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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...

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Detalles Bibliográficos
Autores principales: Abugroun, Ashraf, Ahmed, Fatima, Vilchez, Daniel, Turaga, Lalita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2017
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.
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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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