Coarctation represents 5-8% of congenital heart disease.We present here a
study which aimed to assess the results of this malformation correction by using left subclavian artery
flap aortoplasty technique(Waldhausen) and compare these results with those of other surgical options.
Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital
anomaly. It presents predominantly in infancy with features of myocardial ischemia or cardiac failure and
may be mistaken for common pediatric cond
itions such as colic, reflux or bronchiolitis. With early
surgical correction the prognosis is good. In this report we present unusual case of a 5-year-old female
with an anomalous left coronary artery arising from the pulmonary artery (ALCAPA) presenting with
chest pain,dyspnea and palpitation during physical exertion.Trans-thoracic echocardiography and
coronary angiography revealed an anomalous origin of the left coronary artery with mitral regurgitation .
She subsequently underwent successful surgical technique where the left internal thoracic(mammary)
artery was used to revascularise the left main coronary artery which is considered as the first unique
procedure in children. Excellent surgical results were obtained and the patient was discharged from the
hospital without complaints.
