A Rare Case with Dissection of Pulmonary and Aorta in Aortopulmonary Window

A. Amin, Mozhgan Parsaee, Homa Ghaderian, Fatemeh Zohrian, A. Mohamadifar
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引用次数: 0

Abstract

Aortopulmonary window is a rare congenital anomaly which is commonly associated with other lesions such as patent ductus arteriosus, interrupted aortic arch, Atrial Septal Defect (ASD), and Ventricular Septal Defect (VSD). Aortic aneurysm and dissection have not been reported as an associated anomaly in AP window. A 44 -year-old male, with inoperable AortoPulmonary Window (AP window) and Eisenmenger syndrome presented to our Emergency Department with back pain and shortness of breath. Transthoracic echocardiography and aortic CT angiography depicted aneurysmal dilatation of ascending aorta with a dissection flap which was extended to main pulmonary artery. Any intervention was very high risk, due to the risk of imminent RV failure. The patient was hemodynamically stable and the symptoms seemed to be chronic, so we decided to manage him medically. AP window is a rare congenital anomaly which is commonly associated with other anomalies. In this report, we represent a rare case of AP window and Eisenmenger syndrome with aortic aneurysm and dissecting flap in ascending aorta and pulmonary artery who was managed medically.
肺动脉窗肺主动脉夹层1例
主动脉肺窗是一种罕见的先天性异常,通常与其他病变如动脉导管未闭、主动脉弓中断、房间隔缺损(ASD)和室间隔缺损(VSD)有关。主动脉动脉瘤和夹层并没有作为AP窗相关异常的报道。一名44岁男性,患有不能手术的主动脉肺窗(AP窗)和艾森曼格综合征,因背部疼痛和呼吸短促而就诊于急诊科。经胸超声心动图及主动脉CT血管造影显示升主动脉动脉瘤样扩张,夹层皮瓣延伸至肺动脉主干。任何干预都是非常高的风险,因为有可能发生右心室衰竭。病人血流动力学稳定,症状似乎是慢性的,所以我们决定对他进行医学治疗。AP窗是一种罕见的先天性异常,通常与其他异常相关。在本报告中,我们报告了一例罕见的AP窗和Eisenmenger综合征合并升主动脉和肺动脉动脉瘤和夹层皮瓣的病例,并对其进行了医学治疗。
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