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A Constellation of Cardiac Anomalies: Beyond Shone's Complex

Shone's anomaly is a very rare congenital cardiac malformation characterized by four serial obstructive lesions of the left side of the heart (i) Supravalvular mitral membrane (ii) parachute mitral valve (iii) muscular or membranous subaortic stenosis and (iv) coarctation of aorta. We report a...

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Autores principales: Ganju, Neeraj K., Kandoria, Arvind, Thakur, Suresh, Ganju, Sunite A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4879801/
https://www.ncbi.nlm.nih.gov/pubmed/27293526
http://dx.doi.org/10.4103/1995-705X.182643
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author Ganju, Neeraj K.
Kandoria, Arvind
Thakur, Suresh
Ganju, Sunite A.
author_facet Ganju, Neeraj K.
Kandoria, Arvind
Thakur, Suresh
Ganju, Sunite A.
author_sort Ganju, Neeraj K.
collection PubMed
description Shone's anomaly is a very rare congenital cardiac malformation characterized by four serial obstructive lesions of the left side of the heart (i) Supravalvular mitral membrane (ii) parachute mitral valve (iii) muscular or membranous subaortic stenosis and (iv) coarctation of aorta. We report a unique presentation of Shone's complex in a 14-year-old adolescent male. In addition to the four characteristic lesions the patient had bicuspid aortic valve, aneurysm of sinus of valsalva, patent ductus arteriosus, ventricular septal defect, persistent left superior vena cava opening into coronary sinus and severe pulmonary artery hypertension. This case report highlights the importance of a strong clinical suspicion of the coexistence of multiple congenital cardiac anomalies in Shone's complex and the significance of a careful comprehensive echocardiography.
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spelling pubmed-48798012016-06-10 A Constellation of Cardiac Anomalies: Beyond Shone's Complex Ganju, Neeraj K. Kandoria, Arvind Thakur, Suresh Ganju, Sunite A. Heart Views Case Report Shone's anomaly is a very rare congenital cardiac malformation characterized by four serial obstructive lesions of the left side of the heart (i) Supravalvular mitral membrane (ii) parachute mitral valve (iii) muscular or membranous subaortic stenosis and (iv) coarctation of aorta. We report a unique presentation of Shone's complex in a 14-year-old adolescent male. In addition to the four characteristic lesions the patient had bicuspid aortic valve, aneurysm of sinus of valsalva, patent ductus arteriosus, ventricular septal defect, persistent left superior vena cava opening into coronary sinus and severe pulmonary artery hypertension. This case report highlights the importance of a strong clinical suspicion of the coexistence of multiple congenital cardiac anomalies in Shone's complex and the significance of a careful comprehensive echocardiography. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4879801/ /pubmed/27293526 http://dx.doi.org/10.4103/1995-705X.182643 Text en Copyright: © Heart Views 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-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Ganju, Neeraj K.
Kandoria, Arvind
Thakur, Suresh
Ganju, Sunite A.
A Constellation of Cardiac Anomalies: Beyond Shone's Complex
title A Constellation of Cardiac Anomalies: Beyond Shone's Complex
title_full A Constellation of Cardiac Anomalies: Beyond Shone's Complex
title_fullStr A Constellation of Cardiac Anomalies: Beyond Shone's Complex
title_full_unstemmed A Constellation of Cardiac Anomalies: Beyond Shone's Complex
title_short A Constellation of Cardiac Anomalies: Beyond Shone's Complex
title_sort constellation of cardiac anomalies: beyond shone's complex
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4879801/
https://www.ncbi.nlm.nih.gov/pubmed/27293526
http://dx.doi.org/10.4103/1995-705X.182643
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