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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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Detalles Bibliográficos
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
Descripción
Sumario: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.