[Coronary embolism from atrial myxoma: a rare cause of myocardial infarction? Case report and literature review].

IF 1.5 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
Gianmaria Scherillo, Enrico Cerrato, Stefania Ferrua, Ilaria Meynet, Marco Lococo, Paolo Calabrò, Mauro Rinaldi, Ferdinando Varbella
{"title":"[Coronary embolism from atrial myxoma: a rare cause of myocardial infarction? Case report and literature review].","authors":"Gianmaria Scherillo, Enrico Cerrato, Stefania Ferrua, Ilaria Meynet, Marco Lococo, Paolo Calabrò, Mauro Rinaldi, Ferdinando Varbella","doi":"10.1714/4651.46656","DOIUrl":null,"url":null,"abstract":"<p><p>A 44-year-old man with no known cardiovascular history or risk factors experienced chest pain after a volleyball match. ECG showed ST-segment elevation in the inferior leads, a finding consistent with ST-elevation myocardial infarction (STEMI). The patient was urgently taken to the cath lab, where coronary angiography revealed complete occlusion of the distal left anterior descending artery and of an obtuse marginal branch. Plain old balloon angioplasty was attempted but unsuccessful. During the procedure, an abnormal vascular network originating from the right coronary artery and the circumflex artery and directed toward the left atrium was observed. Transthoracic echocardiography revealed a 30 x 32 mm ovoid, pedunculated mass attached to the atrial roof. Transesophageal echocardiography confirmed the finding, very suggestive of an atrial myxoma. Upon deeper anamnesis, the patient reported transient episodes of visual loss. Brain magnetic resonance imaging revealed multiple small gliotic lesions, indicative of systemic embolization. The patient underwent surgical resection of the mass via right mini-thoracotomy. Histological analysis confirmed the diagnosis of atrial myxoma. This case highlights the importance of considering an embolic etiology in STEMI, especially in young patients without traditional cardiovascular risk factors.</p>","PeriodicalId":12510,"journal":{"name":"Giornale italiano di cardiologia","volume":"27 3 Suppl. 1","pages":"6S-10S"},"PeriodicalIF":1.5000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Giornale italiano di cardiologia","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1714/4651.46656","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0

Abstract

A 44-year-old man with no known cardiovascular history or risk factors experienced chest pain after a volleyball match. ECG showed ST-segment elevation in the inferior leads, a finding consistent with ST-elevation myocardial infarction (STEMI). The patient was urgently taken to the cath lab, where coronary angiography revealed complete occlusion of the distal left anterior descending artery and of an obtuse marginal branch. Plain old balloon angioplasty was attempted but unsuccessful. During the procedure, an abnormal vascular network originating from the right coronary artery and the circumflex artery and directed toward the left atrium was observed. Transthoracic echocardiography revealed a 30 x 32 mm ovoid, pedunculated mass attached to the atrial roof. Transesophageal echocardiography confirmed the finding, very suggestive of an atrial myxoma. Upon deeper anamnesis, the patient reported transient episodes of visual loss. Brain magnetic resonance imaging revealed multiple small gliotic lesions, indicative of systemic embolization. The patient underwent surgical resection of the mass via right mini-thoracotomy. Histological analysis confirmed the diagnosis of atrial myxoma. This case highlights the importance of considering an embolic etiology in STEMI, especially in young patients without traditional cardiovascular risk factors.

心房黏液瘤所致冠状动脉栓塞:心肌梗死的罕见病因?病例报告及文献复习]。
一名44岁男性,无已知心血管病史或危险因素,在排球比赛后出现胸痛。心电图显示下导联st段抬高,与st段抬高型心肌梗死(STEMI)一致。患者被紧急送往导管实验室,冠状动脉造影显示左前降支远端完全闭塞,边缘支钝化。尝试了普通的球囊血管成形术,但没有成功。在手术过程中,观察到一个异常的血管网络起源于右冠状动脉和旋动脉,并指向左心房。经胸超声心动图显示一个30 × 32毫米的卵形带梗肿块附着于房顶。经食管超声心动图证实了这一发现,非常提示心房黏液瘤。在更深的记忆中,患者报告了短暂的视力丧失。脑磁共振成像显示多发小胶质病变,提示系统性栓塞。患者通过右小开胸手术切除肿块。组织学分析证实了心房黏液瘤的诊断。该病例强调了STEMI中考虑栓塞病因的重要性,特别是在没有传统心血管危险因素的年轻患者中。
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
Giornale italiano di cardiologia
Giornale italiano di cardiologia CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
1.10
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:604180095
Book学术官方微信
小红书