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特发性左心室室性心动过速和纵隔淋巴结病与保存心室功能患者的肉芽肿浸润有关。

Monomorphic ventricular tachycardia and mediastinal adenopathy due to granulomatous infiltration in patients with preserved ventricular function.

机构信息

Cardiac Arrhythmia Services, CARE Hospital, Road Number 1, Banjara Hills, Hyderabad, Andhra Pradesh, India.

出版信息

J Am Coll Cardiol. 2011 Jun 28;58(1):48-55. doi: 10.1016/j.jacc.2011.02.044.

Abstract

OBJECTIVES

This report characterizes a syndrome of granulomatous infiltration presenting as sustained monomorphic ventricular tachycardia (SMVT) with mediastinal adenopathy in patients with preserved ventricular function.

BACKGROUND

Unlike truly idiopathic ventricular tachycardia, SMVT due to granulomatous infiltration responds poorly to radiofrequency ablation and has a poor prognosis.

METHODS

Patients without obstructive coronary artery disease and with normal ventricular function presenting with SMVT other than posterior fascicular morphology were evaluated. Computed chest tomograms, cardiac magnetic resonance imaging, and 18-fluorodeoxyglucose positron emission tomographic scans ((18)FDG PET-CT) were performed. Significant lymph nodes were evaluated for tuberculosis and sarcoidosis. Initial treatment included antiarrhythmic drugs ± radiofrequency ablation. Additionally, patients with evidence of tuberculosis received anti-tuberculosis therapy; the rest were treated as sarcoidosis.

RESULTS

Mediastinal adenopathy with mid-myocardial scar and/or focal myocardial inflammation was observed in 14 patients; lymph nodes revealed noncaseating granulomas in all. Evidence of tuberculosis was present in 79%. During follow-up (median duration 25 months), SMVT recurred despite initial treatment in 92%. Addition of disease-specific therapy abolished further recurrences in 64% of them. Decrease in SMVT correlated with resolution of myocardial inflammation on serial (18)FDG PET-CTs. Appropriate therapies occurred in 67% of patients receiving implantable cardioverter-defibrillators.

CONCLUSIONS

A subset of patients with SMVT with preserved ventricular function has a syndrome of arrhythmogenic myocarditis with granulomatous mediastinal adenopathy due to myocardial tuberculosis or cardiac sarcoidosis. This entity is optimally managed with a combination of disease-specific therapy and antiarrhythmic measures.

摘要

目的

本报告描述了一种肉芽肿浸润综合征,其特征为伴有纵隔淋巴结病的持续性单形性室性心动过速(SMVT),且患者心室功能正常。

背景

与真正的特发性室性心动过速不同,由肉芽肿浸润引起的 SMVT 对射频消融反应不佳,预后较差。

方法

评估了无阻塞性冠状动脉疾病且心室功能正常、表现为非后间隔形态的 SMVT 的患者。进行了胸部计算机断层扫描、心脏磁共振成像和 18-氟脱氧葡萄糖正电子发射断层扫描(18FDG PET-CT)。对有结核和结节病表现的显著淋巴结进行评估。初始治疗包括抗心律失常药物±射频消融。此外,有结核病证据的患者接受抗结核治疗;其余患者按结节病治疗。

结果

14 例患者均有纵隔淋巴结病伴中心肌瘢痕和/或局灶性心肌炎症;所有患者的淋巴结均显示非干酪样肉芽肿。有结核病证据的患者占 79%。在随访期间(中位时间 25 个月),尽管初始治疗,但 92%的患者 SMVT 仍复发。在其中 64%的患者中,添加特定疾病的治疗可消除进一步的复发。SMVT 的减少与连续 18FDG PET-CT 上心肌炎症的消退相关。在接受植入式心脏复律除颤器的患者中,有 67%的患者接受了适当的治疗。

结论

一部分伴有心室功能正常的 SMVT 患者存在由心肌结核或心脏结节病引起的致心律失常性心肌炎伴纵隔淋巴结病综合征。该病症通过特定疾病的治疗和抗心律失常措施的联合治疗效果最佳。

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