Mittal Ashish, Navaratnarajah Manoraj, Harden Stephen, Velissaris Theodore, Roberts Paul R
Dept. of Cardiac Electrophysiology, St Bartholomew's Hospital Heart Centre, London EC1A 7BE, UK.
Dept. of Cardiothoracic Surgery, University Hospital Southampton, Southampton SO16 6YD, UK.
Eur Heart J Case Rep. 2024 Jun 14;8(7):ytae298. doi: 10.1093/ehjcr/ytae298. eCollection 2024 Jul.
Left atrial appendage aneurysm (LAAA) is a rare cardiac anomaly, which can be congenital or acquired in origin. Because most cases are asymptomatic, it is typically diagnosed incidentally in the second to third decades of life. We present a case of a 28-year-old male with refractory atrial tachyarrhythmias and significantly reduced exercise tolerance. The informed consent was given by patient for this manuscript.
We present a case of a 28-year-old male with refractory atrial tachyarrhythmias and significantly reduced exercise tolerance after an episode of COVID respiratory infection. He was referred by primary care physician for management of atrial fibrillation (AF) with CHA2DS2Vasc score zero. He had documented AF and atrial flutter (AFL) resistant to both chemical and electrical cardioversions. Initial portable focused transthoracic echocardiography documented borderline reduced left ventricular ejection fraction in context of AFL. Electrophysiological study confirmed the diagnosis of typical AFL. Successful radiofrequency ablation of cavo-tricuspid isthmus resulted in bidirectional isthmus conduction block. However, patient developed AF, which was electrically cardioverted at the end of procedure. Patient was discharged on bisoprolol, ramipril, and apixaban, and outpatient cardiac MRI was organized to look for post-COVID myocardial scarring. Patient had recurrence of symptoms, and this time it was due to AF. Multimodal imaging led to discovery of LAAA, in which after discussion in multidisciplinary meeting, he was accepted for and managed with surgical resection of LAAA with concomitant Cox-Maze IV procedure. On 9 months post-operative follow up, patient is maintaining sinus rhythm and has completely returned to baseline activities.
A young patient with refractory atrial arrhythmia should be referred for multimodal cardiovascular imaging to rule out any structural heart disease. Left atrial appendage aneurysm is rare and can be managed conservatively, but surgical excision is most reported and appears to favour arrhythmia-free survival.
左心耳动脉瘤(LAAA)是一种罕见的心脏异常,其起源可以是先天性的或后天获得的。由于大多数病例无症状,通常在生命的第二个十年到第三个十年偶然被诊断出来。我们报告一例28岁男性,患有难治性房性快速性心律失常且运动耐量显著降低。患者已对本稿件给予知情同意。
我们报告一例28岁男性,在新冠呼吸道感染发作后出现难治性房性快速性心律失常且运动耐量显著降低。他被初级保健医生转诊来管理CHA2DS2Vasc评分为零的房颤(AF)。他有记录显示AF和房扑(AFL)对药物和电复律均耐药。最初的便携式经胸超声心动图记录显示在AFL情况下左心室射血分数临界降低。电生理研究证实了典型AFL的诊断。成功的腔静脉 - 三尖瓣峡部射频消融导致双向峡部传导阻滞。然而,患者随后发生AF,在手术结束时进行了电复律。患者出院时服用比索洛尔、雷米普利和阿哌沙班,并安排了门诊心脏磁共振成像以寻找新冠后心肌瘢痕。患者症状复发,此次是由于AF。多模态成像发现了LAAA,在多学科会议讨论后,他接受了LAAA手术切除并同时进行Cox - Maze IV手术。术后9个月随访时,患者维持窦性心律,已完全恢复到基线活动水平。
对于患有难治性房性心律失常的年轻患者,应转诊进行多模态心血管成像以排除任何结构性心脏病。左心耳动脉瘤罕见,可保守治疗,但手术切除报道最多,似乎有利于无心律失常生存。