Rapidly progressive corticobasal degeneration syndrome.

Detalhes bibliográficos
Autor(a) principal: Herrero Valverde, A
Data de Publicação: 2011
Outros Autores: Costa, S, Ginestal, R, Pimentel, J, Timóteo, A
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.10/476
Resumo: Introduction: Corticobasal syndrome (CBS) has a heterogeneous clinical presentation with no specific pathologic substratum. Its accurate diagnosis is a challenge for neurologists; in order to establish CBS definitively, postmortem confirmation is required. Some clinical and radiological features can help to distinguish it from other neurodegenerative conditions, such as Creutzfeldt-Jakob disease (CJD). Clinical Case: A 74-year-old woman presented with language impairment, difficulty in walking and poor attentiveness that had begun 10 days before. Other symptoms, such as asymmetrical extra-pyramidal dysfunction, limb dystonia and ‘alien limb’ phenomena, were established over the next 2 months, with rapid progression. Death occurred 3 months after symptom onset. Laboratory results were normal. Initially, imaging only showed restricted diffusion with bilateral parieto-occipital gyri involvement on DWI-MRI, with unspecific EEG changes. An autopsy was performed. Brain neuropathology confirmed sporadic CJD (sCJD). Conclusions: CBS is a heterogeneous clinical syndrome whose differential diagnosis is extensive. CJD can occasionally present with clinical characteristics resembling CBS. MRI detection of abnormalities in some sequences (FLAIR, DWI), as previously reported, has high diagnostic utility for sCJD diagnosis – especially in early stages – when other tests can still appear normal. Abnormalities on DWI sequencing may not correlate with neuropathological findings, suggesting a functional basis to explain the changes found.
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spelling Rapidly progressive corticobasal degeneration syndrome.Doenças neurodegenerativasDoença de Creutzfeldt-JakobRessonância magnética nuclearCorticobasal degeneration syndromeIntroduction: Corticobasal syndrome (CBS) has a heterogeneous clinical presentation with no specific pathologic substratum. Its accurate diagnosis is a challenge for neurologists; in order to establish CBS definitively, postmortem confirmation is required. Some clinical and radiological features can help to distinguish it from other neurodegenerative conditions, such as Creutzfeldt-Jakob disease (CJD). Clinical Case: A 74-year-old woman presented with language impairment, difficulty in walking and poor attentiveness that had begun 10 days before. Other symptoms, such as asymmetrical extra-pyramidal dysfunction, limb dystonia and ‘alien limb’ phenomena, were established over the next 2 months, with rapid progression. Death occurred 3 months after symptom onset. Laboratory results were normal. Initially, imaging only showed restricted diffusion with bilateral parieto-occipital gyri involvement on DWI-MRI, with unspecific EEG changes. An autopsy was performed. Brain neuropathology confirmed sporadic CJD (sCJD). Conclusions: CBS is a heterogeneous clinical syndrome whose differential diagnosis is extensive. CJD can occasionally present with clinical characteristics resembling CBS. MRI detection of abnormalities in some sequences (FLAIR, DWI), as previously reported, has high diagnostic utility for sCJD diagnosis – especially in early stages – when other tests can still appear normal. Abnormalities on DWI sequencing may not correlate with neuropathological findings, suggesting a functional basis to explain the changes found.KargerRepositório do Hospital Prof. Doutor Fernando FonsecaHerrero Valverde, ACosta, SGinestal, RPimentel, JTimóteo, A2012-02-03T14:28:45Z2011-01-01T00:00:00Z2011-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.10/476engCase Rep Neurol. 2011 May;3(2):185-901662-680Xinfo: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:RCAAP2022-09-20T15:51:23Zoai:repositorio.hff.min-saude.pt:10400.10/476Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T15:51:45.735708Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Rapidly progressive corticobasal degeneration syndrome.
title Rapidly progressive corticobasal degeneration syndrome.
spellingShingle Rapidly progressive corticobasal degeneration syndrome.
Herrero Valverde, A
Doenças neurodegenerativas
Doença de Creutzfeldt-Jakob
Ressonância magnética nuclear
Corticobasal degeneration syndrome
title_short Rapidly progressive corticobasal degeneration syndrome.
title_full Rapidly progressive corticobasal degeneration syndrome.
title_fullStr Rapidly progressive corticobasal degeneration syndrome.
title_full_unstemmed Rapidly progressive corticobasal degeneration syndrome.
title_sort Rapidly progressive corticobasal degeneration syndrome.
author Herrero Valverde, A
author_facet Herrero Valverde, A
Costa, S
Ginestal, R
Pimentel, J
Timóteo, A
author_role author
author2 Costa, S
Ginestal, R
Pimentel, J
Timóteo, A
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Repositório do Hospital Prof. Doutor Fernando Fonseca
dc.contributor.author.fl_str_mv Herrero Valverde, A
Costa, S
Ginestal, R
Pimentel, J
Timóteo, A
dc.subject.por.fl_str_mv Doenças neurodegenerativas
Doença de Creutzfeldt-Jakob
Ressonância magnética nuclear
Corticobasal degeneration syndrome
topic Doenças neurodegenerativas
Doença de Creutzfeldt-Jakob
Ressonância magnética nuclear
Corticobasal degeneration syndrome
description Introduction: Corticobasal syndrome (CBS) has a heterogeneous clinical presentation with no specific pathologic substratum. Its accurate diagnosis is a challenge for neurologists; in order to establish CBS definitively, postmortem confirmation is required. Some clinical and radiological features can help to distinguish it from other neurodegenerative conditions, such as Creutzfeldt-Jakob disease (CJD). Clinical Case: A 74-year-old woman presented with language impairment, difficulty in walking and poor attentiveness that had begun 10 days before. Other symptoms, such as asymmetrical extra-pyramidal dysfunction, limb dystonia and ‘alien limb’ phenomena, were established over the next 2 months, with rapid progression. Death occurred 3 months after symptom onset. Laboratory results were normal. Initially, imaging only showed restricted diffusion with bilateral parieto-occipital gyri involvement on DWI-MRI, with unspecific EEG changes. An autopsy was performed. Brain neuropathology confirmed sporadic CJD (sCJD). Conclusions: CBS is a heterogeneous clinical syndrome whose differential diagnosis is extensive. CJD can occasionally present with clinical characteristics resembling CBS. MRI detection of abnormalities in some sequences (FLAIR, DWI), as previously reported, has high diagnostic utility for sCJD diagnosis – especially in early stages – when other tests can still appear normal. Abnormalities on DWI sequencing may not correlate with neuropathological findings, suggesting a functional basis to explain the changes found.
publishDate 2011
dc.date.none.fl_str_mv 2011-01-01T00:00:00Z
2011-01-01T00:00:00Z
2012-02-03T14:28:45Z
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.10/476
url http://hdl.handle.net/10400.10/476
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Case Rep Neurol. 2011 May;3(2):185-90
1662-680X
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dc.publisher.none.fl_str_mv Karger
publisher.none.fl_str_mv Karger
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