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Apport de l'IRM dans la maladie de Creutzfeldt-Jakob: à propos d'un cas

Creutzfeldt-jakob disease (CJD) is a very rare and fatal disease affecting the central nervous system. It is characterized by mental deterioration leading to progressive dementia, pyramidal and extrapyramidal symptoms as well as myoclonus. Early diagnosis is essential to prevent human-to-human trans...

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Autores principales: Alaoui, Amina, Alami, Badraddine, Habibi, Hajar, Haloua, Meriem, Lamrani, Youssef Alaoui, Boubbou, Meryem, Maaroufi, Mustapha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6560989/
https://www.ncbi.nlm.nih.gov/pubmed/31223386
http://dx.doi.org/10.11604/pamj.2019.32.95.17819
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author Alaoui, Amina
Alami, Badraddine
Habibi, Hajar
Haloua, Meriem
Lamrani, Youssef Alaoui
Boubbou, Meryem
Maaroufi, Mustapha
author_facet Alaoui, Amina
Alami, Badraddine
Habibi, Hajar
Haloua, Meriem
Lamrani, Youssef Alaoui
Boubbou, Meryem
Maaroufi, Mustapha
author_sort Alaoui, Amina
collection PubMed
description Creutzfeldt-jakob disease (CJD) is a very rare and fatal disease affecting the central nervous system. It is characterized by mental deterioration leading to progressive dementia, pyramidal and extrapyramidal symptoms as well as myoclonus. Early diagnosis is essential to prevent human-to-human transmission. We here report the case of a 62-year old patient in whom the diagnosis of sporadic CJD was retained based on his clinical status including dementia-related deterioration with myoclonus preceded by behavioral disorders, hallucinations and depression and on brain MRI data showing hyperintensities at the level of the striatum and the cortex on FLAIR and diffusion-weighted imaging sequences.
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spelling pubmed-65609892019-06-20 Apport de l'IRM dans la maladie de Creutzfeldt-Jakob: à propos d'un cas Alaoui, Amina Alami, Badraddine Habibi, Hajar Haloua, Meriem Lamrani, Youssef Alaoui Boubbou, Meryem Maaroufi, Mustapha Pan Afr Med J Case Report Creutzfeldt-jakob disease (CJD) is a very rare and fatal disease affecting the central nervous system. It is characterized by mental deterioration leading to progressive dementia, pyramidal and extrapyramidal symptoms as well as myoclonus. Early diagnosis is essential to prevent human-to-human transmission. We here report the case of a 62-year old patient in whom the diagnosis of sporadic CJD was retained based on his clinical status including dementia-related deterioration with myoclonus preceded by behavioral disorders, hallucinations and depression and on brain MRI data showing hyperintensities at the level of the striatum and the cortex on FLAIR and diffusion-weighted imaging sequences. The African Field Epidemiology Network 2019-02-28 /pmc/articles/PMC6560989/ /pubmed/31223386 http://dx.doi.org/10.11604/pamj.2019.32.95.17819 Text en © Amina Alaoui et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. 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 work is properly cited.
spellingShingle Case Report
Alaoui, Amina
Alami, Badraddine
Habibi, Hajar
Haloua, Meriem
Lamrani, Youssef Alaoui
Boubbou, Meryem
Maaroufi, Mustapha
Apport de l'IRM dans la maladie de Creutzfeldt-Jakob: à propos d'un cas
title Apport de l'IRM dans la maladie de Creutzfeldt-Jakob: à propos d'un cas
title_full Apport de l'IRM dans la maladie de Creutzfeldt-Jakob: à propos d'un cas
title_fullStr Apport de l'IRM dans la maladie de Creutzfeldt-Jakob: à propos d'un cas
title_full_unstemmed Apport de l'IRM dans la maladie de Creutzfeldt-Jakob: à propos d'un cas
title_short Apport de l'IRM dans la maladie de Creutzfeldt-Jakob: à propos d'un cas
title_sort apport de l'irm dans la maladie de creutzfeldt-jakob: à propos d'un cas
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6560989/
https://www.ncbi.nlm.nih.gov/pubmed/31223386
http://dx.doi.org/10.11604/pamj.2019.32.95.17819
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