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年轻竞技运动员中伴有家族性肥厚型心肌病的可逆性心尖肥厚。

Reversible Apical Hypertrophy in a Young Competitive Athlete with Familiar Hypertrophic Cardiomyopathy.

机构信息

Department of Cardiology and Sport Medicine, Institute of Sport Medicine and Science, National Italian Olympic Committee, Rome, Italy.

Department of Cardiovascular Sciences, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.

出版信息

Am J Case Rep. 2023 Apr 8;24:e939058. doi: 10.12659/AJCR.939058.

Abstract

BACKGROUND Differential diagnosis between athlete's heart and hypertrophic cardiomyopathy is sometimes challenging in sport cardiology since endurance training can cause a distinct pattern of functional and structural changes of the cardiovascular system. It is of crucial importance to accurately diagnose it and stratify the arrhythmic risk since hypertrophic cardiomyopathy is one of the leading causes of sudden cardiac death in young athletes. Apical hypertrophic cardiomyopathy is a relatively rare form of hypertrophic cardiomyopathy that predominantly affects the apex of the left ventricle and usually has a nonobstructive physiology. Few data and studies are available on influence of aerobic training (and detraining) on morphological changes in athletes with apical hypertrophic cardiomyopathy. CASE REPORT We present the case of a 19-year-old male soccer athlete with family history for obstructive hypertrophic cardiomyopathy, with electrocardiographic and morphological left ventricular remodeling in association with sports activity. Intensive aerobic training led to marked T-wave inversion on 12-lead ECG and left ventricular hypertrophy compatible with apical hypertrophic cardiomyopathy. Genetic testing confirmed the presence of familial variant c853C>T, p.(Arg 285Cys) on TNNT2 gene. After 18 months detraining, we observed a complete regression of ECG abnormalities and a reverse remodeling of the left ventricular hypertrophy. No pharmacological therapy was indicated; periodic cardiological evaluations were advised. Monitoring devices or implantable cardioverter defibrillator were not recommended. CONCLUSIONS This case suggests that intensive aerobic training can affect the pathological hypertrophic cardiomyopathy substrate, facilitating the development of left ventricular hypertrophy and, more interesting, regression of structural changes after detraining.

摘要

背景

在运动心脏病学中,运动员心脏与肥厚型心肌病的鉴别诊断有时具有挑战性,因为耐力训练会导致心血管系统出现明显的功能和结构变化。准确诊断并分层心律失常风险至关重要,因为肥厚型心肌病是年轻运动员心源性猝死的主要原因之一。心尖肥厚型心肌病是一种相对罕见的肥厚型心肌病,主要影响左心室心尖,通常具有非梗阻性生理学。关于有氧运动(和停训)对心尖肥厚型心肌病运动员形态变化的影响,仅有少量数据和研究。

病例报告

我们报告了一例 19 岁男性足球运动员,有梗阻性肥厚型心肌病家族史,伴有心电图和左心室形态重构,与运动活动有关。剧烈的有氧运动导致 12 导联心电图出现明显的 T 波倒置和左心室肥厚,符合心尖肥厚型心肌病。基因检测证实存在 TNNT2 基因上的家族变体 c853C>T,p.(Arg 285Cys)。停训 18 个月后,我们观察到心电图异常完全消退,左心室肥厚逆转。未指示药物治疗;建议定期进行心脏评估。未推荐监测设备或植入式心脏复律除颤器。

结论

本病例提示,剧烈的有氧运动可能会影响病理性肥厚型心肌病的基质,促进左心室肥厚的发展,更有趣的是,停训后结构变化会逆转。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9bb/10091469/d8f1873ef273/amjcaserep-24-e939058-g001.jpg

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