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Angiology
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Bilateral Coronary-Artery-to-Pulmonary-Artery Fistula Coexistent with Apical Hypertrophic Cardiomyopathy— A Case Report

Yau-Ting Tai, M.B., M.R.C.P., F.A.C.A.

Division of Cardiology, Department of Medicine, University of Hong Kong, Hong Kong

Ping-Ching Fong, M.B., M.R.C.P.

Division of Cardiology, Department of Medicine, University of Hong Kong, Hong Kong

Wing-Hing Chow, M.B., M.R.C.P., F.I.C.A.

Division of Cardiology, Department of Medicine, University of Hong Kong, Hong Kong

A sixty-four-year-old man presented with repolarization abnormalities on the electrocardiogram. Echocardiography and cardiac catheterization revealed that he had the rare combination of apical hypertrophic cardiomyopathy with bilateral coronary-artery-to-pulmonary-artery fistula. An exercise thallium scan was negative, suggesting that the marked electrocardiographic changes were most likely secondary to the apical myocardial hypertrophy, instead of to coronary-steal-induced ischemia.

Angiology, Vol. 43, No. 1, 72-75 (1992)
DOI: 10.1177/000331979204300109
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This article has been cited by other articles:


Home page
 Ann. Thorac. Surg.Home page
A. S. Olearchyk, D. M. Runk, M. Alavi, and M. A. Grosso
Congenital Bilateral Coronary-to-Pulmonary Artery Fistulas
Ann. Thorac. Surg., July 1, 1997; 64(1): 233 - 235.
[Abstract] [Full Text]


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