Table 2.
Characteristics of SARS-CoV-2-associated diseases | |||
---|---|---|---|
Parameters analyzed | SARS-CoV-2 infection | KD | MIS-C |
Pathology | Viral infection | Pediatric vasculitis | Hyperinflammatory syndrome |
Mean age of disease onset | Any | < 5 | 6–11 |
Gender predisposition (M:F ratio) | 1:1 | 1.5:1 | 1.5:1 |
Demographics | Worldwide | Japan | Hispanic and non-Hispanic Black in the USA |
Genetic predisposition | ACE deletion (D) polymorphism | Genetic polymorphism of ITPKC | Inborn errors of immunity |
Diagnostic procedure | PCR, antigen test, antibodies (reactive IgG or IgM to SARS-Cov-2) | No single specific diagnostic test | No single specific diagnostic test |
Main diagnostic markers | Reactive IgG or IgM to SARS-CoV-2 | IL-18, IL-21, Elevated N-terminal pro-BNP | IL-18, IgG against S protein, elevated N-terminal pro-BNP, lymphopenia |
Similar symptoms | Fever, cough, fatigue | Fever (> 5 days if left untreated), lymphadenopathy, mucocutaneous findings, conjunctivitis, rash | Fever, lymphadenopathy, mucocutaneous symptoms, conjunctivitis, rash |
Characteristic symptoms | Respiratory complications | Erythema and edema of extremities | Gastrointestinal findings |
Pathognomonic symptoms | N/A | Strawberry tongue | N/A |
Major complications | MIS-C | Coronary artery aneurysm | Myocardial dysfunction |
Treatment | Often self-limited | IVIG, acetylsalicylic acid | IVIG, GCS |
SARS-CoV-2 severe acute respiratory syndrome coronavirus 2, KD Kawasaki disease, MIS-C multisystem inflammatory syndrome in children, ITPKC inositol-triphosphate three kinase C, ACE angiotensin converting enzyme, PCR polymerase chain reaction, IL-18 interleukin 18, IL-21 interleukin 21, pro-BNP pro-B-type natriuretic peptide, IgG immunoglobulin G, IVIG intravenous immunoglobulin, GCS glucocorticosteroids, N/A not applicable, USA United States of America