Prospective Study of Cardiac Sarcoid Mimicking Arrhythmogenic Right Ventricular Dysplasia

Introduction: Case studies indicate that cardiac sarcoid may mimic the clinical presentation of arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C); however, the incidence and clinical predictors to diagnose cardiac sarcoid in patients who meet International Task Force criteria for AR...

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Veröffentlicht in:Journal of cardiovascular electrophysiology 2009-05, Vol.20 (5), p.473-476
Hauptverfasser: VASAIWALA, SMIT C., FINN, CYNTHIA, DELPRIORE, JEANNE, LEYA, FRED, GAGERMEIER, JAMES, AKAR, JOSEPH G., SANTUCCI, PETER, DAJANI, KHALED, BOVA, DAVIDE, PICKEN, MARIA M., BASSO, CRISTINA, MARCUS, FRANK, WILBER, DAVID J.
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Sprache:eng
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Zusammenfassung:Introduction: Case studies indicate that cardiac sarcoid may mimic the clinical presentation of arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C); however, the incidence and clinical predictors to diagnose cardiac sarcoid in patients who meet International Task Force criteria for ARVD/C are unknown. Methods and Results: Patients referred for evaluation of left bundle branch block (LBBB)‐type ventricular arrhythmia and suspected ARVD/C were prospectively evaluated by a standardized protocol including right ventricle (RV) cineangiography‐guided myocardial biopsy. Sixteen patients had definite ARVD/C and four had probable ARVD/C. Three patients were found to have noncaseating granulomas on biopsy consistent with sarcoid. Age, systemic symptoms, findings on chest X‐ray or magnetic resonance imaging (MRI), type of ventricular arrhythmia, RV function, ECG abnormalities, and the presence or duration of late potentials did not discriminate between sarcoid and ARVD/C. Left ventricular dysfunction (ejection fraction
ISSN:1045-3873
1540-8167
DOI:10.1111/j.1540-8167.2008.01351.x