Literature DB >> 15311170

Anomalous origin of the coronary arteries from the pulmonary trunk in two separate patients with a review of the clinical implications and current treatment recommendations.

William J Nicholson1, Brian Schuler, Stamatios Lerakis, Tarek Helmy.   

Abstract

Anomalous origin of a coronary artery from the pulmonary artery (PA) is an unusual abnormality. These anomalies are often hemodynamically significant and can lead to myocardial ischemia, myocardial infarction, and sudden cardiac death. Anomalous origin of the left coronary artery (LCA) from the pulmonary trunk is known as Bland-White-Garland syndrome and causes death in 80% to 85% of affected children in the first year of life. Treatment of the LCA arising from the PA is typically surgical, with ligation and reimplantation of the LCA to the aorta. In contrast, origination of the right coronary artery from the PA is usually a benign anomaly, although clinically significant sequelae can develop. Controversy exists regarding the need to intervene in the cases of patients with this usually incidentally discovered anomaly. We review the clinical presentation and treatment of patients with each anomaly and the current recommendations regarding the clinical course and management of such patients.

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Year:  2004        PMID: 15311170     DOI: 10.1097/00000441-200408000-00007

Source DB:  PubMed          Journal:  Am J Med Sci        ISSN: 0002-9629            Impact factor:   2.378


  1 in total

1.  Double anomalous coronary origin from the pulmonary artery: successful surgical correction in an infant.

Authors:  Enrique Ochoa-Ramírez; Hector E Valdez-Garza; Roberto Reyes-González; Dimas Mateos-Corral; David Sánchez-Sigel; Valeria González-López
Journal:  Tex Heart Inst J       Date:  2005
  1 in total

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