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Cardiogenic shock complicating multisystem inflammatory syndrome following COVID-19 infection: a case report
BACKGROUND: With the high prevalence of COVID-19 infections worldwide, the multisystem inflammatory syndrome in adults (MIS-A) is becoming an increasingly recognized entity. This syndrome presents in patients several weeks after infection with COVID-19 and is associated with thrombosis, elevated inf...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8555861/ https://www.ncbi.nlm.nih.gov/pubmed/34715788 http://dx.doi.org/10.1186/s12872-021-02304-y |
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author | Gurin, Michael I. Lin, Yue J. Bernard, Samuel Goldberg, Randal I. Narula, Navneet Faillace, Robert T. Alviar, Carlos L. Bangalore, Sripal Keller, Norma M. |
author_facet | Gurin, Michael I. Lin, Yue J. Bernard, Samuel Goldberg, Randal I. Narula, Navneet Faillace, Robert T. Alviar, Carlos L. Bangalore, Sripal Keller, Norma M. |
author_sort | Gurin, Michael I. |
collection | PubMed |
description | BACKGROUND: With the high prevalence of COVID-19 infections worldwide, the multisystem inflammatory syndrome in adults (MIS-A) is becoming an increasingly recognized entity. This syndrome presents in patients several weeks after infection with COVID-19 and is associated with thrombosis, elevated inflammatory markers, hemodynamic compromise and cardiac dysfunction. Treatment is often with steroids and intravenous immunoglobulin (IVIg). The pathologic basis of myocardial injury in MIS-A, however, is not well characterized. In our case report, we obtained endomyocardial biopsy that revealed a pattern of myocardial injury similar to that found in COVID-19 cardiac specimens. CASE PRESENTATION: A 26-year-old male presented with fevers, chills, headache, nausea, vomiting, and diarrhea 5 weeks after his COVID-19 infection. His SARS-CoV-2 PCR was negative and IgG was positive, consistent with prior infection. He was found to be in cardiogenic shock with biventricular failure, requiring inotropes and diuretics. Given concern for acute fulminant myocarditis, an endomyocardial biopsy (EMB) was performed, showing an inflammatory infiltrate consisting predominantly of interstitial macrophages with scant T lymphocytes. The histologic pattern was similar to that of cardiac specimens from COVID-19 patients, helping rule out myocarditis as the prevailing diagnosis. His case was complicated by persistent hypoxemia, and a computed tomography scan revealed pulmonary emboli. He received IVIg, steroids, and anticoagulation with rapid recovery of biventricular function. CONCLUSIONS: MIS-A should be considered as the diagnosis in patients presenting several weeks after COVID-19 infection with severe inflammation and multi-organ involvement. In our case, EMB facilitated identification of MIS-A and guided therapy. The patient’s biventricular function recovered with IVIg and steroids. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12872-021-02304-y. |
format | Online Article Text |
id | pubmed-8555861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85558612021-11-01 Cardiogenic shock complicating multisystem inflammatory syndrome following COVID-19 infection: a case report Gurin, Michael I. Lin, Yue J. Bernard, Samuel Goldberg, Randal I. Narula, Navneet Faillace, Robert T. Alviar, Carlos L. Bangalore, Sripal Keller, Norma M. BMC Cardiovasc Disord Case Report BACKGROUND: With the high prevalence of COVID-19 infections worldwide, the multisystem inflammatory syndrome in adults (MIS-A) is becoming an increasingly recognized entity. This syndrome presents in patients several weeks after infection with COVID-19 and is associated with thrombosis, elevated inflammatory markers, hemodynamic compromise and cardiac dysfunction. Treatment is often with steroids and intravenous immunoglobulin (IVIg). The pathologic basis of myocardial injury in MIS-A, however, is not well characterized. In our case report, we obtained endomyocardial biopsy that revealed a pattern of myocardial injury similar to that found in COVID-19 cardiac specimens. CASE PRESENTATION: A 26-year-old male presented with fevers, chills, headache, nausea, vomiting, and diarrhea 5 weeks after his COVID-19 infection. His SARS-CoV-2 PCR was negative and IgG was positive, consistent with prior infection. He was found to be in cardiogenic shock with biventricular failure, requiring inotropes and diuretics. Given concern for acute fulminant myocarditis, an endomyocardial biopsy (EMB) was performed, showing an inflammatory infiltrate consisting predominantly of interstitial macrophages with scant T lymphocytes. The histologic pattern was similar to that of cardiac specimens from COVID-19 patients, helping rule out myocarditis as the prevailing diagnosis. His case was complicated by persistent hypoxemia, and a computed tomography scan revealed pulmonary emboli. He received IVIg, steroids, and anticoagulation with rapid recovery of biventricular function. CONCLUSIONS: MIS-A should be considered as the diagnosis in patients presenting several weeks after COVID-19 infection with severe inflammation and multi-organ involvement. In our case, EMB facilitated identification of MIS-A and guided therapy. The patient’s biventricular function recovered with IVIg and steroids. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12872-021-02304-y. BioMed Central 2021-10-29 /pmc/articles/PMC8555861/ /pubmed/34715788 http://dx.doi.org/10.1186/s12872-021-02304-y 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 Gurin, Michael I. Lin, Yue J. Bernard, Samuel Goldberg, Randal I. Narula, Navneet Faillace, Robert T. Alviar, Carlos L. Bangalore, Sripal Keller, Norma M. Cardiogenic shock complicating multisystem inflammatory syndrome following COVID-19 infection: a case report |
title | Cardiogenic shock complicating multisystem inflammatory syndrome following COVID-19 infection: a case report |
title_full | Cardiogenic shock complicating multisystem inflammatory syndrome following COVID-19 infection: a case report |
title_fullStr | Cardiogenic shock complicating multisystem inflammatory syndrome following COVID-19 infection: a case report |
title_full_unstemmed | Cardiogenic shock complicating multisystem inflammatory syndrome following COVID-19 infection: a case report |
title_short | Cardiogenic shock complicating multisystem inflammatory syndrome following COVID-19 infection: a case report |
title_sort | cardiogenic shock complicating multisystem inflammatory syndrome following covid-19 infection: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8555861/ https://www.ncbi.nlm.nih.gov/pubmed/34715788 http://dx.doi.org/10.1186/s12872-021-02304-y |
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