Arrhythmogenic right ventricular cardiomyopathy-dysplasiaReport as inadecuate




Arrhythmogenic right ventricular cardiomyopathy-dysplasia - Download this document for free, or read online. Document in PDF available to download.

Orphanet Journal of Rare Diseases

, 2:45

First Online: 14 November 2007Received: 09 May 2007Accepted: 14 November 2007DOI: 10.1186-1750-1172-2-45

Cite this article as: Thiene, G., Corrado, D. & Basso, C. Orphanet J Rare Dis 2007 2: 45. doi:10.1186-1750-1172-2-45

Abstract

Arrhythmogenic right ventricular cardiomyopathy-dysplasia ARVC-D is a heart muscle disease clinically characterized by life-threatening ventricular arrhythmias. Its prevalence has been estimated to vary from 1:2,500 to 1:5,000. ARVC-D is a major cause of sudden death in the young and athletes. The pathology consists of a genetically determined dystrophy of the right ventricular myocardium with fibro-fatty replacement to such an extent that it leads to right ventricular aneurysms. The clinical picture may include: a subclinical phase without symptoms and with ventricular fibrillation being the first presentation; an electrical disorder with palpitations and syncope, due to tachyarrhythmias of right ventricular origin; right ventricular or biventricular pump failure, so severe as to require transplantation. The causative genes encode proteins of mechanical cell junctions plakoglobin, plakophilin, desmoglein, desmocollin, desmoplakin and account for intercalated disk remodeling. Familiar occurrence with an autosomal dominant pattern of inheritance and variable penetrance has been proven. Recessive variants associated with palmoplantar keratoderma and woolly hair have been also reported. Clinical diagnosis may be achieved by demonstrating functional and structural alterations of the right ventricle, depolarization and repolarization abnormalities, arrhythmias with the left bundle branch block morphology and fibro-fatty replacement through endomyocardial biopsy. Two dimensional echo, angiography and magnetic resonance are the imaging tools for visualizing structural-functional abnormalities. Electroanatomic mapping is able to detect areas of low voltage corresponding to myocardial atrophy with fibro-fatty replacement. The main differential diagnoses are idiopathic right ventricular outflow tract tachycardia, myocarditis, dialted cardiomyopathy and sarcoidosis. Only palliative therapy is available and consists of antiarrhythmic drugs, catheter ablation and implantable cardioverter defibrillator. Young age, family history of juvenile sudden death, QRS dispersion ≥ 40 ms, T-wave inversion, left ventricular involvement, ventricular tachycardia, syncope and previous cardiac arrest are the major risk factors for adverse prognosis. Preparticipation screening for sport eligibility has been proven to be effective in detecting asymptomatic patients and sport disqualification has been life-saving, substantially declining sudden death in young athletes.

Electronic supplementary materialThe online version of this article doi:10.1186-1750-1172-2-45 contains supplementary material, which is available to authorized users.

Download fulltext PDF



Author: Gaetano Thiene - Domenico Corrado - Cristina Basso

Source: https://link.springer.com/







Related documents