Rheumatology Advance Access originally published online on July 15, 2006
Rheumatology 2006 45(11):1444-1445; doi:10.1093/rheumatology/kel194
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© The Author 2006. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org
Severe cutaneous manifestations in a child with refractory Kawasaki disease
Department of Pediatrics, Rheumatology Unit, University of Firenze and 1Cardiology Unit, A. Meyer Children's Hospital, Firenze, Italy
Correspondence to: Fernanda Falcini, MD, Department of Paediatrics-Rheumatology Unit, Via Pico della Mirandola 24, 50132 Firenze, Italy. E-mail: falcini@unifi.it
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| Introduction |
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SIR, We report a child with refractory Kawasaki disease (KD), who presented severe scattered crusting skin lesions as predominant manifestation of the disease.
| Case report |
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A 17-month-old boy presented to our department with a 3 day history of fever reaching 39°C, resistant to amoxicillin, along with a maculopapular rash on the face, trunk and limbs. Past medical history was unremarkable. Routine laboratory work-up revealed erythrocyte sedimentation rate (ESR) 72 mm/h, C-reactive protein (CRP) 13.67 mg/dl (nv < 0.35), haemoglobin 10 g/dl, white blood cell count 26.50 x 103/mm3, fibrinogen 837
| Discussion |
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