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Creutzfeldt–Jakob Disease: An Unusual Presentation of Corticobasal Syndrome

Corticobasal syndrome is an atypical parkinsonian syndrome consisting of a constellation of clinical findings that can be the result of various etiologies. While most cases are a result of a tauopathy, such as corticobasal degeneration, other etiologies must be considered in the evaluation of patien...

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Autores principales: Gosden, Grant P, Okromelidze, Lela, Sandhu, Sukhwinder Johnny S, Middlebrooks, Erik H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7725196/
https://www.ncbi.nlm.nih.gov/pubmed/33312792
http://dx.doi.org/10.7759/cureus.11393
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author Gosden, Grant P
Okromelidze, Lela
Sandhu, Sukhwinder Johnny S
Middlebrooks, Erik H
author_facet Gosden, Grant P
Okromelidze, Lela
Sandhu, Sukhwinder Johnny S
Middlebrooks, Erik H
author_sort Gosden, Grant P
collection PubMed
description Corticobasal syndrome is an atypical parkinsonian syndrome consisting of a constellation of clinical findings that can be the result of various etiologies. While most cases are a result of a tauopathy, such as corticobasal degeneration, other etiologies must be considered in the evaluation of patients presenting with corticobasal syndrome. We present a case of a patient presenting with clinical features of corticobasal syndrome due to a prion disease, Creutzfeldt-Jakob disease (CJD), who was initially misdiagnosed due to known pitfalls in the CJD diagnostic criteria. We further discuss this unusual manifestation of CJD presenting as corticobasal syndrome and relevant diagnostic consideration in the evaluation of this entity.
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spelling pubmed-77251962020-12-10 Creutzfeldt–Jakob Disease: An Unusual Presentation of Corticobasal Syndrome Gosden, Grant P Okromelidze, Lela Sandhu, Sukhwinder Johnny S Middlebrooks, Erik H Cureus Neurology Corticobasal syndrome is an atypical parkinsonian syndrome consisting of a constellation of clinical findings that can be the result of various etiologies. While most cases are a result of a tauopathy, such as corticobasal degeneration, other etiologies must be considered in the evaluation of patients presenting with corticobasal syndrome. We present a case of a patient presenting with clinical features of corticobasal syndrome due to a prion disease, Creutzfeldt-Jakob disease (CJD), who was initially misdiagnosed due to known pitfalls in the CJD diagnostic criteria. We further discuss this unusual manifestation of CJD presenting as corticobasal syndrome and relevant diagnostic consideration in the evaluation of this entity. Cureus 2020-11-09 /pmc/articles/PMC7725196/ /pubmed/33312792 http://dx.doi.org/10.7759/cureus.11393 Text en Copyright © 2020, Gosden et al. http://creativecommons.org/licenses/by/3.0/ 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 author and source are credited.
spellingShingle Neurology
Gosden, Grant P
Okromelidze, Lela
Sandhu, Sukhwinder Johnny S
Middlebrooks, Erik H
Creutzfeldt–Jakob Disease: An Unusual Presentation of Corticobasal Syndrome
title Creutzfeldt–Jakob Disease: An Unusual Presentation of Corticobasal Syndrome
title_full Creutzfeldt–Jakob Disease: An Unusual Presentation of Corticobasal Syndrome
title_fullStr Creutzfeldt–Jakob Disease: An Unusual Presentation of Corticobasal Syndrome
title_full_unstemmed Creutzfeldt–Jakob Disease: An Unusual Presentation of Corticobasal Syndrome
title_short Creutzfeldt–Jakob Disease: An Unusual Presentation of Corticobasal Syndrome
title_sort creutzfeldt–jakob disease: an unusual presentation of corticobasal syndrome
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7725196/
https://www.ncbi.nlm.nih.gov/pubmed/33312792
http://dx.doi.org/10.7759/cureus.11393
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