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持续性室性心动过速是心脏淀粉样变性的先兆。

Sustained Ventricular Tachycardia as a Harbinger of Cardiac Amyloidosis.

机构信息

Cardiovascular Division, Department of Medicine, Tower Health Medical Group, Reading Hospital, West Reading, PA, USA.

Division of Medical Critical Care, Boston Children's Hospital, Boston, MA, USA.

出版信息

Am J Case Rep. 2020 Dec 7;21:e927041. doi: 10.12659/AJCR.927041.

Abstract

BACKGROUND Cardiac amyloidosis is an infiltrative cardiomyopathy caused by the extracellular deposition of insoluble precursor protein amyloid fibrils. These depositions of protein amyloid fibrils are found on the atria and ventricles and can cause a wide array of arrhythmias; however, sustained ventricular arrhythmias are quite uncommon. CASE REPORT A 71-year-old man with a history of hypertension developed a sudden onset of shortness of breath, profuse diaphoresis, lightheadedness, and presyncope. Upon emergency medical services' arrival, an initial electrocardiogram revealed wide complex tachycardia with a heart rate of 220 to 230 beats per min. He was subsequently given, in succession, magnesium, adenosine, and amiodarone with no change in heart rate or rhythm. Due to ongoing symptoms of diaphoresis and the development of dyspnea, he underwent direct current cardioversion and was converted from ventricular tachycardia to atrial fibrillation at controlled rates. A transthoracic echocardiogram and cardiac magnetic resonance imaging showed features suspicious for cardiac amyloidosis. A subsequent 99m technetium pyrophosphate single-photon emission computerized tomography scan revealed a grade 3 visual uptake and a heart-to-contralateral lung ratio of 1.92, consistent with transthyretin amyloidosis. The patient was treated with tafamidis and an implantable cardioverter-defibrillator for secondary prevention of ventricular arrhythmia. CONCLUSIONS This case highlights the need to consider cardiac amyloidosis in the differential diagnoses of patients with persistent ventricular arrhythmia and no prior history of heart disease.

摘要

背景

心脏淀粉样变性是一种浸润性心肌病,由不溶性前体蛋白淀粉样纤维的细胞外沉积引起。这些蛋白质淀粉样纤维的沉积物位于心房和心室,可引起广泛的心律失常;然而,持续性室性心律失常相当少见。

病例报告

一名 71 岁男性,有高血压病史,突然出现呼吸急促、大量出汗、头晕和晕厥。在紧急医疗服务到达时,初始心电图显示宽复合性心动过速,心率为 220 至 230 次/分。随后,他依次接受了镁、腺苷和胺碘酮治疗,但心率和节律均无变化。由于持续出汗和呼吸困难的症状,他接受了直流电复律,并在控制的速率下从室性心动过速转为心房颤动。经胸超声心动图和心脏磁共振成像显示出疑似心脏淀粉样变性的特征。随后的 99m 锝焦磷酸盐单光子发射计算机断层扫描显示 3 级视觉摄取和心脏与对侧肺的比值为 1.92,符合转甲状腺素淀粉样变性。该患者接受了塔法米迪治疗和植入式心脏复律除颤器,以预防室性心律失常的二次发作。

结论

本病例强调了在持续性室性心律失常且无先前心脏病史的患者鉴别诊断中需要考虑心脏淀粉样变性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9daf/7733151/0dcd2ffea5fe/amjcaserep-21-e927041-g001.jpg

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