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Apical Hypertrophic Cardiomyopathy: A Case Report
Apical hypertrophic cardiomyopathy (ApHCM) is a rare variant of hypertrophic cardiomyopathy, characterized by a spade-like left ventricular cavity. A 58-year-old African-American female with past medical history of hypertension presented for evaluation of recurrent exertional chest tightness, palpit...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elmer Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5667717/ https://www.ncbi.nlm.nih.gov/pubmed/29118892 http://dx.doi.org/10.14740/cr619w |
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author | Abugroun, Ashraf Ahmed, Fatima Vilchez, Daniel Turaga, Lalita |
author_facet | Abugroun, Ashraf Ahmed, Fatima Vilchez, Daniel Turaga, Lalita |
author_sort | Abugroun, Ashraf |
collection | PubMed |
description | Apical hypertrophic cardiomyopathy (ApHCM) is a rare variant of hypertrophic cardiomyopathy, characterized by a spade-like left ventricular cavity. A 58-year-old African-American female with past medical history of hypertension presented for evaluation of recurrent exertional chest tightness, palpitations and headache. Prior workup including multiple stress tests and angiogram was non-conclusive. Electrocardiogram (EKG) showed characteristic marked T-waves inversions in inferior leads and left ventriculography revealed left ventricle apical hypertrophy with spade like left ventricular cavity that was typical of Yamaguchi syndrome. This case highlights the rare incidence of the disease among African American as well as the challenging diagnostic and presentation features of the disease. |
format | Online Article Text |
id | pubmed-5667717 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elmer Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56677172017-11-08 Apical Hypertrophic Cardiomyopathy: A Case Report Abugroun, Ashraf Ahmed, Fatima Vilchez, Daniel Turaga, Lalita Cardiol Res Case Report Apical hypertrophic cardiomyopathy (ApHCM) is a rare variant of hypertrophic cardiomyopathy, characterized by a spade-like left ventricular cavity. A 58-year-old African-American female with past medical history of hypertension presented for evaluation of recurrent exertional chest tightness, palpitations and headache. Prior workup including multiple stress tests and angiogram was non-conclusive. Electrocardiogram (EKG) showed characteristic marked T-waves inversions in inferior leads and left ventriculography revealed left ventricle apical hypertrophy with spade like left ventricular cavity that was typical of Yamaguchi syndrome. This case highlights the rare incidence of the disease among African American as well as the challenging diagnostic and presentation features of the disease. Elmer Press 2017-10 2017-10-27 /pmc/articles/PMC5667717/ /pubmed/29118892 http://dx.doi.org/10.14740/cr619w Text en Copyright 2017, Abugroun et al. http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Non-Commercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Abugroun, Ashraf Ahmed, Fatima Vilchez, Daniel Turaga, Lalita Apical Hypertrophic Cardiomyopathy: A Case Report |
title | Apical Hypertrophic Cardiomyopathy: A Case Report |
title_full | Apical Hypertrophic Cardiomyopathy: A Case Report |
title_fullStr | Apical Hypertrophic Cardiomyopathy: A Case Report |
title_full_unstemmed | Apical Hypertrophic Cardiomyopathy: A Case Report |
title_short | Apical Hypertrophic Cardiomyopathy: A Case Report |
title_sort | apical hypertrophic cardiomyopathy: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5667717/ https://www.ncbi.nlm.nih.gov/pubmed/29118892 http://dx.doi.org/10.14740/cr619w |
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