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The Journal of Thoracic and Cardiovascular Surgery, Vol 79, 283-287, Copyright © 1980 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
FM Sandiford, TA Vargo, JY Shih, S Pelargonio and DG McNamara
A 9-year-old girl developed ischemic cardiac symptoms 3 years after she
first presented with characteristic manifestations of Kawasaki's disease,
namely, high fever, conjunctivitis, lymphadenopathy, macular truncal skin
rash, and erythema of both hands followed by desequamation of the skin of
the fingertips. This acute illness resolved spontaneously within 2 weeks.
Because of progressive and severe anginal symptoms and electrocardiographic
signs of myocardial ischemia, she underwent cardiac catheterization and
coronary angiography, which demonstrated multiple aneurysms of both right
and left coronary artery systems. The two larger aneurysms of the right
main and left main coronary arteries were clotted, causing complete
occlusion of these vessels. Only collateral branches from the proximal
right coronary artery which were supporting the entire coronary
circulation, prevented her from having a myocardial infarction. A triple
saphenous vein bypass was performed with excellent immediate results. One
year later the patient was completely free of symptoms; she was living a
normal life and a stress electrocardiogram was entirely normal.
ARTICLES
Successful triple coronary artery bypass in a child with multiple coronary aneurysms due to Kawasaki's disease
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H. Fee and E. McGough Idiopathic Multiple Systemic Aneurysms in a Child Arch Pediatr Adolesc Med, November 1, 1983; 137(11): 1101 - 1102. [Abstract] [PDF] |
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