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COVID-19 induced ventricular tachycardia storm unmasking a clinically silent cardiomyopathy: a case report
Saibal Mukhopadhyay1, Abhimanyu Uppal1, Jamal Yusuf1
1Department of Cardiology, GB Pant Institute of Post Graduate Education and Research, JLN Road, New Delhi 110002, India.
Insights
A COVID-19 cytokine surge triggered ventricular tachycardia storms and revealed silent Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) in a patient. This case highlights a severe COVID-19 presentation and links inflammation to arrhythmias.
Area of Science:
- Cardiology
- Infectious Diseases
- Genetics
Background:
- Coronavirus disease (COVID-19) can cause systemic inflammation, leading to cytokine storms that affect multiple organs.
- This systemic inflammation may trigger malignant ventricular arrhythmias and unmask underlying cardiomyopathies.
- Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) is a genetic heart muscle disease that can lead to life-threatening arrhythmias.
Observation:
- A 57-year-old male with hyperthyroidism and diabetes presented with recurrent ventricular tachycardia (VT).
- He was incidentally diagnosed with COVID-19, despite lacking typical respiratory symptoms.
- Elevated inflammatory markers and cardiac troponin T correlated with increased ventricular ectopy, resolving as COVID-19 cleared.
Findings:
- The patient was diagnosed with Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) through electrocardiogram and echocardiography.
- A severe COVID-19 cytokine surge was implicated in triggering VT storm and unmasking silent ARVC.
- This represents a novel and severe presentation of COVID-19, linking inflammation to arrhythmogenicity.
Implications:
- This case underscores the potential for COVID-19 to precipitate severe cardiac events, including VT storms.
- It suggests a direct link between COVID-19-induced inflammation and the development or unmasking of arrhythmogenic cardiomyopathies.
- Further research is warranted to explore the mechanisms connecting viral infections, inflammation, and cardiac arrhythmogenicity.
Background:
Coronavirus disease (COVID-19) is a systemic illness characterized by raging impact of cytokine storm on multiple organs. This may trigger malignant ventricular arrhythmias and unmask a clinically silent cardiomyopathy.
Case Summary:
A 57-year-old gentleman, known case of hyperthyroidism and diabetes, was referred to our emergency department with history of two ventricular tachycardia (VT) episodes requiring direct current cardioversion in last 3 h followed by another episode in our emergency department that was cardioverted. There was no past history of cardiac illness. His 12-lead electrocardiogram (during sinus rhythm) along with screening echocardiography suggested Arrhythmogenic right ventricular cardiomyopathy (ARVC). He was coincidentally found to be COVID-19 positive by reverse transcription-polymerase chain reaction (RT-PCR) as part of our routine screening. However, he had no fever or respiratory complaints. We noted raised systemic inflammatory markers and cardiac troponin T which progressively increased over the next 4 weeks paralleled by an increase in ventricular premature contraction burden and thereafter started decreasing and returned to baseline by 6th week when the patient became COVID-19 negative by RT-PCR. Subsequently, a single-chamber automated implantable cardioverter-defibrillator implantation was done following which there was a transient increase in these biomarkers that subsided spontaneously. The patient is asymptomatic during 6 weeks of follow-up.
Discussion:
COVID-19-associated cytokine surge triggering VT storm and unmasking a clinically silent ARVC has not yet been reported. The case highlights a life-threatening presentation of COVID-19 and indicates a probable link between inflammation and arrhythmogenicity.
Related Concept Videos
Cardiomyopathy I: Introduction and Classification
Dysrhythmias III: Characteristics of Dysrhythmias
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Myocarditis I: Introduction
Myocarditis II: Clinical Features and Diagnostic Tests

