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COVID‐19‐associated immune‐mediated encephalitis mimicking acute‐onset Creutzfeldt‐Jakob disease
We report a subtype of immune‐mediated encephalitis associated with COVID‐19, which closely mimics acute‐onset sporadic Creutzfeldt–Jakob disease. A 64‐year‐old man presented with confusion, aphasia, myoclonus, and a silent interstitial pneumonia. He tested positive for SARS‐CoV‐2. Cognition and myo...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8670319/ https://www.ncbi.nlm.nih.gov/pubmed/34825771 http://dx.doi.org/10.1002/acn3.51479 |
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author | Beretta, Simone Stabile, Andrea Balducci, Claudia DiFrancesco, Jacopo C. Patruno, Adriana Rona, Roberto Bombino, Michela Capraro, Cristina Andreetta, Francesca Cavalcante, Paola Moda, Fabio Citerio, Giuseppe Foti, Giuseppe Bogliun, Graziella Ferrarese, Carlo |
author_facet | Beretta, Simone Stabile, Andrea Balducci, Claudia DiFrancesco, Jacopo C. Patruno, Adriana Rona, Roberto Bombino, Michela Capraro, Cristina Andreetta, Francesca Cavalcante, Paola Moda, Fabio Citerio, Giuseppe Foti, Giuseppe Bogliun, Graziella Ferrarese, Carlo |
author_sort | Beretta, Simone |
collection | PubMed |
description | We report a subtype of immune‐mediated encephalitis associated with COVID‐19, which closely mimics acute‐onset sporadic Creutzfeldt–Jakob disease. A 64‐year‐old man presented with confusion, aphasia, myoclonus, and a silent interstitial pneumonia. He tested positive for SARS‐CoV‐2. Cognition and myoclonus rapidly deteriorated, EEG evolved to generalized periodic discharges and brain MRI showed multiple cortical DWI hyperintensities. CSF analysis was normal, except for a positive 14‐3‐3 protein. RT‐QuIC analysis was negative. High levels of pro‐inflammatory cytokines were present in the CSF and serum. Treatment with steroids and intravenous immunoglobulins produced EEG and clinical improvement, with a good neurological outcome at a 6‐month follow‐up. |
format | Online Article Text |
id | pubmed-8670319 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86703192021-12-21 COVID‐19‐associated immune‐mediated encephalitis mimicking acute‐onset Creutzfeldt‐Jakob disease Beretta, Simone Stabile, Andrea Balducci, Claudia DiFrancesco, Jacopo C. Patruno, Adriana Rona, Roberto Bombino, Michela Capraro, Cristina Andreetta, Francesca Cavalcante, Paola Moda, Fabio Citerio, Giuseppe Foti, Giuseppe Bogliun, Graziella Ferrarese, Carlo Ann Clin Transl Neurol Case Study We report a subtype of immune‐mediated encephalitis associated with COVID‐19, which closely mimics acute‐onset sporadic Creutzfeldt–Jakob disease. A 64‐year‐old man presented with confusion, aphasia, myoclonus, and a silent interstitial pneumonia. He tested positive for SARS‐CoV‐2. Cognition and myoclonus rapidly deteriorated, EEG evolved to generalized periodic discharges and brain MRI showed multiple cortical DWI hyperintensities. CSF analysis was normal, except for a positive 14‐3‐3 protein. RT‐QuIC analysis was negative. High levels of pro‐inflammatory cytokines were present in the CSF and serum. Treatment with steroids and intravenous immunoglobulins produced EEG and clinical improvement, with a good neurological outcome at a 6‐month follow‐up. John Wiley and Sons Inc. 2021-11-26 /pmc/articles/PMC8670319/ /pubmed/34825771 http://dx.doi.org/10.1002/acn3.51479 Text en © 2021 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Study Beretta, Simone Stabile, Andrea Balducci, Claudia DiFrancesco, Jacopo C. Patruno, Adriana Rona, Roberto Bombino, Michela Capraro, Cristina Andreetta, Francesca Cavalcante, Paola Moda, Fabio Citerio, Giuseppe Foti, Giuseppe Bogliun, Graziella Ferrarese, Carlo COVID‐19‐associated immune‐mediated encephalitis mimicking acute‐onset Creutzfeldt‐Jakob disease |
title | COVID‐19‐associated immune‐mediated encephalitis mimicking acute‐onset Creutzfeldt‐Jakob disease |
title_full | COVID‐19‐associated immune‐mediated encephalitis mimicking acute‐onset Creutzfeldt‐Jakob disease |
title_fullStr | COVID‐19‐associated immune‐mediated encephalitis mimicking acute‐onset Creutzfeldt‐Jakob disease |
title_full_unstemmed | COVID‐19‐associated immune‐mediated encephalitis mimicking acute‐onset Creutzfeldt‐Jakob disease |
title_short | COVID‐19‐associated immune‐mediated encephalitis mimicking acute‐onset Creutzfeldt‐Jakob disease |
title_sort | covid‐19‐associated immune‐mediated encephalitis mimicking acute‐onset creutzfeldt‐jakob disease |
topic | Case Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8670319/ https://www.ncbi.nlm.nih.gov/pubmed/34825771 http://dx.doi.org/10.1002/acn3.51479 |
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