掩盖心脏肉瘤病的房室结再发性心动过速:一份临床病例报告。

Pub Date : 2024-09-27 eCollection Date: 2024-10-01 DOI:10.1093/ehjcr/ytae539
Laura Casteur, Thomas Rosseel, Margaretha Van Kerrebroeck, Lucas Van Aelst, Joris Ector
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引用次数: 0

摘要

背景:肉样瘤病是一种罕见疾病,心脏受累的患者只占少数。临床症状取决于非溃疡性肉芽肿在心脏中的位置,从无症状到房室传导阻滞、室性心律失常、心力衰竭和心脏性猝死不等。临床表现为室上性心动过速的心脏肉样瘤病很少见。病例摘要:我们介绍了一例女性患者的病例,她出现房室结再入性心动过速是心脏肉样瘤病不常见的首发症状。她的静息心电图显示完全性左束支传导阻滞和一级房室传导阻滞。住院期间,她不断在窦性心律伴有一级房室传导阻滞、2:1房室传导阻滞和房室结再入性心动过速之间转换:重要的是要知道,心脏肉样瘤病很少以室上性心动过速为首发症状。鉴于心脏性猝死的风险升高,早期发现至关重要,所有需要永久起搏的患者都应考虑植入心律转复除颤器。
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Atrioventricular nodal re-entrant tachycardia unmasking cardiac sarcoidosis: a clinical case report.

Background: Sarcoidosis is a rare disease, and cardiac involvement is seen in the minority of patients. The clinical symptoms depend on the location of the noncaseating granulomas in the heart and vary from asymptomatic to atrioventricular (AV) conduction block, ventricular arrhythmia, heart failure, and sudden cardiac death. Clinically manifest cardiac sarcoidosis seldomly presents with supraventricular tachycardia.

Case summary: We present a case where a female patient presented with AV nodal re-entrant tachycardia as an uncommon initial presentation of cardiac sarcoidosis. Her resting electrocardiogram showed a complete left bundle branch block and first-degree AV conduction block. During hospitalization, there was continuous switching between sinus rhythm with first-degree AV block, 2:1 AV block, and AV nodal re-entrant tachycardia.

Discussion: It is important to be aware that cardiac sarcoidosis can rarely present with supraventricular tachycardia as initial symptom. Given the elevated risk of sudden cardiac death, early detection is crucial and all patients who require permanent pacing should be considered for implantable cardioverter-defibrillator implantation.

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