histopathologic findings were consistent with MBD. Despite vitamin replacement therapy, he had a poor outcome.
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spelling pubmed-76416772020-11-13 Marchiafava–Bignami Disease Associated with Spinal Involvement Perea, Jhon Luis, María Belén Lázaro, Luciana Grimanesa Scollo, Sergio Tamargo, Agustina Crespo, José Avalle, Maira Solarz, Horacio Fernández Liguori, Nora Alonso, Ricardo Case Rep Neurol Med Case Report Marchiafava–Bignami disease (MBD) is a rare disorder of unknown etiology, strongly associated with alcoholism and malnutrition. MBD causes primary involvement of the corpus callosum, leading to confusion, dysarthria, seizures, and frequent death. We report the case of a 54-year-old male without a history of alcoholism or known malabsorption disease, who presented with altered consciousness and neurologic impairment. Complex B deficiency was addressed. Magnetic resonance imaging (MRI) showed typical corpus callosum lesions. The clinical features and radiologic images suggested spinal cord involvement. Brain histopathologic findings were consistent with MBD. Despite vitamin replacement therapy, he had a poor outcome. Hindawi 2020-10-28 /pmc/articles/PMC7641677/ /pubmed/33194236 http://dx.doi.org/10.1155/2020/8867383 Text en Copyright © 2020 Jhon Perea et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Perea, Jhon
Luis, María Belén
Lázaro, Luciana Grimanesa
Scollo, Sergio
Tamargo, Agustina
Crespo, José
Avalle, Maira
Solarz, Horacio
Fernández Liguori, Nora
Alonso, Ricardo
Marchiafava–Bignami Disease Associated with Spinal Involvement
title Marchiafava–Bignami Disease Associated with Spinal Involvement
title_full Marchiafava–Bignami Disease Associated with Spinal Involvement
title_fullStr Marchiafava–Bignami Disease Associated with Spinal Involvement
title_full_unstemmed Marchiafava–Bignami Disease Associated with Spinal Involvement
title_short Marchiafava–Bignami Disease Associated with Spinal Involvement
title_sort marchiafava–bignami disease associated with spinal involvement
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7641677/
https://www.ncbi.nlm.nih.gov/pubmed/33194236
http://dx.doi.org/10.1155/2020/8867383
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