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Prenatal Diagnosis and Successful Palliation of Absent Aortic Valve with Hypoplastic Left Heart Syndrome: A Case Report and Review of Literature

Introduction  Congenital absence of the aortic valve leaflets is a rare association with hypoplastic left heart syndrome (HLHS). Case  A 37-year-old pregnant woman was referred for fetal evaluation of possible HLHS at 22 weeks of gestation. The fetal echocardiogram (ECHO) was remarkable for a hypopl...

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Autores principales: Qasim, Amna, Johnson, Chelsea B., Aly, Muhammad A., Aly, Ashraf M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Medical Publishers 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6456327/
https://www.ncbi.nlm.nih.gov/pubmed/30972226
http://dx.doi.org/10.1055/s-0038-1677480
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author Qasim, Amna
Johnson, Chelsea B.
Aly, Muhammad A.
Aly, Ashraf M.
author_facet Qasim, Amna
Johnson, Chelsea B.
Aly, Muhammad A.
Aly, Ashraf M.
author_sort Qasim, Amna
collection PubMed
description Introduction  Congenital absence of the aortic valve leaflets is a rare association with hypoplastic left heart syndrome (HLHS). Case  A 37-year-old pregnant woman was referred for fetal evaluation of possible HLHS at 22 weeks of gestation. The fetal echocardiogram (ECHO) was remarkable for a hypoplastic left atrium, nearly atretic mitral valve, small left ventricle, and a hypoplastic aortic valve with severe aortic insufficiency. A female infant was born at term and postnatal ECHO confirmed the above findings. In addition, there was complete absence of the aortic valve leaflets. The patient underwent Norwood's procedure at day 5 of life with atrial septectomy, over-sewing of the aortic valve annulus, and a 4 mm Sano's shunt between the right ventricle and the main pulmonary artery. She tolerated this surgery well and subsequently underwent a bidirectional Glenn's procedure at 8 months of life. Conclusion  Prenatal diagnosis of absent aortic valve should be suspected in the presence of severe aortic insufficiency in the fetal ECHO. Early postnatal intervention is critical as those patients are likely to deteriorate quickly. The over-sewing of the aortic valve may be important to prevent coronary steal and myocardial hypoperfusion which could potentially be detrimental.
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spelling pubmed-64563272019-04-10 Prenatal Diagnosis and Successful Palliation of Absent Aortic Valve with Hypoplastic Left Heart Syndrome: A Case Report and Review of Literature Qasim, Amna Johnson, Chelsea B. Aly, Muhammad A. Aly, Ashraf M. AJP Rep Introduction  Congenital absence of the aortic valve leaflets is a rare association with hypoplastic left heart syndrome (HLHS). Case  A 37-year-old pregnant woman was referred for fetal evaluation of possible HLHS at 22 weeks of gestation. The fetal echocardiogram (ECHO) was remarkable for a hypoplastic left atrium, nearly atretic mitral valve, small left ventricle, and a hypoplastic aortic valve with severe aortic insufficiency. A female infant was born at term and postnatal ECHO confirmed the above findings. In addition, there was complete absence of the aortic valve leaflets. The patient underwent Norwood's procedure at day 5 of life with atrial septectomy, over-sewing of the aortic valve annulus, and a 4 mm Sano's shunt between the right ventricle and the main pulmonary artery. She tolerated this surgery well and subsequently underwent a bidirectional Glenn's procedure at 8 months of life. Conclusion  Prenatal diagnosis of absent aortic valve should be suspected in the presence of severe aortic insufficiency in the fetal ECHO. Early postnatal intervention is critical as those patients are likely to deteriorate quickly. The over-sewing of the aortic valve may be important to prevent coronary steal and myocardial hypoperfusion which could potentially be detrimental. Thieme Medical Publishers 2019-04 2019-04-09 /pmc/articles/PMC6456327/ /pubmed/30972226 http://dx.doi.org/10.1055/s-0038-1677480 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited.
spellingShingle Qasim, Amna
Johnson, Chelsea B.
Aly, Muhammad A.
Aly, Ashraf M.
Prenatal Diagnosis and Successful Palliation of Absent Aortic Valve with Hypoplastic Left Heart Syndrome: A Case Report and Review of Literature
title Prenatal Diagnosis and Successful Palliation of Absent Aortic Valve with Hypoplastic Left Heart Syndrome: A Case Report and Review of Literature
title_full Prenatal Diagnosis and Successful Palliation of Absent Aortic Valve with Hypoplastic Left Heart Syndrome: A Case Report and Review of Literature
title_fullStr Prenatal Diagnosis and Successful Palliation of Absent Aortic Valve with Hypoplastic Left Heart Syndrome: A Case Report and Review of Literature
title_full_unstemmed Prenatal Diagnosis and Successful Palliation of Absent Aortic Valve with Hypoplastic Left Heart Syndrome: A Case Report and Review of Literature
title_short Prenatal Diagnosis and Successful Palliation of Absent Aortic Valve with Hypoplastic Left Heart Syndrome: A Case Report and Review of Literature
title_sort prenatal diagnosis and successful palliation of absent aortic valve with hypoplastic left heart syndrome: a case report and review of literature
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6456327/
https://www.ncbi.nlm.nih.gov/pubmed/30972226
http://dx.doi.org/10.1055/s-0038-1677480
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