Successful catheter ablation in an octogenarian with persistent atrial fibrillation complicated by cor triatriatum sinister: a case report.

Pub Date : 2024-09-10 eCollection Date: 2024-09-01 DOI:10.1093/ehjcr/ytae490
Yusuke Okuyama, Atsushi Tamura, Kohei Ueda, Shunzo Matsuoka, Yoshihisa Nakagawa
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Abstract

Background: Cor triatriatum sinister (CTS) is a rare congenital heart defect sometimes complicated with atrial fibrillation (AF). Catheter ablation (CA) relieves the AF-associated symptoms, but CA for AF with CTS has been reported rarely. Because CTS can be associated with other congenital heart disease, detailed preoperative assessment is important.

Case summary: An 80-year-old man was referred to our institution for shortness of breath that had persisted for 2 months when he was first diagnosed with AF. Transthoracic echocardiography revealed an enlarged left atrium (LA) divided into two chambers by a membrane. Transoesophageal echocardiography showed the membrane extending from the fossa ovalis (FO) to the Coumadin ridge, with the accessory (dorsal) chamber (AC) in closer proximity to the FO. Computed tomography showed that all pulmonary veins (PVs) flowed into the AC, with no PV anomalies. No other heart anomaly was identified, with no thrombus in the LA. With these findings, PV isolation (PVI) with CA was considered safe. Transseptal puncture was performed with intracardiac echocardiography for precise catheterization of the AC. Pulmonary vein isolation was performed successfully. The patient was discharged 4 days after the procedure, without any complications. His symptoms improved post-procedure, and sinus rhythm was maintained without antiarrhythmic drug therapy during the 18-month follow-up.

Discussion: Cor triatriatum sinister is a rare anomaly that accounts for 0.1% of all congenital heart diseases. Cor triatriatum sinister sometimes complicated with symptomatic AF. Detailed preoperative anatomical assessment with multiple imaging modalities helped us achieve safe and effective CA for a patient with AF and CTS, even in an octogenarian.

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一位八旬老人因持续性心房颤动并发窦性心房颤而成功接受导管消融术:病例报告。
背景:Cor triatriatum sinister(CTS)是一种罕见的先天性心脏缺陷,有时会并发心房颤动(AF)。导管消融术(CA)可缓解房颤相关症状,但对伴有 CTS 的房颤进行导管消融术的报道很少。病例摘要:一名 80 岁的男性因持续 2 个月的呼吸急促被转诊至我院,首次诊断为房颤。经胸超声心动图显示左心房(LA)增大,被一层膜分为两个心腔。经食道超声心动图显示,这层膜从卵圆窝(FO)延伸至 Coumadin 脊,附属(背侧)心腔(AC)更靠近卵圆窝。计算机断层扫描显示,所有肺静脉(PV)都流入 AC,没有肺静脉异常。没有发现其他心脏异常,LA也没有血栓。鉴于这些检查结果,使用CA进行肺静脉隔离(PVI)被认为是安全的。在进行心内超声心动图检查时进行了经脐穿刺,以精确导管插入 AC。肺静脉隔离手术顺利完成。患者在术后 4 天出院,未出现任何并发症。术后他的症状有所改善,在18个月的随访中,窦性心律得以维持,无需抗心律失常药物治疗:讨论:窦性心三尖瓣狭窄是一种罕见的异常,占所有先天性心脏病的0.1%。窦性三尖瓣狭窄有时会并发无症状房颤。术前通过多种影像学方式进行详细的解剖评估,帮助我们为一名房颤合并CTS的患者(即使是八旬老人)实施了安全有效的CA手术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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