源于右心房游离壁憩室的房性心动过速:病例报告。

Pub Date : 2024-09-12 eCollection Date: 2024-10-01 DOI:10.1093/ehjcr/ytae497
Shuang Zhang, Yichao Xiao, Die Hu, Mingxian Chen, Xuping Li
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引用次数: 0

摘要

背景:心房性心动过速(AT)是一种起源于心房的心律失常疾病,与房室结无关,包括基于不同机制的各种类型,如异常自动性、触发活动和再进入。这些机制通常与特定的解剖结构有关。病灶性 AT 虽然相对罕见,但通常产生于左右心房的著名位置,如肺静脉、二尖瓣环、终末嵴和冠状动脉窦腔。病例摘要:我们报告了一例源自右心房游离壁憩室的罕见 AT 病例。患者的心动过速反复发作,对标准治疗无效。详细的电生理图确定了心动过速的不寻常起源是右心房游离壁憩室。成功实施导管消融术后,心律失常得以缓解,随访期间患者仍无症状:本病例拓展了人们对心动过速起源的认识,强调了右心房游离壁憩室是心动过速的一个潜在来源,尽管这种来源非常罕见。该病例强调了综合电生理图谱的重要性,尤其是在非典型的 AT 表现中。该病例的成功消融强调了即使在不常见的解剖部位也可以进行有针对性的干预。我们还需要进一步研究,以评估此类罕见部位心动过速的发病率和临床意义。
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Atrial tachycardia originating from a right atrial free wall diverticulum: case report.

Background: Atrial tachycardia (AT) is an arrhythmic disorder originating from the atrium, independent of the atrioventricular node, and includes various types based on different mechanisms such as abnormal automaticity, triggered activity, and re-entry. These mechanisms are often related to specific anatomical structures. Focal AT, though relatively rare, typically arises from well-known locations in the left and right atria, such as the pulmonary veins, mitral valve annulus, crista terminalis, and coronary sinus ostium.

Case summary: We report a rare case of AT originating from a diverticulum in the right atrial free wall. The patient experienced recurrent AT episodes resistant to standard treatments. Detailed electrophysiological mapping identified the unusual origin of the tachycardia from a right atrial free wall diverticulum. Catheter ablation was successfully performed, leading to the resolution of the arrhythmia, with the patient remaining symptom-free during follow-up.

Discussion: This case expands the understanding of AT origins, highlighting the right atrial free wall diverticulum as a potential, though rare, source of tachycardia. The case emphasizes the importance of comprehensive electrophysiological mapping, especially in atypical presentations of AT. Successful ablation in this instance underscores the potential for targeted interventions even in uncommon anatomical sites. Further studies are needed to assess the prevalence and clinical significance of AT arising from such rare locations.

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