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Catheter Ablation of Ventricular Tachycardia/Fibrillation in a Patient with Right Ventricular Amyloidosis with Initial Manifestations Mimicking Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
Korean Circulation Journal ; : 282-285, 2017.
Article in English | WPRIM (Western Pacific) | ID: wpr-59177
Responsible library: WPRO
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.
Subject(s)

Full text: Available Health context: SDG3 - Target 3.4 Reduce premature mortality due to noncommunicable diseases Health problem: Cardiovascular Disease / Congenital and Chromosomal Anomalies / Endocrine System Diseases / Other circulatory Diseases Database: WPRIM (Western Pacific) Main subject: Tachycardia / Biopsy / Tachycardia, Ventricular / Catheter Ablation / Arrhythmogenic Right Ventricular Dysplasia / Advisory Committees / Diagnosis / Catheters / Amyloidosis / Cardiomyopathies Type of study: Diagnostic study Limits: Humans Language: English Journal: Korean Circulation Journal Year: 2017 Document type: Article
Full text: Available Health context: SDG3 - Target 3.4 Reduce premature mortality due to noncommunicable diseases Health problem: Cardiovascular Disease / Congenital and Chromosomal Anomalies / Endocrine System Diseases / Other circulatory Diseases Database: WPRIM (Western Pacific) Main subject: Tachycardia / Biopsy / Tachycardia, Ventricular / Catheter Ablation / Arrhythmogenic Right Ventricular Dysplasia / Advisory Committees / Diagnosis / Catheters / Amyloidosis / Cardiomyopathies Type of study: Diagnostic study Limits: Humans Language: English Journal: Korean Circulation Journal Year: 2017 Document type: Article
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