ARP Case Report nº 28: What is your diagnosis?

Detalhes bibliográficos
Autor(a) principal: Oliveira, Tiago
Data de Publicação: 2023
Outros Autores: Ferreira, Luís Amaral, Oliveira, Carlos, Donato, Paulo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.25748/arp.30647
Resumo: A 78-year-old female patient was admitted to the emergency department of our institution with a history of psychomotor retardation, myoclonus and dysarthria, over the last 2 months. Her past medical history only included atrial fibrillation with a rapid ventricular response. The neurological examination confirmed the findings mentioned above and an electroencephalography was performed which showed the presence of encephalopathy. The patient was admitted with a presumptive diagnosis of transmissible spongiform encephalopathy (Creutzfeldt-Jakob disease). A cerebral MRI (not shown) was conducted, which not only excluded this diagnosis but also revealed the presence of areas of hyperintense signal on T1-weighted images with ill-defined margins, symmetrically affecting the globus pallidus and the medial region of the cerebral peduncles’ feet. These findings were compatible with liver encephalopathy. Computed Tomography (CT) of the abdomen and Digital Subtraction Venography (DSV) were performed for further investigation. What is your diagnosis?
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spelling ARP Case Report nº 28: What is your diagnosis?ARP Case Report nº 28: What is your diagnosis?Casos ARPA 78-year-old female patient was admitted to the emergency department of our institution with a history of psychomotor retardation, myoclonus and dysarthria, over the last 2 months. Her past medical history only included atrial fibrillation with a rapid ventricular response. The neurological examination confirmed the findings mentioned above and an electroencephalography was performed which showed the presence of encephalopathy. The patient was admitted with a presumptive diagnosis of transmissible spongiform encephalopathy (Creutzfeldt-Jakob disease). A cerebral MRI (not shown) was conducted, which not only excluded this diagnosis but also revealed the presence of areas of hyperintense signal on T1-weighted images with ill-defined margins, symmetrically affecting the globus pallidus and the medial region of the cerebral peduncles’ feet. These findings were compatible with liver encephalopathy. Computed Tomography (CT) of the abdomen and Digital Subtraction Venography (DSV) were performed for further investigation. What is your diagnosis?SPRMN2023-04-30info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://doi.org/10.25748/arp.30647eng2183-13512183-1351Oliveira, TiagoFerreira, Luís AmaralOliveira, CarlosDonato, Pauloinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-05-05T03:15:37ZPortal AgregadorONG
dc.title.none.fl_str_mv ARP Case Report nº 28: What is your diagnosis?
ARP Case Report nº 28: What is your diagnosis?
title ARP Case Report nº 28: What is your diagnosis?
spellingShingle ARP Case Report nº 28: What is your diagnosis?
Oliveira, Tiago
Casos ARP
title_short ARP Case Report nº 28: What is your diagnosis?
title_full ARP Case Report nº 28: What is your diagnosis?
title_fullStr ARP Case Report nº 28: What is your diagnosis?
title_full_unstemmed ARP Case Report nº 28: What is your diagnosis?
title_sort ARP Case Report nº 28: What is your diagnosis?
author Oliveira, Tiago
author_facet Oliveira, Tiago
Ferreira, Luís Amaral
Oliveira, Carlos
Donato, Paulo
author_role author
author2 Ferreira, Luís Amaral
Oliveira, Carlos
Donato, Paulo
author2_role author
author
author
dc.contributor.author.fl_str_mv Oliveira, Tiago
Ferreira, Luís Amaral
Oliveira, Carlos
Donato, Paulo
dc.subject.por.fl_str_mv Casos ARP
topic Casos ARP
description A 78-year-old female patient was admitted to the emergency department of our institution with a history of psychomotor retardation, myoclonus and dysarthria, over the last 2 months. Her past medical history only included atrial fibrillation with a rapid ventricular response. The neurological examination confirmed the findings mentioned above and an electroencephalography was performed which showed the presence of encephalopathy. The patient was admitted with a presumptive diagnosis of transmissible spongiform encephalopathy (Creutzfeldt-Jakob disease). A cerebral MRI (not shown) was conducted, which not only excluded this diagnosis but also revealed the presence of areas of hyperintense signal on T1-weighted images with ill-defined margins, symmetrically affecting the globus pallidus and the medial region of the cerebral peduncles’ feet. These findings were compatible with liver encephalopathy. Computed Tomography (CT) of the abdomen and Digital Subtraction Venography (DSV) were performed for further investigation. What is your diagnosis?
publishDate 2023
dc.date.none.fl_str_mv 2023-04-30
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv https://doi.org/10.25748/arp.30647
url https://doi.org/10.25748/arp.30647
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 2183-1351
2183-1351
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eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv SPRMN
publisher.none.fl_str_mv SPRMN
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