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Case Report: A case of multisystem inflammatory syndrome in an 11-year-old female after COVID-19 inactivated vaccine

BACKGROUND: Multisystem inflammatory syndrome in children (MIS-C), also known as pediatric inflammatory, multisystem syndrome temporally associated with SARS-CoV-2, is a rare but serious complication of SARS-CoV-2 infection in children that typically occurs 2–6 weeks after SARS-CoV-2 infection. The...

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Autores principales: Saeed, Saboor, Cao, Jianqing, Xu, Jinjiao, Zhang, Yi, Zheng, Xuyang, Jiang, Liya, Jiang, Chunming, Zhang, Xinjuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9972091/
https://www.ncbi.nlm.nih.gov/pubmed/36865693
http://dx.doi.org/10.3389/fped.2023.1068301
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author Saeed, Saboor
Cao, Jianqing
Xu, Jinjiao
Zhang, Yi
Zheng, Xuyang
Jiang, Liya
Jiang, Chunming
Zhang, Xinjuan
author_facet Saeed, Saboor
Cao, Jianqing
Xu, Jinjiao
Zhang, Yi
Zheng, Xuyang
Jiang, Liya
Jiang, Chunming
Zhang, Xinjuan
author_sort Saeed, Saboor
collection PubMed
description BACKGROUND: Multisystem inflammatory syndrome in children (MIS-C), also known as pediatric inflammatory, multisystem syndrome temporally associated with SARS-CoV-2, is a rare but serious complication of SARS-CoV-2 infection in children that typically occurs 2–6 weeks after SARS-CoV-2 infection. The pathophysiology of MIS-C is unknown. MIS-C, first recognized in April 2020, is characterized by fever, systemic inflammation, and multi-system organ involvement. Post-vaccination adverse effects have increased with COVID-19 vaccinations, and MIS linked to immunization with COVID-19 vaccines has also been observed. CASE REPORT: An 11-year-old Chinese girl presented with a high-grade fever, rash, and dry cough for 2 days. She had her 2nd SARS-CoV-2 inactivated vaccination dose five days before hospital admission. On day 3 & 4, she experienced bilateral conjunctivitis, hypotension (66/47 mmHg), and a high CRP level. She was diagnosed with MIS-C. The patient's condition deteriorated rapidly, necessitating intensive care unit admission. The patient's symptoms improved after intravenous immunoglobulin, methylprednisolone, and oral aspirin therapy. She was discharged from the hospital after 16 days as her general condition, and laboratory biomarkers returned to normal. CONCLUSION: Inactivated Covid-19 vaccination might trigger MIS-C. Further research is needed to evaluate whether a correlation exists between COVID-19 vaccination and MIS-C development.
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spelling pubmed-99720912023-03-01 Case Report: A case of multisystem inflammatory syndrome in an 11-year-old female after COVID-19 inactivated vaccine Saeed, Saboor Cao, Jianqing Xu, Jinjiao Zhang, Yi Zheng, Xuyang Jiang, Liya Jiang, Chunming Zhang, Xinjuan Front Pediatr Pediatrics BACKGROUND: Multisystem inflammatory syndrome in children (MIS-C), also known as pediatric inflammatory, multisystem syndrome temporally associated with SARS-CoV-2, is a rare but serious complication of SARS-CoV-2 infection in children that typically occurs 2–6 weeks after SARS-CoV-2 infection. The pathophysiology of MIS-C is unknown. MIS-C, first recognized in April 2020, is characterized by fever, systemic inflammation, and multi-system organ involvement. Post-vaccination adverse effects have increased with COVID-19 vaccinations, and MIS linked to immunization with COVID-19 vaccines has also been observed. CASE REPORT: An 11-year-old Chinese girl presented with a high-grade fever, rash, and dry cough for 2 days. She had her 2nd SARS-CoV-2 inactivated vaccination dose five days before hospital admission. On day 3 & 4, she experienced bilateral conjunctivitis, hypotension (66/47 mmHg), and a high CRP level. She was diagnosed with MIS-C. The patient's condition deteriorated rapidly, necessitating intensive care unit admission. The patient's symptoms improved after intravenous immunoglobulin, methylprednisolone, and oral aspirin therapy. She was discharged from the hospital after 16 days as her general condition, and laboratory biomarkers returned to normal. CONCLUSION: Inactivated Covid-19 vaccination might trigger MIS-C. Further research is needed to evaluate whether a correlation exists between COVID-19 vaccination and MIS-C development. Frontiers Media S.A. 2023-02-14 /pmc/articles/PMC9972091/ /pubmed/36865693 http://dx.doi.org/10.3389/fped.2023.1068301 Text en © 2023 Saeed, Cao, Xu, Zhang, Zheng, Jiang, Jiang and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Saeed, Saboor
Cao, Jianqing
Xu, Jinjiao
Zhang, Yi
Zheng, Xuyang
Jiang, Liya
Jiang, Chunming
Zhang, Xinjuan
Case Report: A case of multisystem inflammatory syndrome in an 11-year-old female after COVID-19 inactivated vaccine
title Case Report: A case of multisystem inflammatory syndrome in an 11-year-old female after COVID-19 inactivated vaccine
title_full Case Report: A case of multisystem inflammatory syndrome in an 11-year-old female after COVID-19 inactivated vaccine
title_fullStr Case Report: A case of multisystem inflammatory syndrome in an 11-year-old female after COVID-19 inactivated vaccine
title_full_unstemmed Case Report: A case of multisystem inflammatory syndrome in an 11-year-old female after COVID-19 inactivated vaccine
title_short Case Report: A case of multisystem inflammatory syndrome in an 11-year-old female after COVID-19 inactivated vaccine
title_sort case report: a case of multisystem inflammatory syndrome in an 11-year-old female after covid-19 inactivated vaccine
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9972091/
https://www.ncbi.nlm.nih.gov/pubmed/36865693
http://dx.doi.org/10.3389/fped.2023.1068301
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