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Patients with this condition present with some clinical features similar to those of Kawasaki disease (KD) and display signs and symptoms that are uncommon or rarely occur in this disorder, such as gastrointestinal complaints and myocarditis, often leading to myocardial failure and shock. In addition, patients\u2019 age is older than that of children with classic KD. Management is based on administering intravenous immunoglobulin, glucocorticoids, and anakinra in the most severe instances. It is still debated whether MIS\u2010C and KD are different illnesses or represent a disease continuum.<\/jats:p>","DOI":"10.1111\/pai.13645","type":"journal-article","created":{"date-parts":[[2022,1,26]],"date-time":"2022-01-26T06:30:22Z","timestamp":1643178622000},"page":"102-104","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":5,"title":["Childhood multisystem inflammatory syndrome associated with COVID\u201019 (MIS\u2010C): Distinct from Kawasaki disease or part of the same spectrum?"],"prefix":"10.1111","volume":"33","author":[{"given":"Maria","family":"Santaniello","sequence":"first","affiliation":[{"name":"Dipartimento di Neuroscienze, Riabilitazione, Oftalmologia Genetica e Scienze Materno\u2010Infantili Universit\u00e0 degli Studi di Genova  Genoa 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