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Cardiac sarcoidosis is a potentially life-threatening manifestation of systemic sarcoidosis characterized by non-caseating granulomatous inflammation of the myocardium, conduction system, or other cardiac structures.
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It is underdiagnosed and can lead to arrhythmias, heart block, heart failure, and sudden cardiac death.
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Clinical Features of Cardiac Sarcoidosis (Top left) Small patches of basal involvement, usually clinically silent disease. (Top right) Large area of septal involvement often clinically manifests as heart block. (Bottom left) Re-entrant circuit involving an area of fibrosis/granuloma leading to ventricular tachycardia. (Bottom right) Extensive areas of LV and RV involvement often clinically manifest as heart failure ± heart block ± VT.
LV = left ventricular; RV = right ventricular; VT = ventricular tachycardia.
Birnie DH, Nery PB, Ha AC, Beanlands RSB. Cardiac Sarcoidosis. Journal of the American College of Cardiology. 2016;68(4):411-421. doi:https://doi.org/10.1016/j.jacc.2016.03.605
| Feature | Details |
|---|---|
| Conduction abnormalities | AV block (esp. complete heart block), bundle branch block |
| Arrhythmias | Ventricular tachycardia (VT), premature ventricular contractions |
| Heart failure | Dilated cardiomyopathy; may mimic idiopathic DCM |
| Chest pain / angina | Granulomatous involvement mimicking ischemia |
| Sudden cardiac death | Often due to ventricular arrhythmias or complete heart block |
Electrocardiographic Findings
| Finding | Significance |
|---|---|
| AV block (1st to 3rd degree) | Most common ECG abnormality |
| RBBB, LBBB | Common conduction defects |
| Ventricular arrhythmias | NSVT, sustained VT, PVCs |
| Prolonged QT, ST changes | Non-specific; may mimic ischemia |