scholarly journals Distinct characteristics of multisystem inflammatory syndrome in children in Poland

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Kamila Maria Ludwikowska ◽  
Magdalena Okarska-Napierała ◽  
Natalia Dudek ◽  
Paweł Tracewski ◽  
Jacek Kusa ◽  
...  

AbstractDuring the winter months of 2020/2021 a wave of multisystem inflammatory syndrome in children (MIS-C) emerged in Poland. We present the results of a nationwide register aiming to capture and characterise MIS-C with a focus on severity determinants. The first MIS-C wave in Poland was notably high, hence our analysis involved 274 children. The group was 62.8% boys, with a median age of 8.8 years. Besides one Asian, all were White. Overall, the disease course was not as severe as in previous reports, however. Pediatric intensive care treatment was required for merely 23 (8.4%) of children, who were older and exhibited a distinguished clinical picture at hospital admission. We have also identified sex-dependent differences; teenage boys more often had cardiac involvement (decreased ejection fraction in 25.9% vs. 14.7%) and fulfilled macrophage activation syndrome definition (31.0% vs. 15.2%). Among all boys, those hospitalized in pediatric intensive care unit were significantly older (median 11.2 vs. 9.1 years). Henceforth, while ethnicity and sex may affect MIS-C phenotype, management protocols might be not universally applicable, and should rather be adjusted to the specific population.

2012 ◽  
Vol 13 (5) ◽  
pp. 616-617 ◽  
Author(s):  
Tellen D. Bennett ◽  
Kristen N. Hayward ◽  
Sarah Ringold ◽  
Carol A. Wallace ◽  
Reid W.D. Farris ◽  
...  

2021 ◽  
Vol 2021 (6) ◽  
Author(s):  
Nadia Ahmad ◽  
Aneel Parmar ◽  
Joanne Kitchen

ABSTRACT Anti-synthetase syndrome (ASS) is an autoimmune disease characterized by autoantibodies against an aminoacyl transfer RNA synthetase with clinical features including interstitial lung disease, non-erosive arthritis, myositis, Raynaud’s phenomenon, unexplained fever and/or mechanic’s hands. Macrophage activation syndrome (MAS) is a potentially fatal hyper- inflammatory syndrome that can occur as a complication of systemic rheumatic diseases. However, the association of MAS and ASS has rarely been reported in the literature. Here, we report this association in a patient with overlap ASS and anti-CCP positive rheumatoid arthritis. First line management with steroids was complicated by diabetic ketoacidosis, hence requiring use of anti-IL1 therapy (anakinra) for disease control.


Author(s):  
Aman Gupta ◽  
Arpinder Gill ◽  
Manu Sharma ◽  
Megha Garg

Abstract There have been recent reports of children presenting with severe multi-system hyperinflammatory syndrome resembling Kawasaki disease (KD) during current COVID-19 pandemic. Exact pathophysiology is unknown, however, most of the children have multi-organ dysfunction and respiratory system involvement is less common compared to adults. These patients have certain characteristic laboratory parameters different from those seen in children with KD. However, only limited literature is available at present for identification and management of such patients. We report a young girl who presented with fever, rash and other manifestations mimicking classic KD and fulfilling the case definitions for pediatric multi-system inflammatory syndrome. She had lymphopenia, thrombocytopenia and hyponatremia in the absence of macrophage activation syndrome, similar to that seen in patients reported from UK and Italy. Clinical manifestations resolved and laboratory parameters improved with intravenous immunoglobulin and corticosteroids. Early recognition is important to administer immunomodulatory therapy which may be life saving for these patients.


2021 ◽  
Author(s):  
Miguel García‐Domínguez ◽  
Cynthia G. Torres ◽  
Juan M. Carreón‐Guerrero ◽  
Jose Quibrera ◽  
Daniela Arce‐Cabrera ◽  
...  

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