Benjamin Wei-Liang Ng, Keng-Tat Koh, Martin Ngie-Liong Wong
{"title":"Idiopathic right ventricular outflow tract ventricular tachycardia-induced cardiomyopathy masquerading as MIS-C-associated myocarditis in a child.","authors":"Benjamin Wei-Liang Ng, Keng-Tat Koh, Martin Ngie-Liong Wong","doi":"10.1136/bcr-2025-267822","DOIUrl":null,"url":null,"abstract":"<p><p>A previously healthy early adolescent male presented with respiratory distress and lethargy during the COVID-19 pandemic. Evaluation revealed ventricular tachycardia (VT), hepatomegaly, pleural effusion and cardiomegaly with impaired cardiac function. Positive COVID-19 antibodies suggested Multisystem Inflammatory Syndrome in Children (MIS-C)-associated myocarditis. Treatment with intravenous immunoglobulin, anti-inflammatory agents and amiodarone led to normalised cardiac function and arrhythmia resolution. However, VT recurred with myocardial dysfunction after stopping amiodarone. Further ECG reassessment identified focal VT originating from the right ventricular outflow tract (RVOT). Cardiac magnetic resonance showed no myocardial scarring, supporting the diagnosis of idiopathic RVOT-VT. Radiofrequency ablation was performed successfully, and the patient remained VT-free at 1-year follow-up. This case describes the rare presentation of idiopathic RVOT-VT causing cardiomyopathy, initially mimicking myocarditis. It highlights the limitations of current diagnostic modalities in distinguishing VT-induced cardiomyopathy from myocarditis and emphasises careful ECG and imaging evaluation to guide appropriate management and improve outcomes.</p>","PeriodicalId":9080,"journal":{"name":"BMJ Case Reports","volume":"18 9","pages":""},"PeriodicalIF":0.6000,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMJ Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1136/bcr-2025-267822","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
A previously healthy early adolescent male presented with respiratory distress and lethargy during the COVID-19 pandemic. Evaluation revealed ventricular tachycardia (VT), hepatomegaly, pleural effusion and cardiomegaly with impaired cardiac function. Positive COVID-19 antibodies suggested Multisystem Inflammatory Syndrome in Children (MIS-C)-associated myocarditis. Treatment with intravenous immunoglobulin, anti-inflammatory agents and amiodarone led to normalised cardiac function and arrhythmia resolution. However, VT recurred with myocardial dysfunction after stopping amiodarone. Further ECG reassessment identified focal VT originating from the right ventricular outflow tract (RVOT). Cardiac magnetic resonance showed no myocardial scarring, supporting the diagnosis of idiopathic RVOT-VT. Radiofrequency ablation was performed successfully, and the patient remained VT-free at 1-year follow-up. This case describes the rare presentation of idiopathic RVOT-VT causing cardiomyopathy, initially mimicking myocarditis. It highlights the limitations of current diagnostic modalities in distinguishing VT-induced cardiomyopathy from myocarditis and emphasises careful ECG and imaging evaluation to guide appropriate management and improve outcomes.
期刊介绍:
BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.