Comment j'explore⋯ Une suspicion de dysplasie arythmogéne du ventricule droit

[fr] La dysplasie arythmogène du ventricule droit est une pathologie rare, mais non exceptionnelle, associant la survenue d’arythmies pouvant être mortelles à une détérioration progressive de la structure et de la fonction du ventricule droit. Dans cet article, nous rappelons les bases étiopathogéniques de l’affection et insistons sur la démarche diagnostique.

Disciplines :

Cardiovascular & respiratory systems

Author, co-author :

BENOIT, Arnaud ; Centre Hospitalier Universitaire de Liège - CHU > Service de cardiologie

DAVIN, Laurent ; Centre Hospitalier Universitaire de Liège - CHU > Cardiologie

GACH, Olivier ; Centre Hospitalier Universitaire de Liège - CHU > Cardiologie

CAMUS, B

D'ORIO, Virginie ; Centre Hospitalier Universitaire de Liège - CHU > Cardiologie

PIERARD, Luc ; Centre Hospitalier Universitaire de Liège - CHU > Cardiologie

Language :

French

Title :

Comment j'explore⋯ Une suspicion de dysplasie arythmogéne du ventricule droit

Alternative titles :

[en] How I explore a case of suspected arhrhythmogenic right ventricularr dysplasiia

Publication date :

2014

Journal title :

Revue Médicale de Liège

ISSN :

0370-629X

eISSN :

2566-1566

Publisher :

Université de Liège. Revue Médicale de Liège, Liège, Belgium

Peer reviewed :

Peer reviewed

Available on ORBi :

since 01 March 2018

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Bibliography

Sen-Chowdhry S, Lowe MD, Sporton SC, et al. - Arrhythmogenic right ventricular cardiomyopathy: clinical presentation, diagnosis, and management. Am J Med, 2004, 117, 685-695.
Gemayel C, Pelliccia A, Thompson PD. - Arrhythmogenic right ventricular cardiomyopathy. J Am Coll Cardiol, 2001, 38, 1773-1781.
B. Murray. - Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C): a review of molecular and clinical literature. J Genet Counsel, 2012, 21, 494-504.
Kaplan SR, Gard JJ, Protonotarios N, et al. - Remodeling of myocyte gap junctions in arrhythmogenic right ventricular cardiomyopathy due to a deletion in plakoglobin (Naxos disease). Heart Rhythm, 2004, 1, 3-11.
Saffitz JE, Asimaki A, Huang H. - Arrhythmogenic right ventricular cardiomyopathy: new insights into mechanisms of disease. Cardio Pathol, 2010, 19, 166-170.
Sen-Chowdhry S, Syrris P, Pantazis A, et al. - Mutational heterogeneity, modifier genes, and environmental influences contribute to phenotypic diversity of arrhythmogenic cardiomyopathy. Circ Cardiovasc Genet, 2010, 3, 323-330.
Burke A P, Farb A, Tashko G, et al. - Arythmogenic right ventricular cardiomyopathy and fatty replacement of the right ventricular myocardium: are they different diseases? Circulation, 1998, 97, 1571-1580.
Corrado D, Basso C, Thiene G, et al. - Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasiaa multicenter study. J Am Coll Cardiol, 1997, 30, 1512-1520.
Marcus FI, McKenna WJ, Sherrill D, et al. - Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force criteria. Circulation, 2010, 121, 1533-1541.
Hauer HN, Cox MG, Groeneweg JA. - Impact of new electrocardiographic criterian arrhythmogenic cardiomyopathy. Frontiers in physiology, 2012, 3, 352.
Marcus FI, Zareba W. - The electrocardiogram in right ventricular cardiomyopathy/dysplasia. How can the electrocardiogram assist in understanding the pathologic and functional changes of the heart in this disease? J Electrocardiol, 2009, 42, 135-136.
Yoerger DM, Marcus F, Sherrill D, et al. - Echocardiographic findings in patients meeting Task Force Criteria for arrhythmogenic right ventricular dysplasia new insights from the multidisciplinary study of right ventricular dysplasia. J Am Coll Cardiol, 2005, 45, 860-865.
Murphy DT, Shine SC, Cradock A, et al. - Cardiac MRI in arrhythmogenic right ventricular cardiomyopathy. Am J Roentgenol, 2010, 194, 299-306.
Ahmed J, Smith WM, Ruygrok PN, et al. - Right ventricular morphology on catheter angiography: Variations and its implications for the diagnosis of arrhythmogenic right ventricular cardiomyopathy. Heart Lung Cir, 2012, 21, 700-705.
Wichter T, Schäfers M, Rhodes CG, et al. - Cardiomyopathy: quantitative assessment of presynaptic norepinephrine reuptake and abnormalities of cardiac sympathetic innervation in arrhythmogenic right ventricular postsynaptic b-Adrenergic receptor density with positron emission tomography. Circulation, 2000, 101, 1552-1558.
Cooper LT. - Right from the heart: when should myocardial biopsy be performed for suspected arrhythmogenic right ventricular cardiomyopathy/dysplasia? Eur Heart J, 2008, 29, 2705-2707.
Quarta G, Muir A, Pantazis A, et al. - Familial evaluation in arrhythmogenic right ventricular cardiomyopathy: impact of genetics and revised task force criteria. Circulation, 2011, 123, 2701-2709.
Bhonsale A, James CA, Tichnell C, et al. - Incidence and predictors of Implantable cardioverter-defibrillator therapy in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy undergoing implantable cardioverter-defibrillator implantation for primary prevention. J Am Coll Cardiol, 2011, 58, 1485-1496.
Nair M, Yaduvanshi A, Kataria V, et al. - Radiofrequency catheter ablation of ventricular tachycardia in arrhythmogenic right ventricular dysplasia/cardiomyopathy using non-contact electroanatomical mapping: single-center experience with follow-up up to median of 30 months. J Interv Card Electrophysiol, 2011, 31, 141-147.
Marcus GM, Glidden D V, Polonsky B, et al. - Efficacy of antiarrhythmic drugs in arrhythmogenic right ventricular cardiomyopathy a report from the north American. ARVC registry. J Am Coll Cardiol, 2009, 54, 609-615.