Literature DB >> 31654969

Progression of electrocardiographic changes in a patient with apical hypertrophic cardiomyopathy.

Rafael Harari1, Jeffrey Smietana1, John E Madias2.   

Abstract

A 58-year-old man asymptomatic from the cardiovascular point of view and with no known relevant family history was found by transthoracic echocardiography to have apical hypertrophic cardiomyopathy (AHCM). His electrocardiogram (ECG) revealed prominent precordial R-waves, particularly in V3-V4 leads, and "giant" (>1.0 mV), inverted T-waves, previously associated with AHCM. ECGs recorded 17 and 13 years previously, did not disclose such abnormalities, as the ones of his current ECG. The presented case illustrates a potential role of serial ECGs (along with serial imaging testing) in detecting the development and progression of regional left ventricular hypertrophy in patients with AHCM, and probably in other hypertrophic cardiomyopathy phenotypes.
Copyright © 2018. Published by Elsevier Inc.

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Mesh:

Year:  2019        PMID: 31654969     DOI: 10.1016/j.jelectrocard.2019.09.025

Source DB:  PubMed          Journal:  J Electrocardiol        ISSN: 0022-0736            Impact factor:   1.438


  1 in total

1.  Usefulness of ECG to differentiate apical hypertrophic cardiomyopathy from non-ST elevation acute coronary syndrome.

Authors:  Yirao Tao; Jing Xu; Samira Yerima Bako; Xiaobo Yao; Donghui Yang
Journal:  BMC Cardiovasc Disord       Date:  2020-06-23       Impact factor: 2.298

  1 in total

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