Literature DB >> 7614492

Occlusion of the right coronary artery as sequelae of Kawasaki disease: the clinical features of 9 cases.

N Takahashi1, J Fukushige, T Hijii, H Igarashi, A Ooshima, K Ueda.   

Abstract

Among the 302 children with Kawasaki disease (KD) who were evaluated by angiography from 1973 through 1992, 9 (3.0%) had either an occlusion (OC) or segmental stenosis (SS) of the right coronary artery. The interval from the onset of KD to the recognition of OC or SS ranged from 0.5 to 7.7 years (median 4.0 years). Left coronary arterial lesions were also present in 8 of 9 patients. In spite of severe sequelae, children or young adolescents with cardiovascular system-related symptoms were unexpectedly rare. Asymptomatic patients, however, are also at risk of developing myocardial infarction since they have been shown to have a high rate of abnormalities on myocardial scintigraphy. A close observation and careful follow-up are thus considered to be indispensable.

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Year:  1995        PMID: 7614492     DOI: 10.1159/000176875

Source DB:  PubMed          Journal:  Cardiology        ISSN: 0008-6312            Impact factor:   1.869


  1 in total

1.  Calcified occlusion of the right coronary artery in Kawasaki disease: evidence of myocardial ischaemia using cardiac technetium-99m-tetrofosmin perfusion single-photon emission computed tomography.

Authors:  J Beamish; M J O'Connell; A El Khuffash; D F Duff; C J McMahon
Journal:  Arch Dis Child       Date:  2006-11       Impact factor: 3.791

  1 in total

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