Skip to main content
Top
Published in: BMC Pediatrics 1/2017

Open Access 01-12-2017 | Case report

A child with resistant Kawasaki disease successfully treated with anakinra: a case report

Authors: J. Sánchez-Manubens, A. Gelman, N. Franch, S. Teodoro, J. R. Palacios, N. Rudi, J. Rivera, J. Antón

Published in: BMC Pediatrics | Issue 1/2017

Login to get access

Abstract

Background

Kawasaki disease (KD) is an acute self-limited systemic vasculitis of unknown etiology. Intravenous immunoglobulin (IVIG) is an effective treatment and decreases the risk of cardiac complications to less than 5%. In spite of its effectiveness, some children do not respond to this therapy and still develop coronary aneurysms (CAA). The optimal treatment for IVIG non-responsive patients remains controversial although corticoids have been suggested to be an effective treatment in some patients. For those patients still resistant to IVIG and corticoids, interleukin-1 receptor antagonists (IL-1RA) such anakinra could be an alternative.

Case presentation

We present a 3 year-old Caucasian patient with KD without cardiac complications but with important resistance to treatment. After becoming resistant to IVIG and corticoids, anakinra proved to be an effective treatment.

Conclusions

To our knowledge, this is the first report of the utility of IL-1RA in refractory KD without coronary impairment. The patient fulfilled the classical criteria for KD and, after becoming resistant to first and second line treatments, anakinra proved to be an effective treatment. Further studies are required to determine if this is an effective treatment option for other cases of resistant Kawasaki disease.
Literature
1.
go back to reference Newburger JW, Takahashi M, Gerber MA, et al. Diagnosis, treatment, and long-term management of Kawasaki disease: a statement for health professionals from the committee on rheumatic fever, Endocarditis, and Kawasaki disease, council on cardiovascular disease in the young, American Heart Association. Pediatrics. 2004;114:1708–33. doi:10.1542/peds.2004-2182.CrossRefPubMed Newburger JW, Takahashi M, Gerber MA, et al. Diagnosis, treatment, and long-term management of Kawasaki disease: a statement for health professionals from the committee on rheumatic fever, Endocarditis, and Kawasaki disease, council on cardiovascular disease in the young, American Heart Association. Pediatrics. 2004;114:1708–33. doi:10.​1542/​peds.​2004-2182.CrossRefPubMed
3.
11.
go back to reference Onouchi Y, Suzuki Y, Suzuki H, et al. ITPKC and CASP3 polymorphisms and risks for IVIG unresponsiveness and coronary artery lesion formation in Kawasaki disease. Pharmacogenomics J. 2013;13:52–9. doi:10.1038/tpj.2011.45.CrossRefPubMed Onouchi Y, Suzuki Y, Suzuki H, et al. ITPKC and CASP3 polymorphisms and risks for IVIG unresponsiveness and coronary artery lesion formation in Kawasaki disease. Pharmacogenomics J. 2013;13:52–9. doi:10.​1038/​tpj.​2011.​45.CrossRefPubMed
Metadata
Title
A child with resistant Kawasaki disease successfully treated with anakinra: a case report
Authors
J. Sánchez-Manubens
A. Gelman
N. Franch
S. Teodoro
J. R. Palacios
N. Rudi
J. Rivera
J. Antón
Publication date
01-12-2017
Publisher
BioMed Central
Published in
BMC Pediatrics / Issue 1/2017
Electronic ISSN: 1471-2431
DOI
https://doi.org/10.1186/s12887-017-0852-6

Other articles of this Issue 1/2017

BMC Pediatrics 1/2017 Go to the issue