Literature DB >> 26140805

Anomalous Left Coronary From the Pulmonary Artery Presenting as Ventricular Fibrillation After Persistent Ductus Arteriosus Ligation.

Daniel P Fudulu1, Robert M R Tulloh2, Andrew R Wolf2, Andrew J Parry2, Serban C Stoica2.   

Abstract

An anomalous left coronary artery from the pulmonary artery (ALCAPA) is rarely associated with persistent ductus arteriosus (PDA). A large PDA can maintain perfusion in the left coronary artery, delaying presentation. Assessing the origin of the coronary arteries before PDA ligation is difficult, often being performed in very small or even preterm babies. We present the case of a 5-month-old infant with echocardiographic features of mitral regurgitation and subendocardial ischemia who experienced ischemia and cardiac arrest after PDA ligation. Transesophageal echocardiography demonstrated ALCAPA, and left coronary translocation was performed. The infant was discharged after 10 days.
Copyright © 2015 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.

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Year:  2015        PMID: 26140805     DOI: 10.1016/j.athoracsur.2015.04.015

Source DB:  PubMed          Journal:  Ann Thorac Surg        ISSN: 0003-4975            Impact factor:   4.330


  2 in total

1.  Anomalous Origin of the Right Coronary Artery from the Pulmonary Artery in a Neonate with Turner Syndrome and Aortic Arch Hypoplasia.

Authors:  Bryan P Stefek; Jason R Imundo; Joseph B Clark
Journal:  Tex Heart Inst J       Date:  2019-06-01

2.  Neonatal ventricular fibrillation and an elusive ALCAPA: things are not always as they seem.

Authors:  Tracie C Walker; Markus S Renno; David A Parra; Scott O Guthrie
Journal:  BMJ Case Rep       Date:  2016-03-31
  2 in total

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