第一例疑似病毒性心肌炎的左心房附件动脉瘤内镜切除:一种多模式入路-未经纠正的证明。

IF 0.6
Raheleh Kaviani, Seyed Shahin Eftekhari, Hamidreza Pouraliakbar, Saeid Hosseini, Hossein Nokhbezaeim, Haniyeh Faraji Azad, Ermia Tabandeh, Seyyed Mojtaba Hashemizadeh, Zahra Emkanjoo
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引用次数: 0

摘要

左心房附件动脉瘤(LAAA)是一种罕见的心血管异常,文献记载的病例不到200例。它通常伴有严重的并发症,如心律失常和血栓栓塞事件。最近的证据表明,病毒感染,特别是病毒性心肌炎,可能是LAAA的潜在原因。我们报告的情况下,36岁的妇女与哮喘史谁提出心悸和心房性心动过速两个月后,严重的上呼吸道感染。经胸超声心动图显示一个巨大的动脉瘤性左心房附件(LAA),尺寸为5.6 × 3.5 cm,左心室射血分数降低50%。心脏计算机断层扫描证实LAAA并显示异常血流动力学。晚期钆增强显示左心室壁后外侧段心外膜下中部高强化,与既往心肌炎一致。在经食管超声心动图的指导下,患者接受了一种新型的微创内镜胸腔镜动脉瘤切除术。未见血栓。手术在体外循环的辅助下顺利完成。本病例强调了病毒性心肌炎与LAAA之间的潜在联系,同时也承认了先天性和偶然发现的动脉瘤的可能性。它强调了多模态成像在准确诊断和管理中的关键作用。成功的微创手术切除和随后的心功能恢复证明了该方法的有效性,为LAAA患者提供了广阔的前景。临床医生应将病毒感染视为LAAA发展的潜在因素,并提倡早期诊断和干预以改善临床结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
First Case of Endoscopic Resection for Left Atrial Appendage Aneurysm with Suspected Viral Myocarditis: A Multimodal Approach-Uncorrected Proof.

Left atrial appendage aneurysm (LAAA) is a rare cardiovascular anomaly, with fewer than 200 documented cases. It is often associated with severe complications, such as arrhythmias and thromboembolic events. Recent evidence suggests that viral infections, particularly viral myocarditis, might be an underlying cause of LAAA. We report the case of a 36-year-old woman with a history of asthma who presented with palpitations and atrial tachyarrhythmia two months after a severe upper respiratory infection. Transthoracic echocardiography revealed a large aneurysmal left atrial appendage (LAA) measuring 5.6 × 3.5 cm and a reduced left ventricular ejection fraction of 50%. Cardiac computed tomography confirmed the LAAA and revealed abnormal flow dynamics. Late gadolinium enhancement showed mid-subepicardial hyperenhancement in the posterolateral segments of the left ventricular wall, consistent with a previous myocarditis. The patient underwent a novel, minimally invasive endoscopic thoracoscopic resection of the aneurysm, guided by transesophageal echocardiography. No thrombus was present. The procedure was successfully completed with the aid of cardiopulmonary bypass. This case highlights a potential association between viral myocarditis and LAAA, while also acknowledging the possibility of a congenital and incidentally discovered aneurysm. It underscores the critical role of multimodal imaging in accurate diagnosis and management. The successful minimally invasive surgical resection and subsequent restoration of cardiac function demonstrate the effectiveness of this approach, offering a promising outlook for patients with LAAA. Clinicians should consider viral infections as potential contributors to LAAA development and advocate for early diagnosis and intervention to improve clinical outcomes.

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