Abstract
Differentiating arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) from other cardiomyopathies is clinically important but challenging. Although the modified Task Force Criteria can facilitate diagnosis of ARVD/C according to clinical manifestations, histopathological examination plays a pivotal role in excluding other diseases that can mimic ARVD/C. Here, we report a patient with amyloidosis that initially presented similarly to ARVD/C. The diagnosis was confirmed by endomyocardial biopsy, and catheter ablation eliminated the ventricular tachyarrhythmias through an epicardial approach.
Original language | English |
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Pages (from-to) | 282-285 |
Number of pages | 4 |
Journal | Korean Circulation Journal |
Volume | 47 |
Issue number | 2 |
DOIs | |
State | Published - Mar 2017 |
Keywords
- Amyloidosis
- Arrhythmogenic right ventricular cardiomyopathy-dysplasia
- Biopsy
- Catheter ablation
- Ventricular tachycardia