Title of article
Concomitant Coronary Artery Aneurysm and Myocarditis as a Rare Manifestation of Kawasaki Disease: A Case Report
Author/Authors
Halimiasl, Aliasghar shahid beheshti university of medical sciences - Tajrish Hospital - Department of Pediatrics, تهران, ايران , Hosseini, Amir Hossein shahid beheshti university of medical sciences - Tajrish Hospital - Department of Pediatrics, تهران, ايران , Shiari, Reza shahid beheshti university of medical sciences - Mofid Children Hospital - Department of Pediatric Rheumatology, تهران, ايران , Ghadamli, Parviz shahid beheshti university of medical sciences - Tajrish Hospital - Department of Pediatrics, تهران, ايران , Mojtahedzadeh, Saeed shahid beheshti university of medical sciences - Mofid Children Hospital - Department of Pediatric Cardiology, تهران, ايران
From page
34
To page
36
Abstract
Introduction: Kawasaki disease (KD) is an acute systemic vasculitis, of unknown etiology, that mainly affects infants and young children. Although originally thought to be a benign illness, KD may prove fatal, especially if the diagnosis is delayed due to a nonclassic presentation. Case presentation: Here, we present the case of a 4-year-old girl with a history of prolonged fever. Her physical examination and echocardiography revealed aneurysmal dilatation of the coronary arteries and myocarditis in the absence of other principal features of KD. This patient was diagnosed as having KD and responded very quickly to a high dose of intravenous immunoglobulin therapy. Discussion: This case study highlights congestive myocarditis as an atypical presentation of KD and the need to maintain a high level of awareness of this problem, in order to diagnose and treat this potentially life-threatening condition promptly.
Keywords
Mucocutaneous Lymph Node Syndrome , Coronary Aneurysm , Echocardiography
Journal title
Journal of Comprehensive Pediatrics
Journal title
Journal of Comprehensive Pediatrics
Record number
2619764
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