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Autoimmune myasthenia gravis after COVID-19 in a triple vaccinated patient
Despite a well characterized mechanism, myasthenia gravis (MG) remains a dilemma in terms of etiology. Several case reports and series of cases suggest a potential cause-effect relation between SARS-CoV-2 infection or vaccination and MG. We present the case of an autoimmune MG occurring post Covid-1...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
UMF “Gr. T. Popa” Iasi Publishing House
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9512128/ https://www.ncbi.nlm.nih.gov/pubmed/36176496 http://dx.doi.org/10.22551/2022.36.0903.10212 |
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author | Croitoru, Cristina-Georgiana Cuciureanu, Dan Iulian Prutianu, Iulian Cianga, Petru |
author_facet | Croitoru, Cristina-Georgiana Cuciureanu, Dan Iulian Prutianu, Iulian Cianga, Petru |
author_sort | Croitoru, Cristina-Georgiana |
collection | PubMed |
description | Despite a well characterized mechanism, myasthenia gravis (MG) remains a dilemma in terms of etiology. Several case reports and series of cases suggest a potential cause-effect relation between SARS-CoV-2 infection or vaccination and MG. We present the case of an autoimmune MG occurring post Covid-19 in an elderly male, vaccinated with three doses of the BNT162b2/Pfizer-BioNTech vaccine. The 78-year-old male was admitted in the Neurology Clinic in early November 2021 with double vision, bilateral ptosis, dysphonia and dysphagia, 16 days after receiving a third dose of the BNT162b2/Pfizer-BioNTech SARS-CoV-2 vaccine and 12 days after testing positive for SARS-CoV-2 infection. The symptoms began to emerge at 9 days after COVID-19 diagnosis. Clinical neurological examination included ice-pack test and intramuscular neostigmine, both with positive results. Myasthenia gravis positive diagnosis was confirmed by slow repetitive nerve stimulation and abnormally increased serum levels of antibodies against acetylcholine receptors. Due to patient's refusal of further hospitalization, he was discharged with therapy recommendations. Under treatment with oral pyridostigmine, but no oral corticosteroid due to therapeutic noncompliance, the patient was readmitted two months later with aggravated symptoms. The myasthenic crisis was successfully treated with intravenous immunoglobulins, corticosteroid therapy and oral pyridostigmine. The novelty of the current case resides in the fact that, to the best of our knowledge, appears to be the first case of MG clinically manifested after COVID-19 infection in a fully vaccinated patient. |
format | Online Article Text |
id | pubmed-9512128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | UMF “Gr. T. Popa” Iasi Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-95121282022-09-28 Autoimmune myasthenia gravis after COVID-19 in a triple vaccinated patient Croitoru, Cristina-Georgiana Cuciureanu, Dan Iulian Prutianu, Iulian Cianga, Petru Arch Clin Cases Case Report Despite a well characterized mechanism, myasthenia gravis (MG) remains a dilemma in terms of etiology. Several case reports and series of cases suggest a potential cause-effect relation between SARS-CoV-2 infection or vaccination and MG. We present the case of an autoimmune MG occurring post Covid-19 in an elderly male, vaccinated with three doses of the BNT162b2/Pfizer-BioNTech vaccine. The 78-year-old male was admitted in the Neurology Clinic in early November 2021 with double vision, bilateral ptosis, dysphonia and dysphagia, 16 days after receiving a third dose of the BNT162b2/Pfizer-BioNTech SARS-CoV-2 vaccine and 12 days after testing positive for SARS-CoV-2 infection. The symptoms began to emerge at 9 days after COVID-19 diagnosis. Clinical neurological examination included ice-pack test and intramuscular neostigmine, both with positive results. Myasthenia gravis positive diagnosis was confirmed by slow repetitive nerve stimulation and abnormally increased serum levels of antibodies against acetylcholine receptors. Due to patient's refusal of further hospitalization, he was discharged with therapy recommendations. Under treatment with oral pyridostigmine, but no oral corticosteroid due to therapeutic noncompliance, the patient was readmitted two months later with aggravated symptoms. The myasthenic crisis was successfully treated with intravenous immunoglobulins, corticosteroid therapy and oral pyridostigmine. The novelty of the current case resides in the fact that, to the best of our knowledge, appears to be the first case of MG clinically manifested after COVID-19 infection in a fully vaccinated patient. UMF “Gr. T. Popa” Iasi Publishing House 2022-09-26 /pmc/articles/PMC9512128/ /pubmed/36176496 http://dx.doi.org/10.22551/2022.36.0903.10212 Text en https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Croitoru, Cristina-Georgiana Cuciureanu, Dan Iulian Prutianu, Iulian Cianga, Petru Autoimmune myasthenia gravis after COVID-19 in a triple vaccinated patient |
title | Autoimmune myasthenia gravis after COVID-19 in a triple vaccinated patient |
title_full | Autoimmune myasthenia gravis after COVID-19 in a triple vaccinated patient |
title_fullStr | Autoimmune myasthenia gravis after COVID-19 in a triple vaccinated patient |
title_full_unstemmed | Autoimmune myasthenia gravis after COVID-19 in a triple vaccinated patient |
title_short | Autoimmune myasthenia gravis after COVID-19 in a triple vaccinated patient |
title_sort | autoimmune myasthenia gravis after covid-19 in a triple vaccinated patient |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9512128/ https://www.ncbi.nlm.nih.gov/pubmed/36176496 http://dx.doi.org/10.22551/2022.36.0903.10212 |
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