Clinically suspected acute right ventricular fulminant dengue myocarditis masquerading with dual lethal arrhythmias: a case report.

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL
Miftah Pramudyo, Iwan C S Putra, Mohammad Iqbal, Hawani S Prameswari, Giky Karwiky, Triwedya I Dewi, Pradana Raharjo, William Kamarullah, Norman Sukmadi
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Abstract

Background: Acute right ventricular myocarditis is rare, comprising only 18% of myocarditis cases. Despite being relatively infrequent at 12.4%, dengue-induced myocarditis has a high mortality risk of 26.4%. This report presents a novel case of acute fulminant right ventricular myocarditis due to severe dengue infection, complicated by dual electrical disturbances: complete heart block and ventricular tachycardia.

Case report: A 49-year-old Asian male patient was referred to our hospital with a temporary pacemaker due to a complete heart block. He had a history of recurrent syncope over three days and a fever five days before admission. Initial electrocardiography showed a total atrioventricular nodal block progressing to a high-degree atrioventricular block with a left bundle branch block, indicating an infra-Hisian block. Laboratory findings included thrombocytopenia, elevated troponin, high creatinine, increased liver transaminases, and a positive dengue nonstructural protein 1 test, confirming a diagnosis of dengue infection. Echocardiography showed reduced right ventricular systolic function, normal left ventricular systolic function (ejection fraction: 50%), and dyskinetic intraventricular septum. Coronary angiography revealed normal coronary anatomy. An endomyocardial biopsy was deferred due to severe thrombocytopenia. On the third day, the patient's condition worsened, developing cardiogenic shock and left ventricular systolic dysfunction (ejection fraction: 35%). He subsequently experienced a seizure and slow ventricular tachycardia originating from the right coronary cusp, followed by cardiac arrest. The patient's family claimed not to resuscitate the patient. Furthermore, the patient died shortly after.

Conclusion: This case underscores the critical need for prompt diagnosis and aggressive management of clinically suspected acute fulminant right ventricular myocarditis because complications can rapidly progress to left ventricular systolic dysfunction, leading to cardiogenic shock and sudden cardiac death.

临床疑似急性右心室暴发性登革热心肌炎合并双重致死性心律失常:病例报告。
背景:急性右心室心肌炎非常罕见,仅占心肌炎病例的 18%。尽管登革热诱发的心肌炎发病率相对较低,仅为 12.4%,但其死亡率却高达 26.4%。本报告介绍了一例严重登革热感染导致的急性暴发性右心室心肌炎的新病例,该病例并发双重心电紊乱:完全性心脏传导阻滞和室性心动过速:一名 49 岁的亚裔男性患者因完全性心脏传导阻滞而被转诊至我院,并安装了临时起搏器。入院前五天,他有三天反复晕厥和发烧的病史。最初的心电图显示完全性房室结传导阻滞发展为高位房室传导阻滞,伴有左束支传导阻滞,显示为 "希氏下传导阻滞"。实验室检查结果包括血小板减少、肌钙蛋白升高、肌酐升高、肝脏转氨酶升高,登革热非结构蛋白1检测呈阳性,确诊为登革热感染。超声心动图显示右室收缩功能减弱,左室收缩功能正常(射血分数:50%),室间隔运动障碍。冠状动脉造影显示冠状动脉解剖正常。由于血小板严重减少,心内膜活检被推迟。第三天,患者病情恶化,出现心源性休克和左心室收缩功能障碍(射血分数:35%)。随后,他出现癫痫发作和源自右冠状动脉尖的缓慢室性心动过速,随后心跳骤停。患者家属声称没有对患者进行抢救。此外,患者不久后死亡:本病例强调了对临床疑似急性暴发性右心室心肌炎进行及时诊断和积极治疗的重要性,因为并发症可迅速发展为左心室收缩功能障碍,导致心源性休克和心脏性猝死。
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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来源期刊
Journal of Medical Case Reports
Journal of Medical Case Reports Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
436
期刊介绍: JMCR is an open access, peer-reviewed online journal that will consider any original case report that expands the field of general medical knowledge. Reports should show one of the following: 1. Unreported or unusual side effects or adverse interactions involving medications 2. Unexpected or unusual presentations of a disease 3. New associations or variations in disease processes 4. Presentations, diagnoses and/or management of new and emerging diseases 5. An unexpected association between diseases or symptoms 6. An unexpected event in the course of observing or treating a patient 7. Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
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