Incomplete Kawasaki sindrome followed by systemic onset-juvenile idiopathic arthritis mimicking Kawasaki syndrome.

Donato Rigante, Piero Valentini, Angelica Bibiana Delogu, Roberta Onesimo, Donatella Francesca Angelone, Alessia De Nisco, Iliana Bersani

Research output: Contribution to journalArticle

Abstract

A 3-month-old child was first treated for incomplete Kawasaki syndrome with three cycles of intravenous immunoglobulins and aspirin, then with methylprednisolone which led to fever remission. The same child was re-hospitalized after a 10-month-period of well-being for the suspicion of a new episode of Kawasaki syndrome, which appeared to be immunoglobulin-resistant: extensive testing failed to provide an alternative diagnosis of any infectious or infiltrative disease. Diagnosis of systemic onset-juvenile idiopathic arthritis was postulated upon the long persistence of fever and inflammatory signs, which subsided only after starting corticosteroid treatment.
Original languageEnglish
Pages (from-to)535-539
Number of pages5
JournalRheumatology International
Publication statusPublished - 2010

Keywords

  • Kawasaki Syndrome

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