Sharma Tanya, Habash Fuad, Mounsey John, Baker Chris, Lopez Candales Angel
Internal Medicine, University of Arkansas for Medical Sciences, Little Rock, USA.
Cardiology, University of Arkansas for Medical Sciences, Little Rock, USA.
Cureus. 2020 Oct 2;12(10):e10773. doi: 10.7759/cureus.10773.
Ebstein's anomaly is a congenital defect, which is rarely present in adults with arrhythmias and right heart failure with tricuspid regurgitation. The diagnosis is made by non-invasive cardiac imaging with transthoracic echocardiography or cardiac magnetic resonance imaging. However, mild and atypical anatomical variants require a more specific investigation to make the diagnosis and differentiate it from other pathologies which have a similar presentation, including Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC). We present the case of a 66-year-old gentleman with a history of recurrent admissions due to decompensated heart failure exacerbations, now presenting with gradually worsening dyspnea. An echocardiogram was obtained, showing a thin-walled, dilated, and dysfunctional right ventricle (RV) with severe tricuspid regurgitation due to poor coaptation of the tricuspid leaflets. Although a very distinctive epsilon wave was seen on his electrocardiogram, highly suggestive of arrhythmogenic RV cardiomyopathy (ARVC), which would be enough to explain his presentation and initial echocardiogram; an off-axis plane of the tricuspid valve without any RV aneurysm or dilation of the RV outflow tract was incongruent with this diagnosis. Additional echocardiographic images were determinant to demonstrate both apical displacement and tethering of the septal tricuspid leaflet with an abnormally long anterior tricuspid leaflet, suggestive of Ebstein's anomaly. This diagnosis was confirmed with cardiac magnetic resonance imaging. Mild variants of Ebstein's anomaly, especially in the presence of confounding findings require focused imaging to ascertain the diagnosis. We review these non-traditional findings in trying to differentiate Ebstein's from ARVC.
埃布斯坦畸形是一种先天性缺陷,在患有心律失常、右心衰竭伴三尖瓣反流的成年人中很少见。通过经胸超声心动图或心脏磁共振成像等非侵入性心脏成像进行诊断。然而,轻度和非典型的解剖变异需要更具体的检查来进行诊断,并将其与其他表现相似的病理情况区分开来,包括致心律失常性右室心肌病(ARVC)。我们报告一例66岁男性患者,有因失代偿性心力衰竭加重而反复住院的病史,现出现逐渐加重的呼吸困难。进行了超声心动图检查,显示右心室壁薄、扩张且功能障碍,由于三尖瓣叶对合不良导致严重三尖瓣反流。尽管在他的心电图上看到了一个非常独特的ε波,高度提示致心律失常性右室心肌病(ARVC),这足以解释他的表现和最初的超声心动图结果;但三尖瓣的离轴平面且无任何右室动脉瘤或右室流出道扩张与该诊断不一致。额外的超声心动图图像对于显示间隔三尖瓣叶的尖部移位和附着以及异常长的前三尖瓣叶具有决定性作用,提示埃布斯坦畸形。心脏磁共振成像证实了这一诊断。埃布斯坦畸形的轻度变异,尤其是在存在混淆性发现的情况下,需要重点成像来确定诊断。我们回顾这些非传统发现,试图将埃布斯坦畸形与ARVC区分开来。