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Multisystem inflammatory syndrome in children and Kawasaki disease: a critical comparison.
Sharma, Chetan; Ganigara, Madhusudan; Galeotti, Caroline; Burns, Joseph; Berganza, Fernando M; Hayes, Denise A; Singh-Grewal, Davinder; Bharath, Suman; Sajjan, Sujata; Bayry, Jagadeesh.
  • Sharma C; Division of Paediatric Cardiology, Children's Hospital of San Antonio/Baylor College of Medicine, San Antonio, TX, USA. Chetan.Sharma@bcm.edu.
  • Ganigara M; Division of Paediatric Cardiology, The University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Galeotti C; Service de Rhumatologie Pédiatrique, Centre de Référence des Maladies Auto-Inflammatoires Rares et des Amyloses, CHU de Bicêtre, le Kremlin Bicêtre, France.
  • Burns J; Division of Paediatrics, Cohen Children's Medical Center, New Hyde Park, NY, USA.
  • Berganza FM; Division of Paediatric Cardiology, Driscoll Children's Hospital, Driscoll, TX, USA.
  • Hayes DA; Division of Paediatric Cardiology, Cohen Children's Medical Center, New Hyde Park, NY, USA.
  • Singh-Grewal D; Division of Paediatric Rheumatology, The Sydney Children's Hospitals Network, Sydney, NSW, Australia.
  • Bharath S; Division of Neurology, John F Kennedy Medical Center/Hackensack Meridian University, Edison, NJ, USA.
  • Sajjan S; Division of Pathology and Laboratory Medicine, Northwell Health Laboratories, Lake Success, NY, USA.
  • Bayry J; Institut National de la Santé et de la Recherche Médicale, Centre de Recherche des Cordeliers, Sorbonne Université, Université de Paris, Paris, France. bayry@iitpkd.ac.in.
Nat Rev Rheumatol ; 17(12): 731-748, 2021 12.
Article in English | MEDLINE | ID: covidwho-1493129
ABSTRACT
Children and adolescents infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are predominantly asymptomatic or have mild symptoms compared with the more severe coronavirus disease 2019 (COVID-19) described in adults. However, SARS-CoV-2 is also associated with a widely reported but poorly understood paediatric systemic vasculitis. This multisystem inflammatory syndrome in children (MIS-C) has features that overlap with myocarditis, toxic-shock syndrome and Kawasaki disease. Current evidence indicates that MIS-C is the result of an exaggerated innate and adaptive immune response, characterized by a cytokine storm, and that it is triggered by prior SARS-CoV-2 exposure. Epidemiological, clinical and immunological differences classify MIS-C as being distinct from Kawasaki disease. Differences include the age range, and the geographical and ethnic distribution of patients. MIS-C is associated with prominent gastrointestinal and cardiovascular system involvement, admission to intensive care unit, neutrophilia, lymphopenia, high levels of IFNγ and low counts of naive CD4+ T cells, with a high proportion of activated memory T cells. Further investigation of MIS-C will continue to enhance our understanding of similar conditions associated with a cytokine storm.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Systemic Inflammatory Response Syndrome / COVID-19 / Mucocutaneous Lymph Node Syndrome Type of study: Observational study / Prognostic study Topics: Long Covid Limits: Adolescent / Child / Humans Language: English Journal: Nat Rev Rheumatol Journal subject: Rheumatology Year: 2021 Document Type: Article Affiliation country: S41584-021-00709-9

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Systemic Inflammatory Response Syndrome / COVID-19 / Mucocutaneous Lymph Node Syndrome Type of study: Observational study / Prognostic study Topics: Long Covid Limits: Adolescent / Child / Humans Language: English Journal: Nat Rev Rheumatol Journal subject: Rheumatology Year: 2021 Document Type: Article Affiliation country: S41584-021-00709-9