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Miller Fisher syndrome following BNT162b2 mRNA coronavirus 2019 vaccination
BACKGROUND: The coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), began in late 2019. One of the vaccines approved against COVID-19 is the BNT162b2 mRNA COVID-19 vaccine (Pfizer/BioNTech). CASE PRESENTATION: We present the case of a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8598937/ https://www.ncbi.nlm.nih.gov/pubmed/34789193 http://dx.doi.org/10.1186/s12883-021-02489-x |
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author | Nishiguchi, Yamato Matsuyama, Hirofumi Maeda, Kuniko Shindo, Akihiro Tomimoto, Hidekazu |
author_facet | Nishiguchi, Yamato Matsuyama, Hirofumi Maeda, Kuniko Shindo, Akihiro Tomimoto, Hidekazu |
author_sort | Nishiguchi, Yamato |
collection | PubMed |
description | BACKGROUND: The coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), began in late 2019. One of the vaccines approved against COVID-19 is the BNT162b2 mRNA COVID-19 vaccine (Pfizer/BioNTech). CASE PRESENTATION: We present the case of a 71-year-old man with no history of the SARS-CoV-2 infection or any recent viral or bacterial illnesses who presented with bilateral oculomotor palsy and limb ataxia after BNT162b2 mRNA COVID-19 vaccination. The diagnosis of Miller Fisher syndrome (MFS) was established based on physical examination, brain magnetic resonance imaging (MRI), cerebrospinal fluid analysis (CSF), and positron emission tomography (PET). There was no evidence of other predisposing infectious or autoimmune factors, and the period from COVID-19 vaccination to the appearance of neurological symptoms was similar to that of other vaccines and preceding events, such as infection. CONCLUSION: Guillain–Barré syndrome (GBS) and its variants after COVID-19 vaccination are extremely rare. Note that more research is needed to establish an association between MFS and COVID-19 vaccines. In our opinion, the benefits of COVID-19 vaccination largely outweigh its risks. |
format | Online Article Text |
id | pubmed-8598937 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85989372021-11-18 Miller Fisher syndrome following BNT162b2 mRNA coronavirus 2019 vaccination Nishiguchi, Yamato Matsuyama, Hirofumi Maeda, Kuniko Shindo, Akihiro Tomimoto, Hidekazu BMC Neurol Case Report BACKGROUND: The coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), began in late 2019. One of the vaccines approved against COVID-19 is the BNT162b2 mRNA COVID-19 vaccine (Pfizer/BioNTech). CASE PRESENTATION: We present the case of a 71-year-old man with no history of the SARS-CoV-2 infection or any recent viral or bacterial illnesses who presented with bilateral oculomotor palsy and limb ataxia after BNT162b2 mRNA COVID-19 vaccination. The diagnosis of Miller Fisher syndrome (MFS) was established based on physical examination, brain magnetic resonance imaging (MRI), cerebrospinal fluid analysis (CSF), and positron emission tomography (PET). There was no evidence of other predisposing infectious or autoimmune factors, and the period from COVID-19 vaccination to the appearance of neurological symptoms was similar to that of other vaccines and preceding events, such as infection. CONCLUSION: Guillain–Barré syndrome (GBS) and its variants after COVID-19 vaccination are extremely rare. Note that more research is needed to establish an association between MFS and COVID-19 vaccines. In our opinion, the benefits of COVID-19 vaccination largely outweigh its risks. BioMed Central 2021-11-18 /pmc/articles/PMC8598937/ /pubmed/34789193 http://dx.doi.org/10.1186/s12883-021-02489-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Nishiguchi, Yamato Matsuyama, Hirofumi Maeda, Kuniko Shindo, Akihiro Tomimoto, Hidekazu Miller Fisher syndrome following BNT162b2 mRNA coronavirus 2019 vaccination |
title | Miller Fisher syndrome following BNT162b2 mRNA coronavirus 2019 vaccination |
title_full | Miller Fisher syndrome following BNT162b2 mRNA coronavirus 2019 vaccination |
title_fullStr | Miller Fisher syndrome following BNT162b2 mRNA coronavirus 2019 vaccination |
title_full_unstemmed | Miller Fisher syndrome following BNT162b2 mRNA coronavirus 2019 vaccination |
title_short | Miller Fisher syndrome following BNT162b2 mRNA coronavirus 2019 vaccination |
title_sort | miller fisher syndrome following bnt162b2 mrna coronavirus 2019 vaccination |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8598937/ https://www.ncbi.nlm.nih.gov/pubmed/34789193 http://dx.doi.org/10.1186/s12883-021-02489-x |
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