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A case of COVID-19-associated fulminant myocarditis due to SARS-CoV-2 Omicron BA.2 sub-lineage in an unvaccinated female

COVID-19-associated myocarditis can be a lethal complication in previous variants, but it is not well understood in the Omicron variant. We present an unvaccinated case of COVID-19-associated fulminant myocarditis due to the Omicron BA.2 sub-lineage requiring mechanical circulatory support (MCS). A...

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Autores principales: Ichimura, Shohei, Oikawa, Masayoshi, Ikeda, Ayano, Endo, Keiichiro, Muto, Yuuki, Akama, Joh, Yamaki, Takayoshi, Nakazato, Kazuhiko, Sato, Masahiko, Ishida, Takafumi, Suzuki, Osamu, Takeishi, Yasuchika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese College of Cardiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9946881/
https://www.ncbi.nlm.nih.gov/pubmed/36852014
http://dx.doi.org/10.1016/j.jccase.2023.02.016
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author Ichimura, Shohei
Oikawa, Masayoshi
Ikeda, Ayano
Endo, Keiichiro
Muto, Yuuki
Akama, Joh
Yamaki, Takayoshi
Nakazato, Kazuhiko
Sato, Masahiko
Ishida, Takafumi
Suzuki, Osamu
Takeishi, Yasuchika
author_facet Ichimura, Shohei
Oikawa, Masayoshi
Ikeda, Ayano
Endo, Keiichiro
Muto, Yuuki
Akama, Joh
Yamaki, Takayoshi
Nakazato, Kazuhiko
Sato, Masahiko
Ishida, Takafumi
Suzuki, Osamu
Takeishi, Yasuchika
author_sort Ichimura, Shohei
collection PubMed
description COVID-19-associated myocarditis can be a lethal complication in previous variants, but it is not well understood in the Omicron variant. We present an unvaccinated case of COVID-19-associated fulminant myocarditis due to the Omicron BA.2 sub-lineage requiring mechanical circulatory support (MCS). A 66-year-old female without vaccination against SARS-CoV-2 was hospitalized due to COVID-19. On the next day, she was transferred to our hospital due to the development of fulminant myocarditis. After arrival, she was treated with Impella CP and venoarterial extracorporeal membrane oxygenation due to unstable hemodynamics. In addition to MCS, we treated her with inotropes, methylprednisolone, tocilizumab, and remdesivir. Left ventricular contraction gradually improved, and MCS was removed on day 8. Endomyocardial biopsy showed mild interstitial infiltration of CD3(+)-T lymphocytes and CD68(+)-macrophages with no remarkable necrosis or fibrosis. This case showed similar histological characteristics to COVID-19-associated myocarditis before the Omicron variant. The vaccination against the Omicron variant should be considered to prevent the development of severe illness, including fulminant myocarditis. LEARNING OBJECTIVE: Although the Omicron variant is thought to be generally less severe, COVID-19-associated fulminant myocarditis, as in this case, can occur. The vaccination against the Omicron variant should be considered to prevent from developing severe illness.
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spelling pubmed-99468812023-02-23 A case of COVID-19-associated fulminant myocarditis due to SARS-CoV-2 Omicron BA.2 sub-lineage in an unvaccinated female Ichimura, Shohei Oikawa, Masayoshi Ikeda, Ayano Endo, Keiichiro Muto, Yuuki Akama, Joh Yamaki, Takayoshi Nakazato, Kazuhiko Sato, Masahiko Ishida, Takafumi Suzuki, Osamu Takeishi, Yasuchika J Cardiol Cases Case Report COVID-19-associated myocarditis can be a lethal complication in previous variants, but it is not well understood in the Omicron variant. We present an unvaccinated case of COVID-19-associated fulminant myocarditis due to the Omicron BA.2 sub-lineage requiring mechanical circulatory support (MCS). A 66-year-old female without vaccination against SARS-CoV-2 was hospitalized due to COVID-19. On the next day, she was transferred to our hospital due to the development of fulminant myocarditis. After arrival, she was treated with Impella CP and venoarterial extracorporeal membrane oxygenation due to unstable hemodynamics. In addition to MCS, we treated her with inotropes, methylprednisolone, tocilizumab, and remdesivir. Left ventricular contraction gradually improved, and MCS was removed on day 8. Endomyocardial biopsy showed mild interstitial infiltration of CD3(+)-T lymphocytes and CD68(+)-macrophages with no remarkable necrosis or fibrosis. This case showed similar histological characteristics to COVID-19-associated myocarditis before the Omicron variant. The vaccination against the Omicron variant should be considered to prevent the development of severe illness, including fulminant myocarditis. LEARNING OBJECTIVE: Although the Omicron variant is thought to be generally less severe, COVID-19-associated fulminant myocarditis, as in this case, can occur. The vaccination against the Omicron variant should be considered to prevent from developing severe illness. Japanese College of Cardiology 2023-02-23 /pmc/articles/PMC9946881/ /pubmed/36852014 http://dx.doi.org/10.1016/j.jccase.2023.02.016 Text en © 2023 Japanese College of Cardiology. Published by Elsevier Ltd. All rights reserved.
spellingShingle Case Report
Ichimura, Shohei
Oikawa, Masayoshi
Ikeda, Ayano
Endo, Keiichiro
Muto, Yuuki
Akama, Joh
Yamaki, Takayoshi
Nakazato, Kazuhiko
Sato, Masahiko
Ishida, Takafumi
Suzuki, Osamu
Takeishi, Yasuchika
A case of COVID-19-associated fulminant myocarditis due to SARS-CoV-2 Omicron BA.2 sub-lineage in an unvaccinated female
title A case of COVID-19-associated fulminant myocarditis due to SARS-CoV-2 Omicron BA.2 sub-lineage in an unvaccinated female
title_full A case of COVID-19-associated fulminant myocarditis due to SARS-CoV-2 Omicron BA.2 sub-lineage in an unvaccinated female
title_fullStr A case of COVID-19-associated fulminant myocarditis due to SARS-CoV-2 Omicron BA.2 sub-lineage in an unvaccinated female
title_full_unstemmed A case of COVID-19-associated fulminant myocarditis due to SARS-CoV-2 Omicron BA.2 sub-lineage in an unvaccinated female
title_short A case of COVID-19-associated fulminant myocarditis due to SARS-CoV-2 Omicron BA.2 sub-lineage in an unvaccinated female
title_sort case of covid-19-associated fulminant myocarditis due to sars-cov-2 omicron ba.2 sub-lineage in an unvaccinated female
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9946881/
https://www.ncbi.nlm.nih.gov/pubmed/36852014
http://dx.doi.org/10.1016/j.jccase.2023.02.016
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