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Multisystem Inflammatory Syndrome in Children Related to SARS-CoV-2
Although data on the incidence and severity of new coronavirus disease 2019 (COVID-19) due to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection showed more significant disease among adults and the elderly, a clinical manifestation characterized by a multisystem inflammatory synd...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7819738/ https://www.ncbi.nlm.nih.gov/pubmed/33479801 http://dx.doi.org/10.1007/s40272-020-00435-x |
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author | Esposito, Susanna Principi, Nicola |
author_facet | Esposito, Susanna Principi, Nicola |
author_sort | Esposito, Susanna |
collection | PubMed |
description | Although data on the incidence and severity of new coronavirus disease 2019 (COVID-19) due to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection showed more significant disease among adults and the elderly, a clinical manifestation characterized by a multisystem inflammatory syndrome was described in children (MIS-C). It was initially thought to be specific to children, but recent reports have shown that it can also occur in adults. MIS-C is characterized by a number of multisystemic manifestations resembling other known previously described illnesses, mainly Kawasaki disease, especially in cases with shock, toxic shock syndrome, and macrophage activation syndrome. Available literature shows that our knowledge of MIS-C is largely incomplete. Its development in strict relation with SARS-CoV-2 infection seems documented and, in most cases, can be considered a post-infectious manifestation secondary to an abnormal immune response for some aspects, similar to that seen in adults several days after SARS-CoV-2 infection. However, in a minority of cases, a clinical picture with symptoms fulfilling criteria for MIS-C diagnosis develops during the acute phase of SARS-CoV-2 infection. It is highly likely that the criteria currently used to diagnose MIS-C are too broad, meaning that children with different diseases are included. As clarity on the pathogenesis of MIS-C is lacking, different therapeutic approaches have been used, but no specific therapy is currently available. Further studies are urgently needed to improve our definition of MIS-C, to define the real impact on child health, and to elucidate the best clinical and therapeutic approach and true prognosis. |
format | Online Article Text |
id | pubmed-7819738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-78197382021-01-22 Multisystem Inflammatory Syndrome in Children Related to SARS-CoV-2 Esposito, Susanna Principi, Nicola Paediatr Drugs Leading Article Although data on the incidence and severity of new coronavirus disease 2019 (COVID-19) due to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection showed more significant disease among adults and the elderly, a clinical manifestation characterized by a multisystem inflammatory syndrome was described in children (MIS-C). It was initially thought to be specific to children, but recent reports have shown that it can also occur in adults. MIS-C is characterized by a number of multisystemic manifestations resembling other known previously described illnesses, mainly Kawasaki disease, especially in cases with shock, toxic shock syndrome, and macrophage activation syndrome. Available literature shows that our knowledge of MIS-C is largely incomplete. Its development in strict relation with SARS-CoV-2 infection seems documented and, in most cases, can be considered a post-infectious manifestation secondary to an abnormal immune response for some aspects, similar to that seen in adults several days after SARS-CoV-2 infection. However, in a minority of cases, a clinical picture with symptoms fulfilling criteria for MIS-C diagnosis develops during the acute phase of SARS-CoV-2 infection. It is highly likely that the criteria currently used to diagnose MIS-C are too broad, meaning that children with different diseases are included. As clarity on the pathogenesis of MIS-C is lacking, different therapeutic approaches have been used, but no specific therapy is currently available. Further studies are urgently needed to improve our definition of MIS-C, to define the real impact on child health, and to elucidate the best clinical and therapeutic approach and true prognosis. Springer International Publishing 2021-01-22 2021 /pmc/articles/PMC7819738/ /pubmed/33479801 http://dx.doi.org/10.1007/s40272-020-00435-x Text en © The Author(s), under exclusive licence to Springer Nature Switzerland AG part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Leading Article Esposito, Susanna Principi, Nicola Multisystem Inflammatory Syndrome in Children Related to SARS-CoV-2 |
title | Multisystem Inflammatory Syndrome in Children Related to SARS-CoV-2 |
title_full | Multisystem Inflammatory Syndrome in Children Related to SARS-CoV-2 |
title_fullStr | Multisystem Inflammatory Syndrome in Children Related to SARS-CoV-2 |
title_full_unstemmed | Multisystem Inflammatory Syndrome in Children Related to SARS-CoV-2 |
title_short | Multisystem Inflammatory Syndrome in Children Related to SARS-CoV-2 |
title_sort | multisystem inflammatory syndrome in children related to sars-cov-2 |
topic | Leading Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7819738/ https://www.ncbi.nlm.nih.gov/pubmed/33479801 http://dx.doi.org/10.1007/s40272-020-00435-x |
work_keys_str_mv | AT espositosusanna multisysteminflammatorysyndromeinchildrenrelatedtosarscov2 AT principinicola multisysteminflammatorysyndromeinchildrenrelatedtosarscov2 |