Preoperative three-dimensional 64-row multidetector com

Abnormal origin of the left subclavian artery from the left pulmonary artery in a patient with double outlet right ventricle. Lee Y, Hong SW - Korean J Thorac Cardiovasc Surg (2014) Bottom Line: Anomalous aortic origin of the left subclavian artery (LSCA) from the left pulmonary artery (LPA) is a rare congenital cardiac malformation.We describe a case of LSCA from the LPA via ductus arteriosus in association with a double-outlet right ventricle, which never has been reported previously in Korea. View Article: PubMed Central - PubMed Affiliation: Department of Thoracic and Cardiovascular Surgery, Kyungpook National University School of Medicine, Korea. ABSTRACT Anomalous aortic origin of the left subclavian artery (LSCA) from the left pulmonary artery (LPA) is a rare congenital cardiac malformation. We describe a case of LSCA from the LPA via ductus arteriosus in association with a double-outlet right ventricle, which never has been reported previously in Korea. No MeSH data available. Related in: MedlinePlus	© Copyright Policy - open-access Related In: Results - Collection License Show All Figures getmorefigures.php?uid=PMC3928260&req=5 Figure 1: Preoperative three-dimensional 64-row multidetector computed tomography showed the LSCA arising from LPA via PDA. LSCA, left subclavian artery; LPA, left pulmonary artery; PDA, patent ductus arteriosus; LCCA, left common carotid artery; RCCA, right common carotid artery; RSCA, right subclavian artery. Mentions: Two-dimensional echocardiography demonstrated the right aortic arch, anterior malalignment ventricular septal defect, overriding aorta (60%), and pulmonary and infundibular stenosis. These findings were consistent with DORV, Fallot type. Patent ductus arteriosus (PDA) arose from a tortuous abnormal artery with bidirectional shunting. The left subclavian artery (LSCA) was not seen arising from the aorta. However, three-dimensional 64-row multidetector computed tomography (MDCT) showed the LSCA arising from the left pulmonary artery via ductus arteriosus (Fig. 1). Associated non-cardiac anomalies were also determined and included inguinal hernia, polydactyly, and syndactyly. The fluorescent in situ hybridization test was positive for the DiGeorge syndrome (22q11 deletion).

Abnormal origin of the left subclavian artery from the left pulmonary artery in a patient with double outlet right ventricle.

Lee Y, Hong SW - Korean J Thorac Cardiovasc Surg (2014)

Bottom Line: Anomalous aortic origin of the left subclavian artery (LSCA) from the left pulmonary artery (LPA) is a rare congenital cardiac malformation.We describe a case of LSCA from the LPA via ductus arteriosus in association with a double-outlet right ventricle, which never has been reported previously in Korea.

View Article: PubMed Central - PubMed

Affiliation: Department of Thoracic and Cardiovascular Surgery, Kyungpook National University School of Medicine, Korea.

ABSTRACT

Anomalous aortic origin of the left subclavian artery (LSCA) from the left pulmonary artery (LPA) is a rare congenital cardiac malformation. We describe a case of LSCA from the LPA via ductus arteriosus in association with a double-outlet right ventricle, which never has been reported previously in Korea.

No MeSH data available.

Related in: MedlinePlus

Preoperative three-dimensional 64-row multidetector computed tomography showed the LSCA arising from LPA via PDA. LSCA, left subclavian artery; LPA, left pulmonary artery; PDA, patent ductus arteriosus; LCCA, left common carotid artery; RCCA, right common carotid artery; RSCA, right subclavian artery.

Related In: Results - Collection

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Figure 1: Preoperative three-dimensional 64-row multidetector computed tomography showed the LSCA arising from LPA via PDA. LSCA, left subclavian artery; LPA, left pulmonary artery; PDA, patent ductus arteriosus; LCCA, left common carotid artery; RCCA, right common carotid artery; RSCA, right subclavian artery.

Mentions: Two-dimensional echocardiography demonstrated the right aortic arch, anterior malalignment ventricular septal defect, overriding aorta (60%), and pulmonary and infundibular stenosis. These findings were consistent with DORV, Fallot type. Patent ductus arteriosus (PDA) arose from a tortuous abnormal artery with bidirectional shunting. The left subclavian artery (LSCA) was not seen arising from the aorta. However, three-dimensional 64-row multidetector computed tomography (MDCT) showed the LSCA arising from the left pulmonary artery via ductus arteriosus (Fig. 1). Associated non-cardiac anomalies were also determined and included inguinal hernia, polydactyly, and syndactyly. The fluorescent in situ hybridization test was positive for the DiGeorge syndrome (22q11 deletion).