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Levoatriocardinal vein with normal intracardiac anatomy and pulmonary venous return
Levoatriocardinal vein (LACV) is characterized by an abnormal connection between pulmonary and systemic venous return. This extremely rare cardiac malformation is usually associated with left-sided obstructive lesions including mitral atresia, hypoplastic left-heart syndrome, and abnormal pulmonary...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180981/ https://www.ncbi.nlm.nih.gov/pubmed/21976883 http://dx.doi.org/10.4103/0974-2069.84667 |
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author | Odemis, Ender Akdeniz, Celal Saygili, Ozlem Barutcu Karaci, Ali Riza |
author_facet | Odemis, Ender Akdeniz, Celal Saygili, Ozlem Barutcu Karaci, Ali Riza |
author_sort | Odemis, Ender |
collection | PubMed |
description | Levoatriocardinal vein (LACV) is characterized by an abnormal connection between pulmonary and systemic venous return. This extremely rare cardiac malformation is usually associated with left-sided obstructive lesions including mitral atresia, hypoplastic left-heart syndrome, and abnormal pulmonary venous connection. Patients may have low systemic cardiac output and pulmonary venous obstruction symptoms. In this manuscript, we report a case with LACV and normal pulmonary venous return with absence of any intracardiac pathology. LACV was demonstrated with echocardiography, angiography, and computed tomography. Surgical correction was made successfully. |
format | Online Article Text |
id | pubmed-3180981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-31809812011-10-04 Levoatriocardinal vein with normal intracardiac anatomy and pulmonary venous return Odemis, Ender Akdeniz, Celal Saygili, Ozlem Barutcu Karaci, Ali Riza Ann Pediatr Cardiol Case Report Levoatriocardinal vein (LACV) is characterized by an abnormal connection between pulmonary and systemic venous return. This extremely rare cardiac malformation is usually associated with left-sided obstructive lesions including mitral atresia, hypoplastic left-heart syndrome, and abnormal pulmonary venous connection. Patients may have low systemic cardiac output and pulmonary venous obstruction symptoms. In this manuscript, we report a case with LACV and normal pulmonary venous return with absence of any intracardiac pathology. LACV was demonstrated with echocardiography, angiography, and computed tomography. Surgical correction was made successfully. Medknow Publications 2011 /pmc/articles/PMC3180981/ /pubmed/21976883 http://dx.doi.org/10.4103/0974-2069.84667 Text en © Annals of Pediatric Cardiology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Odemis, Ender Akdeniz, Celal Saygili, Ozlem Barutcu Karaci, Ali Riza Levoatriocardinal vein with normal intracardiac anatomy and pulmonary venous return |
title | Levoatriocardinal vein with normal intracardiac anatomy and pulmonary venous return |
title_full | Levoatriocardinal vein with normal intracardiac anatomy and pulmonary venous return |
title_fullStr | Levoatriocardinal vein with normal intracardiac anatomy and pulmonary venous return |
title_full_unstemmed | Levoatriocardinal vein with normal intracardiac anatomy and pulmonary venous return |
title_short | Levoatriocardinal vein with normal intracardiac anatomy and pulmonary venous return |
title_sort | levoatriocardinal vein with normal intracardiac anatomy and pulmonary venous return |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180981/ https://www.ncbi.nlm.nih.gov/pubmed/21976883 http://dx.doi.org/10.4103/0974-2069.84667 |
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