梗阻性和非梗阻性肥厚性心肌病病例的副二尖瓣组织。

IF 0.6
İrem Türkmen, Arda Güler, Sezgin Atmaca, İffet Doğan, Gamze Babur Güler
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引用次数: 0

摘要

副二尖瓣组织(AMVT)是一种罕见的先天性心脏异常,通常与其他先天性心脏缺陷有关。通常在儿童期诊断,在成年期出现异常罕见,特别是在肥厚性心肌病(HCM)患者中。这两种情况的共存可使诊断复杂化,特别是在左心室流出道(LVOT)梯度形成的患者中。本病例系列强调了多模态成像在准确识别AMVT,将其与其他疾病区分开来以及确定AMVT的各种形态方面的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Accessory Mitral Valve Tissue in Both Obstructive and Nonobstructive Hypertrophic Cardiomyopathy Cases.

Accessory mitral valve tissue (AMVT) is a rare congenital cardiac anomaly often associated with other congenital heart defects. Typically diagnosed in childhood, its presence in adulthood is exceptionally rare, especially in patients with hypertrophic cardiomyopathy (HCM). The coexistence of these two conditions can complicate the diagnosis, particularly in patients with left ventricular outflow tract (LVOT) gradient formation. This case series highlights the importance of multimodal imaging in accurately identifying AMVT, differentiating it from other conditions, and determining the various morphologies of AMVT.

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