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Apical hypertrophic cardiomyopathy: diagnosis, medical and surgical treatment

Apical hypertrophic cardiomyopathy (AHCM) is a rare form of hypertrophic cardiomyopathy, occasionally resulting in severe complications. The paper covers the etiology and pathogenesis of AHCM, different imaging methods and characteristic appearance of the disease in each of them. Echocardiography an...

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Autores principales: Paluszkiewicz, Jerzy, Krasinska, Beata, Milting, Hendrik, Gummert, Jan, Pyda, Małgorzata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329883/
https://www.ncbi.nlm.nih.gov/pubmed/30647749
http://dx.doi.org/10.5114/kitp.2018.80922
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author Paluszkiewicz, Jerzy
Krasinska, Beata
Milting, Hendrik
Gummert, Jan
Pyda, Małgorzata
author_facet Paluszkiewicz, Jerzy
Krasinska, Beata
Milting, Hendrik
Gummert, Jan
Pyda, Małgorzata
author_sort Paluszkiewicz, Jerzy
collection PubMed
description Apical hypertrophic cardiomyopathy (AHCM) is a rare form of hypertrophic cardiomyopathy, occasionally resulting in severe complications. The paper covers the etiology and pathogenesis of AHCM, different imaging methods and characteristic appearance of the disease in each of them. Echocardiography and cardiovascular magnetic resonance imaging (CMR) are known to be the most valuable imaging methods. Moreover, this review presents medical and surgical treatment, as well as the clinical course and prognosis. Despite possible morbid events the overall cardiovascular mortality rate of AHCM patients is low, and the prognosis is relatively optimistic.
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spelling pubmed-63298832019-01-15 Apical hypertrophic cardiomyopathy: diagnosis, medical and surgical treatment Paluszkiewicz, Jerzy Krasinska, Beata Milting, Hendrik Gummert, Jan Pyda, Małgorzata Kardiochir Torakochirurgia Pol Review Paper Apical hypertrophic cardiomyopathy (AHCM) is a rare form of hypertrophic cardiomyopathy, occasionally resulting in severe complications. The paper covers the etiology and pathogenesis of AHCM, different imaging methods and characteristic appearance of the disease in each of them. Echocardiography and cardiovascular magnetic resonance imaging (CMR) are known to be the most valuable imaging methods. Moreover, this review presents medical and surgical treatment, as well as the clinical course and prognosis. Despite possible morbid events the overall cardiovascular mortality rate of AHCM patients is low, and the prognosis is relatively optimistic. Termedia Publishing House 2018-12-31 2018-12 /pmc/articles/PMC6329883/ /pubmed/30647749 http://dx.doi.org/10.5114/kitp.2018.80922 Text en Copyright: © 2018 Polish Society of Cardiothoracic Surgeons (Polskie Towarzystwo KardioTorakochirurgów) and the editors of the Polish Journal of Cardio-Thoracic Surgery (Kardiochirurgia i Torakochirurgia Polska) http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Review Paper
Paluszkiewicz, Jerzy
Krasinska, Beata
Milting, Hendrik
Gummert, Jan
Pyda, Małgorzata
Apical hypertrophic cardiomyopathy: diagnosis, medical and surgical treatment
title Apical hypertrophic cardiomyopathy: diagnosis, medical and surgical treatment
title_full Apical hypertrophic cardiomyopathy: diagnosis, medical and surgical treatment
title_fullStr Apical hypertrophic cardiomyopathy: diagnosis, medical and surgical treatment
title_full_unstemmed Apical hypertrophic cardiomyopathy: diagnosis, medical and surgical treatment
title_short Apical hypertrophic cardiomyopathy: diagnosis, medical and surgical treatment
title_sort apical hypertrophic cardiomyopathy: diagnosis, medical and surgical treatment
topic Review Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329883/
https://www.ncbi.nlm.nih.gov/pubmed/30647749
http://dx.doi.org/10.5114/kitp.2018.80922
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AT gummertjan apicalhypertrophiccardiomyopathydiagnosismedicalandsurgicaltreatment
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