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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

Postoperative three-dimensional 64-row multidetector computed tomography revealed LSCA arising from the LCCA without stenosis. LSCA, left subclavian artery; LCCA, left common carotid artery; RCCA, right common carotid artery; RSCA, right subclavian artery.
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Figure 2: Postoperative three-dimensional 64-row multidetector computed tomography revealed LSCA arising from the LCCA without stenosis. LSCA, left subclavian artery; LCCA, left common carotid artery; RCCA, right common carotid artery; RSCA, right subclavian artery.

Mentions: Fifteen months later, the patient underwent intraventricular tunnel repair of the DORV at 16 months of age. Three-dimensional 64-row MDCT at the time revealed the LSCA arising from the LCCA without stenosis (Fig. 2). The patient is now 18 months old and has normal left arm function and growth.


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)

Postoperative three-dimensional 64-row multidetector computed tomography revealed LSCA arising from the LCCA without stenosis. LSCA, left subclavian artery; LCCA, left common carotid artery; RCCA, right common carotid artery; RSCA, right subclavian artery.
© Copyright Policy - open-access
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC3928260&req=5

Figure 2: Postoperative three-dimensional 64-row multidetector computed tomography revealed LSCA arising from the LCCA without stenosis. LSCA, left subclavian artery; LCCA, left common carotid artery; RCCA, right common carotid artery; RSCA, right subclavian artery.
Mentions: Fifteen months later, the patient underwent intraventricular tunnel repair of the DORV at 16 months of age. Three-dimensional 64-row MDCT at the time revealed the LSCA arising from the LCCA without stenosis (Fig. 2). The patient is now 18 months old and has normal left arm function and growth.

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