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Differences and similarities of multisystem inflammatory syndrome in children, Kawasaki disease and macrophage activating syndrome due to systemic juvenile idiopathic arthritis: a comparative study.

Gülçin Otar YenerAyşenur Paç KısaarslanKadir UluErdal AtalayFatih HaslakSemanur OzdelBurcu Bozkaya YücelDeniz Gezgin YıldırımFigen CakmakKübra OztürkMustafa CakanZeynep BalikCanan Hasbal AkkusMehmet YildizTugba EratBenhur Şirvan ÇetinMünevver YılmazEsra BaglanSibel Lacinel GurlevikVildan AtasayanSerife Gül KaradagAmra AdrovicŞengül ÇağlayanAyşe TanatarFatma Gül DemirkanTaner CoşkunerÖzlem AkgünMuserref Kasap CuceogluGülşah Kavrul KayaalpSezgin ŞahinÖzge BasaranFerhat DemirKenan BarutMurat ÇiftelDolunay GürsesAli BaykanYasemin ÖzsürekciTevfik KaragözHafize Emine SönmezYelda BilginerNuray Aktay AyazÖzlem AydoğSelcuk YukselBetul SozeriOzgur KasapcopurSeher Sener
Published in: Rheumatology international (2021)
To compare the clinical and laboratory findings of multisystem inflammatory syndrome in children (MIS-C), patients with Kawasaki disease (KD) and with macrophage activating syndrome due to systemic juvenile idiopathic arthritis (sJIA-MAS) on real-life data. Patients diagnosed with MIS-C, KD, and sJIA-MAS from 12 different centers in Turkey who were followed for at least 6 months were included in the study. Demographic, clinical, and laboratory findings of all patients were analyzed. A total of 154 MIS-C, 59 KD, and 31 sJIA-MAS patients were included. The median age of patients with MIS-C were higher than those with KD while lower than those with sJIA-MAS (8.2, 3, 12 years, respectively). Myalgia (39.6%), cardiac (50.6%), gastrointestinal (72.7%), and neurological (22.1%) involvements were more common in patients with MIS-C compared to others. MIS-C patients had lower levels of lymphocyte (950 vs 1700 cells/µl) and thrombocyte (173,000 vs 355,000 cells/µl) counts and higher pro-BNP (1108 vs 55 pg/ml) levels than KD. Ferritin levels were higher in patients with MIS-C compared to patients with KD while they were lower than patients with sJIA-MAS (440, 170, 10,442 ng/ml, respectively). Patients with MIS-C had a shorter duration of hospitalization than sJIA-MAS (p = 0.02) while they required intensive care unit admission more frequently (55 vs 8 patients, p < 0.001). The median MAS/sJIA score of MIS-C patients was - 1.64 (- 5.23 to 9.68) and the median MAS/sJIA score of sJIA-MAS patients was -2.81 ([- 3.79] to [- 1.27]). MIS-C patients displayed certain differences in clinical and laboratory features when compared to KD and sJIA-MAS. Definition of the differences and similarities between MIS-C and the other intense inflammatory syndromes of childhood such as KD and MAS will help the clinicians while making timely diagnosis.
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