Clinical Features and Management of Patients with an Anomalous Origin of the Coronary Arteries

Espejo-Paeres Carolina, O. Carmen, M. Pedro, I. Fabian, Higueras-Nafria Javier, V. David, Vilacosta Isidre
{"title":"Clinical Features and Management of Patients with an Anomalous Origin of the Coronary Arteries","authors":"Espejo-Paeres Carolina, O. Carmen, M. Pedro, I. Fabian, Higueras-Nafria Javier, V. David, Vilacosta Isidre","doi":"10.23937/iacvd-2017/1710005","DOIUrl":null,"url":null,"abstract":"Background: An anomalous origin of a coronary artery is a rare congenital condition in which a coronary artery arises from the opposite coronary sinus. Most coronary artery anomalies are an incidental finding without clinical signifi -cance, although some cases may be potentially life threat-ening, depending on the origin, course and termination of the anomalous vessel. Anatomical features of risk are an aortic intramural course or inter-arterial course. Methods: We present 4 cases of an anomalous origin of the coronary arteries with radiological confirmation by cardiac computed tomography angiography (CCTA) and clinical history of chest pain. Two patients were incidentally diagnosed by invasive coronary angiography, while two of them under-went a CCTA exam directly. Ischemia detection tests such as treadmill test or myocardial perfusion imaging with single photon emission computed tomography (SPECT) were performed in all of them to rule out ischemia. Results: In all 4 cases, none relationship between clinical symptoms and anatomical features was established. Once ischemia was ruled-out by ischemia detection tests, we chose clinical follow-up instead of surgery given the ab-sence of anatomical or risk clinical features. Conclusion: Only a minority of patients have symptoms due to these coronary anomalies. An expectant attitude with periodical surveillance seems to be the best option in patients with low-risk variants of coronary artery anomalies without clinical documentation of myocardial ischemia.","PeriodicalId":170730,"journal":{"name":"International Archives of Cardiovascular Diseases","volume":"41 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Archives of Cardiovascular Diseases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.23937/iacvd-2017/1710005","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

Background: An anomalous origin of a coronary artery is a rare congenital condition in which a coronary artery arises from the opposite coronary sinus. Most coronary artery anomalies are an incidental finding without clinical signifi -cance, although some cases may be potentially life threat-ening, depending on the origin, course and termination of the anomalous vessel. Anatomical features of risk are an aortic intramural course or inter-arterial course. Methods: We present 4 cases of an anomalous origin of the coronary arteries with radiological confirmation by cardiac computed tomography angiography (CCTA) and clinical history of chest pain. Two patients were incidentally diagnosed by invasive coronary angiography, while two of them under-went a CCTA exam directly. Ischemia detection tests such as treadmill test or myocardial perfusion imaging with single photon emission computed tomography (SPECT) were performed in all of them to rule out ischemia. Results: In all 4 cases, none relationship between clinical symptoms and anatomical features was established. Once ischemia was ruled-out by ischemia detection tests, we chose clinical follow-up instead of surgery given the ab-sence of anatomical or risk clinical features. Conclusion: Only a minority of patients have symptoms due to these coronary anomalies. An expectant attitude with periodical surveillance seems to be the best option in patients with low-risk variants of coronary artery anomalies without clinical documentation of myocardial ischemia.
冠状动脉起源异常患者的临床特点和处理
背景:冠状动脉异常起源是一种罕见的先天性疾病,其中冠状动脉起源于对侧冠状窦。大多数冠状动脉异常是偶然发现的,没有临床意义,尽管一些病例可能会危及生命,这取决于异常血管的起源、过程和终止。危险的解剖特征是主动脉壁内径或动脉间径。方法:我们报告了4例冠状动脉起源异常的病例,并通过心脏计算机断层血管造影(CCTA)和胸痛的临床病史进行了放射学证实。2例患者通过有创冠状动脉造影偶然诊断,2例患者直接行CCTA检查。所有患者均行缺血检测试验,如跑步机试验或单光子发射计算机断层扫描(SPECT)心肌灌注成像,以排除缺血。结果:4例患者的临床症状与解剖特征均无相关性。一旦通过缺血检测测试排除缺血,我们选择临床随访而不是手术,因为没有解剖或危险的临床特征。结论:只有少数患者有冠状动脉异常引起的症状。对于无心肌缺血临床记录的低风险冠状动脉异常变异体患者,定期监测的期待态度似乎是最好的选择。
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 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信