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

A. Amin, Mozhgan Parsaee, Homa Ghaderian, Fatemeh Zohrian, A. Mohamadifar
{"title":"A Rare Case with Dissection of Pulmonary and Aorta in Aortopulmonary Window","authors":"A. Amin, Mozhgan Parsaee, Homa Ghaderian, Fatemeh Zohrian, A. Mohamadifar","doi":"10.18502/crcp.v7i4.11599","DOIUrl":null,"url":null,"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.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Clinical Practice","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18502/crcp.v7i4.11599","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
43
审稿时长
12 weeks
期刊最新文献
Adult Presentation of Meckel’s Diverticulum: A Case Report Adhesion Band Small Bowel Obstruction in Virgin Abdomen: A Case Report A Colorectal Adenocarcinoma With Obstruction in a 26-Year-Old Man: A Case Report in an Unlikely Age Group Occult Pheochromocytoma and Acute Ischaemic Stroke in Young Adult: Cause or Association Presentation Invasive Mole After Normal Pregnancy: A Very Rare Case Report
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1