Department of Cardiovascular Radiology & Endovascular Interventions, All India Institute of Medical Sciences, New Delhi, India.
Department of Cardiology, All India Institute of Medical Sciences, New Delhi, India.
J Card Surg. 2022 Jul;37(7):1928-1936. doi: 10.1111/jocs.16468. Epub 2022 Apr 8.
The present study sought to study the imaging associations of left atrioventricular valve (mitral) atresia and patent aortic root in patients with isomerism of atrial appendages as detected on multidetector computed tomography (CT) angiography MATERIALS AND METHODS: The CT angiography studies performed at a tertiary medical center from January 2014 to December 2021 were retrospectively evaluated to identify patients with left atrioventricular valve atresia and patent aortic root with isometric atrial chambers. The morphology of the atrial appendage and extent of pectinate muscles was used to identify the type of isomeric atrial chambers. A comprehensive assessment of discordant arrangement of organs and the variations in venoatrial connections was done.
Left atrioventricular valve atresia in the presence of patent aortic root and isomeric atrial appendages was identified in eight patients (four males). The mean age at diagnosis was 7 years. Right isomerism of the atrial appendages was seen in five patients while three patients had left isomerism. Disharmonious patterns of abdominal visceral arrangement were seen in two patients. Atrial and ventricular septal defects were seen in all patients. The most common pattern of ventricular arterial connection was DORV (double outlet right ventricle) (n = 4). While five patients had normally related great arteries, three had aorta anterior to the pulmonary trunk. Right ventricular outflow obstruction was seen in seven patients. Right aortic arch with mirror image branching was seen in four patients. Coronary artery anomalies were seen in four patients.
The presence of left atrioventricular valve atresia and patent aortic root with isomeric atrial appendages is a rare congenital anomaly frequently associated with anomalous systemic and pulmonary drainage, conotruncal anomalies, and right ventricular outflow obstruction. Hence, comprehensive CT-based evaluation is indispensable in providing detailed anatomy and aids in presurgical planning.
本研究旨在通过多排 CT 血管造影(CTA)研究,探讨心房附器异构患者中左房室瓣(二尖瓣)闭锁和升主动脉开放之间的影像学关联。
回顾性分析 2014 年 1 月至 2021 年 12 月在三级医疗中心进行的 CTA 研究,以确定存在左房室瓣闭锁和升主动脉开放伴等大心房的患者。使用心房附器的形态和梳状肌的范围来识别异构心房的类型。对器官的不一致排列和静脉心房连接的变异进行全面评估。
在 8 例(男 4 例)患者中发现了左房室瓣闭锁、升主动脉开放和异构心房附器。诊断时的平均年龄为 7 岁。5 例患者右心房附器异构,3 例患者左心房附器异构。2 例患者存在腹部内脏排列不协调的模式。所有患者均存在房间隔和室间隔缺损。最常见的心室动脉连接模式为 DORV(右心室双出口)(n=4)。5 例患者大动脉正常相关,3 例患者主动脉位于肺动脉干之前。7 例患者存在右心室流出道梗阻。4 例患者存在右主动脉弓伴镜像分支。4 例患者存在冠状动脉异常。
左房室瓣闭锁和升主动脉开放伴异构心房附器是一种罕见的先天性异常,常伴有异常的体循环和肺循环引流、圆锥动脉干异常和右心室流出道梗阻。因此,基于 CT 的全面评估对于提供详细的解剖结构和辅助术前规划是必不可少的。