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J Thorac Cardiovasc Surg 2007;134:1586-1587
© 2007 The American Association for Thoracic Surgery
Brief Communication |
a Department of Cardiothoracic Surgery, Birmingham Childrens Hospital, Birmingham, United Kingdom
b Department of Pediatric Cardiology, Birmingham Childrens Hospital, Birmingham, United Kingdom.
Received for publication July 25, 2007; accepted for publication August 7, 2007. * Address for reprints: William J. Brawn, FRCS, FRACS, Consultant Cardiothoracic Surgeon, Department of Cardiothoracic Surgery, Birmingham Childrens Hospital, Steelhouse Lane, Birmingham B4 6NH, United Kingdom. (Email: william.brawn@bch.nhs.uk).
| The first 20% of the full text of this article appears below. |
Occlusion of the left coronary ostium by an aortic valve leaflet is a rare but well-described variant of aortic valve morphology. We report this finding in a neonate with a number of cardiac abnormalities, substantiating the theory that it is a congenital abnormality of aortic valve development.
Clinical Summary
A 3-day-old boy who weighed 2.7 kg presented with poor feeding and lethargy after an uneventful normal vaginal delivery at term. Examination revealed tachypnea, poor peripheral pulses, and a systolic murmur. An echocardiogram revealed normal atrial arrangement, atrial septal defect with bidirectional flow, muscular outlet ventricular septal defect, subaortic stenosis (left ventricular outflow tract diameter of 4 mm), dysplastic stenotic aortic valve with a maximum root diameter of 4.8 mm (Figure 1), type A interrupted aortic arch, moderate-sized ductus arteriosus, and normal-volume left ventricle with impaired systolic function. After stabilization with prostaglandin E2 (7.5 ng/kg/min) and dobutamine (5 µg/kg/min), surgery was undertaken at 9 days.
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