R. Noda et al., Cardiac imaging in a patient with anomalous origin of the left coronary artery from the pulmonary artery - A case report, ANGIOLOGY, 52(8), 2001, pp. 567-571
Anomalous origin of the left coronary artery from the pulmonary artery (ALC
APA) is an uncommon congenital heart disease and has a high mortality rate
in infancy. However, myocardial ischemia does not develop until adolescence
or adulthood in about 10% of patients. Moreover, the diagnosis of ALCAPA i
s often difficult in cases without heart murmur or cardiac symptoms. The au
thors report the case of a 31-year-old man with ALCAPA. He was admitted to
the hospital for evaluation of mild shortness of breath at exercise, but he
had no typical chest symptoms due to myocardial ischemia or heart failure
until age 31 and he had no heart murmur. Moreover, electrocardiogram did no
t show an old myocardial infarction or myocardial ischemia. Therefore, the
authors did not suspect ALCAPA until they performed transthoracic echocardi
ography and exercise-stress single photon emission computed tomography (SPE
CT) with Tc-99m-tetrofosmin. The final diagnosis was established from the r
esults of coronary arteriography. In the present case, a transthoracic echo
cardiogram showed abnormal coronary circulation, and exercise-stress SPECT
revealed reversible myocardial ischemia. Transthoracic echocardiography and
myocardial SPECT imaging could be a useful noninvasive tools for diagnosin
g the ALCAPA.