MR imaging of arrhythmogenic right ventricular dysplasia: What the radiologist needs to know
Autor: | Arthur Varoquaux, Vincent Vidal, A. Tavano, Jean-Yves Gaubert, Boris Maurel, Alexis Jacquier, Jean-Michel Bartoli, P. Cassagneau, Guy Moulin |
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Rok vydání: | 2015 |
Předmět: |
Adult
Male medicine.medical_specialty Cardiomyopathy Diastole Sudden death Diagnosis Differential Internal medicine medicine Humans Radiology Nuclear Medicine and imaging Child Cardiac MRI Arrhythmogenic Right Ventricular Dysplasia Ejection fraction Radiological and Ultrasound Technology medicine.diagnostic_test business.industry Magnetic resonance imaging General Medicine Middle Aged medicine.disease Magnetic Resonance Imaging Arrhythmogenic right ventricular dysplasia Cardiac Imaging Techniques medicine.anatomical_structure Ventricle Cardiology Female Radiology Differential diagnosis business |
Zdroj: | Diagnostic and Interventional Imaging. 96:449-460 |
ISSN: | 2211-5684 |
DOI: | 10.1016/j.diii.2014.07.009 |
Popis: | Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is an inherited heart muscle disease that predominantly affects the right ventricle. Clinical manifestations are related to severe ventricular arrhythmia that may lead to sudden death, mostly in young patients. Magnetic resonance imaging (MRI), included in the new diagnostic criteria since 2010, aims to detect segmental and global wall motion abnormalities, reduced ejection fraction, right ventricular dilatation and right ventricular diastolic/systolic dysfunction. An MRI assessment of the right ventricle is often challenging, partly because the MRI diagnostic criteria have some limitations, and also because it requires a significant learning curve due to the low prevalence of the disease. Therefore, this article aims to review the pathophysiology of the disease, the cardiac MRI protocol, images of the various stages of this affection as well as the differential diagnosis. |
Databáze: | OpenAIRE |
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