• 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