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A case of mid-apical obstructive hypertrophic cardiomyopathy treated with a transapical myectomy approach: a case report
INTRODUCTION: Hypertrophic cardiomyopathy is a genetic cardiac disease characterized by marked variability in morphological expression and natural history. The hypertrophic myocardium is often confined to the septum or lateral wall of the left ventricle, but it can also be encountered in the middle...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4232228/ https://www.ncbi.nlm.nih.gov/pubmed/25384531 http://dx.doi.org/10.1186/1752-1947-8-364 |
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author | Scudeler, Thiago Luis Rezende, Paulo Cury Oikawa, Fernando Teiichi Costa da Costa, Leandro Menezes Alves Hueb, Alexandre Ciappina Hueb, Whady |
author_facet | Scudeler, Thiago Luis Rezende, Paulo Cury Oikawa, Fernando Teiichi Costa da Costa, Leandro Menezes Alves Hueb, Alexandre Ciappina Hueb, Whady |
author_sort | Scudeler, Thiago Luis |
collection | PubMed |
description | INTRODUCTION: Hypertrophic cardiomyopathy is a genetic cardiac disease characterized by marked variability in morphological expression and natural history. The hypertrophic myocardium is often confined to the septum or lateral wall of the left ventricle, but it can also be encountered in the middle or apical segments of the myocardium. Treatment is based on medical therapy. Others therapies, such as embolization of the septal artery or ventriculomyectomy, are indicated in special situations. Surgery is the standard treatment, and it is classically done via a transaortic approach; however, in cases in which the hypertrophic myocardium is confined to mid-apical segments, a transapical approach is an option. Only a few cases of mid-apical obstructive hypertrophic cardiomyopathy treated with a myectomy using a transapical approach have been reported in the English-language literature. In this report, we present a case of a patient with mid-apical obstructive hypertrophic cardiomyopathy treated using this new approach. CASE PRESENTATION: A 63-year-old Caucasian woman presented with a history of chest pain and shortness of breath causing significant limitations on her daily life activities. She had a history of coronary artery disease. Her physical examination was unremarkable. Transthoracic echocardiography revealed normal systolic function and significant concentric left ventricular hypertrophy that was greater in the mid-apical region. Nuclear magnetic resonance imaging confirmed significant hypertrophy of the median segments of the left ventricle. The patient had persistent symptoms despite receiving optimized medical treatment, and a surgical approach was indicated. As a myectomy using transaortic technique was thought to be difficult to perform in her case, a transapical approach was used. No complications occurred, and her symptoms resolved. CONCLUSION: A transapical myectomy should be taken into consideration for patients with mid-apical obstructive hypertrophic cardiomyopathy that is refractory to medical treatment. |
format | Online Article Text |
id | pubmed-4232228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42322282014-11-15 A case of mid-apical obstructive hypertrophic cardiomyopathy treated with a transapical myectomy approach: a case report Scudeler, Thiago Luis Rezende, Paulo Cury Oikawa, Fernando Teiichi Costa da Costa, Leandro Menezes Alves Hueb, Alexandre Ciappina Hueb, Whady J Med Case Rep Case Report INTRODUCTION: Hypertrophic cardiomyopathy is a genetic cardiac disease characterized by marked variability in morphological expression and natural history. The hypertrophic myocardium is often confined to the septum or lateral wall of the left ventricle, but it can also be encountered in the middle or apical segments of the myocardium. Treatment is based on medical therapy. Others therapies, such as embolization of the septal artery or ventriculomyectomy, are indicated in special situations. Surgery is the standard treatment, and it is classically done via a transaortic approach; however, in cases in which the hypertrophic myocardium is confined to mid-apical segments, a transapical approach is an option. Only a few cases of mid-apical obstructive hypertrophic cardiomyopathy treated with a myectomy using a transapical approach have been reported in the English-language literature. In this report, we present a case of a patient with mid-apical obstructive hypertrophic cardiomyopathy treated using this new approach. CASE PRESENTATION: A 63-year-old Caucasian woman presented with a history of chest pain and shortness of breath causing significant limitations on her daily life activities. She had a history of coronary artery disease. Her physical examination was unremarkable. Transthoracic echocardiography revealed normal systolic function and significant concentric left ventricular hypertrophy that was greater in the mid-apical region. Nuclear magnetic resonance imaging confirmed significant hypertrophy of the median segments of the left ventricle. The patient had persistent symptoms despite receiving optimized medical treatment, and a surgical approach was indicated. As a myectomy using transaortic technique was thought to be difficult to perform in her case, a transapical approach was used. No complications occurred, and her symptoms resolved. CONCLUSION: A transapical myectomy should be taken into consideration for patients with mid-apical obstructive hypertrophic cardiomyopathy that is refractory to medical treatment. BioMed Central 2014-11-11 /pmc/articles/PMC4232228/ /pubmed/25384531 http://dx.doi.org/10.1186/1752-1947-8-364 Text en Copyright © 2014 Scudeler et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Scudeler, Thiago Luis Rezende, Paulo Cury Oikawa, Fernando Teiichi Costa da Costa, Leandro Menezes Alves Hueb, Alexandre Ciappina Hueb, Whady A case of mid-apical obstructive hypertrophic cardiomyopathy treated with a transapical myectomy approach: a case report |
title | A case of mid-apical obstructive hypertrophic cardiomyopathy treated with a transapical myectomy approach: a case report |
title_full | A case of mid-apical obstructive hypertrophic cardiomyopathy treated with a transapical myectomy approach: a case report |
title_fullStr | A case of mid-apical obstructive hypertrophic cardiomyopathy treated with a transapical myectomy approach: a case report |
title_full_unstemmed | A case of mid-apical obstructive hypertrophic cardiomyopathy treated with a transapical myectomy approach: a case report |
title_short | A case of mid-apical obstructive hypertrophic cardiomyopathy treated with a transapical myectomy approach: a case report |
title_sort | case of mid-apical obstructive hypertrophic cardiomyopathy treated with a transapical myectomy approach: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4232228/ https://www.ncbi.nlm.nih.gov/pubmed/25384531 http://dx.doi.org/10.1186/1752-1947-8-364 |
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