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. 2023 Jan 16;56(2):236–245. doi: 10.1016/j.jmii.2023.01.001

Table 3.

Comparisons of multisystem inflammatory syndrome in children (MIS-C) and Kawasaki disease.

Demographics MIS-C Kawasaki disease
Age ≤20 years, peak 6–11 years <5 years
Male: female ratio 3:2 1.5:1
Ethnicity High incidence in Japan, China, Taiwan, South Korea High incidence in children of African and Hispanic heritage
Clinical features
Fever 100% (+), ≥1 day 100% (+), ≥5 days
Conjunctival injection 31%–83% >90%
Red, fissured lips 30%–50% >90%
Strawberry tongue 10% >90%
Cervical lymphadenopathy 20%–70% 20%–70%
Skin rashes 50%–70% >90%
Morphology Macule, papules, urticarial-like, petechia, purpura Macule, papules, urticarial-like
BCG scar erythema rare 30%–40%
Palmar/plantar edema and erythema 26%–68% 75%
Shock 40%–80% 2%–7%
Gastrointestinal symptom 60%–100% 20%
Dyspnea 19%–29% Rare
Neurological symptom 13%–35% 5%–39%
Laboratory findings
Lymphopenia 37%–81% rare
Thrombocytopenia 11%–31% Uncommon
Inflammatory markers Increased ∼100% Increased ∼100%
Increased troponin 33%–95% rare
Increased proBNP 73%–95% rare
Increased ferritin 54%–75% rare
Increased D-dimer 91%–98% rare
Sterile pyuria 50% 50%
Coronary artery dilatation 14%–48% 10%–30%
Mortality rate 1%–3% <0.5%

BCG, Bacillus Calmette-Guérin; proBNP, pro-brain natriuretic peptide.