The Role of Computed Tomography in The Diagnosis of Rare Congenital Heart Disease: Interrupted Aortic Arch.

Yu Feng, Lijuan Wang, Hui Liu, Guifang Sun, Bin Liu, Pengcheng Ma, Liqiong Wang, Xuguang Zhang
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Abstract

Interrupted aortic arch (IAA) is a rare congenital anomaly of the aortic arch and an anatomical interruption of the lumen between the ascending and descending aorta. Computed tomography (CT) has become a reliable noninvasive diagnostic method for congenital IAA. The purpose of this study was to investigate the imaging features of IAA and improve the understanding and diagnosis of the disease. The imaging features and postoperative pathological data of 25 patients with IAA confirmed by dual-source computed tomography (DSCT) angiography were analyzed in this retrospective study. Among the 25 patients with IAA, 15 were type A, seven were type B, 0 were types C and D, and two were type E. The diameter of the pulmonary artery trunk in type A was larger than that in type B (P < 0.05). However, there were no significant differences between types A and B along the ascending aorta diameter, descending aorta, ascending aorta/descending aorta ratio, left pulmonary artery main trunk diameter, right pulmonary artery main trunk diameter, left pulmonary artery trunk/pulmonary artery trunk ratio, right pulmonary artery trunk/pulmonary artery trunk ratio, and left pulmonary artery trunk/right pulmonary artery trunk ratio. The imaging findings of IAA have typical and specific signs, and the types of IAA are not comprehensive. One type of patient identification can be added: Patients who are dissected between the left common carotid artery and left subclavian artery opening, and the descending aorta is circulated by the chest collaterals. Patients with a wide pulmonary artery in the IAA are usually type A patients. Patients with IAA after surgical repair require lifetime follow up, mainly to monitor left ventricular outflow tract obstruction and recurrent aortic coarctation. This study was approved by the Ethics Committee of Kunming Yan'an Hospital (Kunming City, Yunnan Province, China), and consent was waived because of the retrospective data collection.
计算机断层扫描在罕见先天性心脏病诊断中的作用:主动脉弓中断。
主动脉弓中断(IAA)是一种罕见的先天性主动脉弓异常,是升降主动脉间管腔的解剖中断。计算机断层扫描(CT)已成为一种可靠的无创诊断先天性IAA的方法。本研究旨在探讨IAA的影像学特征,提高对该病的认识和诊断。回顾性分析25例经DSCT血管造影证实的IAA患者的影像学特点及术后病理资料。25例IAA患者中,A型15例,B型7例,C、D型0例,e型2例。A型肺动脉干直径大于B型(P < 0.05)。A型与B型在升主动脉直径、降主动脉、升主动脉/降主动脉比值、左肺动脉主干直径、右肺动脉主干直径、左肺动脉主干/肺动脉主干比值、右肺动脉主干/肺动脉主干比值、左肺动脉主干/右肺动脉主干比值等指标上无显著差异。IAA的影像学表现具有典型性和特异性,且类型不全面。可增加一种患者识别类型:解剖于左侧颈总动脉与左侧锁骨下动脉开口之间,降主动脉经胸侧支循环的患者。IAA区肺动脉宽的患者通常为a型患者。术后IAA患者需终身随访,主要监测左心室流出道梗阻及主动脉瓣再发性缩窄。本研究经中国云南省昆明市延安医院伦理委员会批准,并因回顾性数据收集而放弃同意。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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