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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2020
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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. |
format | Online Article Text |
id | pubmed-7725196 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
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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