Prenatal diagnosis of anomalous origin of the right pulmonary artery from the ascending aorta.
نویسندگان
چکیده
We report a case of anomalous origin of the right pulmonary artery from the ascending aorta that was diagnosed by fetal ultrasound at 21 weeks of gestation. The clue to the diagnosis was present in the three-vessel view, this being one of the views that we use for fetal cardiac screening. The anomaly was corrected surgically at 11 days of age. We discuss the importance of prenatal diagnosis in the management of this rare anomaly.
منابع مشابه
Fetal Isolated Anomalous Origin of Right Pulmonary Artery from Aorta
The anomalous origin of a branch pulmonary artery from the aorta (AOPA) is characterized by the anomalous origin of one of the branch pulmonary arteries (PA) from the ascending aorta and a normal origin of the other PA from main PA. AOPA is an extremely rare cardiac malformation. Few studies have reported fetal anomalous origin of PA from aorta with other malformation. We report a case of isola...
متن کاملAnomalous origin of a pulmonary artery from the ascending aorta: surgical repair resolving pulmonary arterial hypertension.
OBJECTIVE To emphasize the diagnostic possibility of the anomalous origin of one pulmonary artery from the ascending aorta in infants with clinically refractory heart failure and no intracardiac structural defect. METHODS Retrospective study of 4 infants with refractory heart failure undergoing 2-dimensional echocardiographic study with subcostal, suprasternal, and parasternal views, and hemo...
متن کاملAortic Origin of the Right Pulmonary Artery
Surgical repair of an anomalous right pulmonary artery arising from the ascending aorta is rare. Angiocardiography is the procedure of choice in establishing the diagnosis. Surgical correction of the defect is mandatory; otherwise most of these children die in refractory heart failure. The present paper reports the first successful anatomic repair without a graft in a 2-month-old baby. Five mon...
متن کامل[Aortic origin of the left pulmonary artery in an infant with Fallot's tetralogy].
We report the case of a male neonate who had a prenatal diagnosis of Fallot's tetralogy. He presented with respiratory distress during the second week of life. Chest x-ray showed an enlarged right ventricle and pulmonary edema. Echocardiography demonstrated characteristic features of Fallot's tetralogy. However, cardiac catheterization disclosed that, in this case of Fallot's tetralogy, the lef...
متن کاملAnomalous origin of one pulmonary artery from the ascending aorta: a review of echocardiographic, catheter, and morphological features.
Six patients with anomalous origin of one pulmonary artery from the ascending aorta were reviewed. Four had anomalous origin of the right pulmonary artery and two had anomalous origin of the left pulmonary artery from the ascending aorta. Two of these six patients had tetralogy of Fallot. Two patients died in the first month of life. No changes in the pulmonary vasculature were seen at necropsy...
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ورودعنوان ژورنال:
- Kyobu geka. The Japanese journal of thoracic surgery
دوره 40 5 شماره
صفحات -
تاریخ انتشار 1961