Symptomatic arrhythmogenic right ventricular dysplasia/cardiomyopathy. A two-centre retrospective study of 15 symptomatic ARVD/C cases and focus on the diagnostic value of MRI in symptomatic ARVD/C patients

被引:9
作者
Dewillde, Willem [1 ]
Boersma, Lucas [1 ]
Delanote, Joost [3 ]
Pollet, Peter [2 ]
Scholzel, Bastiaan [1 ]
Wever, Eric [1 ]
Vandekerckhove, Yves [2 ]
机构
[1] AZ Sint Antonius Nieuwegein, Dept Cardiol, Nieuwegein, Netherlands
[2] AZ St Jan Brugge, Dept Cardiol, Brugge, Belgium
[3] AZ St Jan Brugge, Dept Radiol, Brugge, Belgium
关键词
arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C); ARVC; ICD; cardiomyopathy; sudden death; arrhythmia; tachycardia;
D O I
10.2143/AC.63.2.2029526
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background - Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is associated with sudden death in the young and heart failure in the elderly. The purpose is to review 15 symptomatic ARVD/C cases and also to describe the use of MRI as a diagnostic tool. Methods and results - This retrospective analysis includes 15 patients who presented with symptomatic ARVD/C. Diagnosis was made upon the criteria proposed by the European Society of Cardiology. In all patients there was at least 1 or more abnormal MRI sign. The most frequent abnormalities were focal right ventricular dyskinesia (64%), MRI fatty infiltration (57%) and right ventricular aneurysm or right ventricular outflow tract microaneurysms (57%). Presenting symptoms were palpitations (60%), atypical chest pain (46%), syncope (40%), and aborted sudden death (26%). T-inversion in V2-V3 was seen in 60% of the patients. Thirteen patients (86%) received an ICD implantation. The mean follow-up per patient was 89 months, which resulted in a total follow-up of 111 patient years. Forty-six percent of the patients with an ICD had one or more appropriate shocks during follow-up. To this date no mortality was reported. Conclusion - This retrospective study demonstrates that symptomatic ARVD/C patients typically present with symptoms of syncope, palpitations in association with ventricular tachycardia and in a quarter of the cases with aborted sudden cardiac death. The electrocardiogram mostly shows T inversion in the anterior leads. All patients were treated with medication and ICD-implantation or VT-ablation. The malignant nature of the disease in symptomatic ARVD/C patients is stressed by the fact that the presenting symptom is aborted sudden death in a quarter of the cases and the fact that nearly half of the patients with an ICD had at least one appropriate shock during follow-up. There was an abnormal MRI in 100% of the investigated patients. In 20% (3 patients), the MRI criterion (right ventricular dilatation/bulging/aneurysm) was necessary to meet the ESC criteria. Therefore it has become an important tool in our diagnostic work-up when ARVD/C is suspected. We also suggest a change in the diagnostic criteria of ARVD/C. Whereas fatty infiltration seen on RV biopsy is a major criterion, MRI fatty infiltration is not regarded as a diagnostic criterion by the task force to this day.
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收藏
页码:181 / 189
页数:9
相关论文
共 30 条
[1]   Histologic findings in patients with clinical and instrumental diagnosis of sporadic arrhythmogenic right ventricular dysplasia [J].
Chimenti, C ;
Pieroni, M ;
Maseri, A ;
Frustaci, A .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2004, 43 (12) :2305-2313
[2]   Implantable cardioverter-defibrillator therapy for prevention of sudden death in patients with Arrhythmogenic right ventricular cardiomyopathy/dysplasia [J].
Corrado, D ;
Leoni, L ;
Link, MS ;
Della Bella, P ;
Gaita, F ;
Curnis, A ;
Salerno, JU ;
Igidbashian, D ;
Raviele, A ;
Disertori, M ;
Zanotto, G ;
Verlato, R ;
Vergara, G ;
Delise, P ;
Turrini, P ;
Basso, C ;
Naccarella, F ;
Maddalena, F ;
Estes, NAM ;
Buja, G ;
Thiene, G .
CIRCULATION, 2003, 108 (25) :3084-3091
[3]   SUDDEN-DEATH IN YOUNG COMPETITIVE ATHLETES - CLINICOPATHOLOGICAL CORRELATIONS IN 22 CASES [J].
CORRADO, D ;
THIENE, G ;
NAVA, A ;
ROSSI, L ;
PENNELLI, N .
AMERICAN JOURNAL OF MEDICINE, 1990, 89 (05) :588-596
[4]   Sudden cardiac death in young people with apparently normal heart [J].
Corrado, D ;
Basso, C ;
Thiene, G .
CARDIOVASCULAR RESEARCH, 2001, 50 (02) :399-408
[5]  
Dewilde W, 2005, CIRCULATION, V112, pE68
[6]   Arrhythmogenic right ventricular cardiomyopathies - Clinical forms and main differential diagnoses [J].
Fontaine, G ;
Fontaliran, F ;
Frank, R .
CIRCULATION, 1998, 97 (16) :1532-1535
[7]   Histology of sudden death in arrhythmogenic right ventricular cardiomyopathy/dysplasia [J].
Fontaine, G ;
Fornes, P .
CIRCULATION, 2004, 110 (03) :E20-E20
[8]   Ventricular tachycardia catheter ablation in arrhythmogenic right ventricular dysplasia: A 16-year experience [J].
Fontaine G. ;
Tonet J. ;
Gallais Y. ;
Lascault G. ;
Hidden-Lucet F. ;
Aouate P. ;
Halimi F. ;
Poulain F. ;
Johnson N. ;
Charfeddine H. ;
Frank R. .
Current Cardiology Reports, 2000, 2 (6) :498-506
[9]  
Fontaine G, 1999, ACTA CARDIOL, V54, P189
[10]   Prospective evaluation of relatives for familial arrhythmogenic right ventricular cardiomyopathy/dysplasia reveals a need to broaden diagnostic criteria [J].
Hamid, MS ;
Norman, M ;
Quraishi, A ;
Firoozi, S ;
Thaman, R ;
Gimeno, JR ;
Sachdev, B ;
Rowland, E ;
Elliott, PM ;
McKenna, WJ .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2002, 40 (08) :1445-1450