Document Detail


A rare association of major aorto-pulmonary collaterals with right isomerism and totally anomalous pulmonary venous drainage.
MedLine Citation:
PMID:  16297260     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A female neonate, born at term, presented with complex cardiac anatomy dominated by right isomerism and infra-diaphragmatic totally anomalous pulmonary venous connection. Surgical repair was performed using circulatory arrest under deep hypothermia. In the postoperative period, the patient could not be weaned off mechanical ventilation, and underwent cardiac catheterization. This revealed major aortopulmonary collateral arteries, which were occluded with coils. We review the literature with specific focus on the occurrence of this unusual combination and its implication in the management during the postoperative period.
Authors:
Sanjay Kumar; Junaid Ansari; Nihal Weerasena
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Cardiology in the young     Volume:  15     ISSN:  1047-9511     ISO Abbreviation:  Cardiol Young     Publication Date:  2005 Dec 
Date Detail:
Created Date:  2005-11-21     Completed Date:  2006-02-16     Revised Date:  2007-05-24    
Medline Journal Info:
Nlm Unique ID:  9200019     Medline TA:  Cardiol Young     Country:  England    
Other Details:
Languages:  eng     Pagination:  643-6     Citation Subset:  IM    
Affiliation:
Department of Cardiothoracic Surgery, Yorkshire Heart Centre, Leeds General Infirmary, Leeds, United Kingdom. sanjaykr33@hotmail.com
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MeSH Terms
Descriptor/Qualifier:
Aorta, Thoracic / abnormalities*
Collateral Circulation
Coronary Angiography
Embolization, Therapeutic
Female
Heart Catheterization
Heart Defects, Congenital / surgery*
Humans
Hyperthermia, Induced
Infant, Newborn
Pulmonary Veins / abnormalities*
Comments/Corrections
Comment In:
Cardiol Young. 2006 Dec;16(6):608; author reply 609   [PMID:  17116278 ]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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