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New Indian Journal of Surgery 11(4):p 565-567, October-December 2020. | DOI: https://dx.doi.org/10.21088/nijs.0976.4747.11420.20
Case Report
A Rare Case of Double Chambered Right Ventricle with Anomalous Left Anterior Descending Coronary Artery from Pulmonary Artery (ALADAPA)
Anupama Rao , Anupama Rao1 , Vijay L2 , Sathya Patnaik3 , P K Dash4
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New Indian Journal of Surgery 11(4):p 565-567, October-December 2020. | DOI: https://dx.doi.org/10.21088/nijs.0976.4747.11420.20
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Anupama Rao, Vijay L, Sathya Patnaik, et al. A Rare Case of Double Chambered Right Ventricle with Anomalous Left Anterior
Descending Coronary Artery from Pulmonary Artery (ALADAPA). New Indian J Surg. 2020;11(4):565–567.
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Abstract
Double-chambered right ventricle (DCRV) is a rare congenital heart disease in which the right ventricle (RV) is hypertrophied due to anomalous muscle bundles. Anomalous left coronary artery from pulmonary artery (ALCAPA) is also a rare lesion constituting 1 in 3,00,000 live births. Isolated LAD from pulmonary artery (ALADAPA) is further rare. We report a case of DCRV associated with Anomalous left anterior descending Artery from Pulmonary artery (ALADAPA). The patient was initially diagnosed to have DCRV and on further evaluation associated anomalous left anterior descending artery from pulmonary artery was detected. The patient underwent DCRV repair and Takauchi repair and had an uneventful post operative recovery.
Keywords: Congenital Heart Disease; Double Chamber Right Ventricle; DCRV; ALCAPA; ALADAPA.
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Anupama Rao, Vijay L, Sathya Patnaik, et al. A Rare Case of Double Chambered Right Ventricle with Anomalous Left Anterior
Descending Coronary Artery from Pulmonary Artery (ALADAPA). New Indian J Surg. 2020;11(4):565–567.
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DOI: https://dx.doi.org/10.21088/nijs.0976.4747.11420.20
Keywords
Congenital Heart Disease; Double Chamber Right Ventricle; DCRV; ALCAPA; ALADAPA.Search for Similar Articles
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