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A Case of Aortopulmonary Window: Asymptomatic until the First Pregnancy
The aortopulmonary window (APW) is an abnormal communication between the ascending aorta and the pulmonary trunk in the presence of two separate semilunar valves. It is a rare congenital malformation which represents 0.1% of all congenital cardiac diseases. Herein, we report a very rare case of 27-y...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4589611/ https://www.ncbi.nlm.nih.gov/pubmed/26457208 http://dx.doi.org/10.1155/2015/935253 |
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author | Kose, Murat Ucar, Serra Emet, Samim Akpinar, Timur Selcuk Yalin, Kıvanc |
author_facet | Kose, Murat Ucar, Serra Emet, Samim Akpinar, Timur Selcuk Yalin, Kıvanc |
author_sort | Kose, Murat |
collection | PubMed |
description | The aortopulmonary window (APW) is an abnormal communication between the ascending aorta and the pulmonary trunk in the presence of two separate semilunar valves. It is a rare congenital malformation which represents 0.1% of all congenital cardiac diseases. Herein, we report a very rare case of 27-year-old patient with unrepaired APW causing Eisenmenger syndrome and pulmonary hypertension who was asymptomatic until her first pregnancy. The median survival of uncorrected APW is 33 years. Aortopulmonary window is a very rare congenital anomaly. To our knowledge, asymptomatic adult case has not been reported until now. APW should be considered in the differential diagnosis of the severe pulmonary hypertension also in adult patients. |
format | Online Article Text |
id | pubmed-4589611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-45896112015-10-11 A Case of Aortopulmonary Window: Asymptomatic until the First Pregnancy Kose, Murat Ucar, Serra Emet, Samim Akpinar, Timur Selcuk Yalin, Kıvanc Case Rep Cardiol Case Report The aortopulmonary window (APW) is an abnormal communication between the ascending aorta and the pulmonary trunk in the presence of two separate semilunar valves. It is a rare congenital malformation which represents 0.1% of all congenital cardiac diseases. Herein, we report a very rare case of 27-year-old patient with unrepaired APW causing Eisenmenger syndrome and pulmonary hypertension who was asymptomatic until her first pregnancy. The median survival of uncorrected APW is 33 years. Aortopulmonary window is a very rare congenital anomaly. To our knowledge, asymptomatic adult case has not been reported until now. APW should be considered in the differential diagnosis of the severe pulmonary hypertension also in adult patients. Hindawi Publishing Corporation 2015 2015-09-17 /pmc/articles/PMC4589611/ /pubmed/26457208 http://dx.doi.org/10.1155/2015/935253 Text en Copyright © 2015 Murat Kose et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Kose, Murat Ucar, Serra Emet, Samim Akpinar, Timur Selcuk Yalin, Kıvanc A Case of Aortopulmonary Window: Asymptomatic until the First Pregnancy |
title | A Case of Aortopulmonary Window: Asymptomatic until the First Pregnancy |
title_full | A Case of Aortopulmonary Window: Asymptomatic until the First Pregnancy |
title_fullStr | A Case of Aortopulmonary Window: Asymptomatic until the First Pregnancy |
title_full_unstemmed | A Case of Aortopulmonary Window: Asymptomatic until the First Pregnancy |
title_short | A Case of Aortopulmonary Window: Asymptomatic until the First Pregnancy |
title_sort | case of aortopulmonary window: asymptomatic until the first pregnancy |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4589611/ https://www.ncbi.nlm.nih.gov/pubmed/26457208 http://dx.doi.org/10.1155/2015/935253 |
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