中室性肥厚性心肌病伴顶动脉瘤:多模态影像学病例报告。

Pavel Martinez-Dominguez, Manuel Horna-Noriega, María José Santa-Ana-Bayona, Sara Ramírez-Flores, Lucia Horna-Regalado, Nilda Espinola-Zavaleta
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引用次数: 0

摘要

中室性肥厚性心肌病是肥厚性心肌病中一个罕见的亚组,它可能表现为顶端动脉瘤。这种情况与心脏不良事件的风险增加有关,包括心脏骤停、心力衰竭、血栓栓塞事件或心源性猝死。我们提出的情况下,一个41岁的男子谁提出的历史,用力呼吸困难和晕厥。超声心动图和心脏磁共振多模态成像显示心室中段肥大并伴有顶端动脉瘤。植入可植入式心脏转复除颤器以防止心源性猝死。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mid-ventricular hypertrophic cardiomyopathy with apical aneurysm: a multimodality imaging case report.

Mid-ventricular hypertrophic cardiomyopathy is a rare subgroup within hypertrophic cardiomyopathies that may present with apical aneurysm. This condition is associated with an increased risk of cardiac adverse events, including cardiac arrest, heart failure, thromboembolic events, or sudden cardiac death. We present a case of a 41-year-old man who presented with a history of exertional dyspnea and syncope. Multimodality imaging with echocardiography and cardiac magnetic resonance showed hypertrophy of the mid-ventricular segments with apical aneurysm. An implantable cardioverter-defibrillator was implanted to prevent sudden cardiac death.

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