Myocardial fibrosis detection in arrhythmogenic right ventricular dysplasia/cardiomyopathy by 3. 0T magnetic resonance imaging  

Myocardial fibrosis detection in arrhythmogenic right ventricular dysplasia/cardiomyopathy by 3. 0T magnetic resonance imaging

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作  者:黄俊 吴书林 刘辉 方咸宏 谭绍恒 

机构地区:[1]Department of Cardiology,Guangdong Provincial Cardiovascular Institute,Guangdong General Hospital [2]Guangdong Academy of Medical Sciences [3]Department of Radiology,Guangdong Provincial Cardiovascular Institute,Guangdong General Hospital,Guangdong Academy of Medical Sciences [4]Department of Radiology,Guangdong Provincial Cardiovascular Institute,Guangdong General Hospital

出  处:《South China Journal of Cardiology》2010年第2期69-73,共5页岭南心血管病杂志(英文版)

摘  要:Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is characterized by fibro-fatty replacement of the right ventricle.However,the feasibility and significance of myocardial fibrosis detec-ted by delayed enhancement (DE) using 3.0T magnetic resonance imaging (MRI) in.ARVD /C is seldomly studied.Methods Twenty-seven consecutive patients were prospectively evaluated for ARVD /C.Magnetic reso-nance imaging was performed on a 3.0T scanner.Ten minutes after intravenous administration of 0.2 mmol /kg of gadodiamide,DE-MRI was obtained.Diagnosis of ARVD /C was based upon the Task Force criteria and in-cluded MRI findings.Results Seventeen(59% ) of 27 patients met the Task Force criteria for ARVD /C.Right ven-tricle DE was found in all (100% ) ARVD /C patients compared with none (0%) of the 10 patients without ARVD /C (P <0.001) .Additional left ventricular DE was found in 8/17 ARVD/C patients while without left ventricular mor-phological and functional abnormalities detected by echocardiography or MRI.Conclusions DE using 3.0T MRI could effectively detect myocardial fibrosis in the right and left ventricular myocardium in ARVD /C patients.Detection of myocardial fibrosis may have an important clinical significance in ARVD/C diagnosis.Histological left ventricle in-volvement may be easily missed by echocardiography.Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is characterized by fibro-fatty replacement of the right ventricle.However,the feasibility and significance of myocardial fibrosis detec-ted by delayed enhancement (DE) using 3.0T magnetic resonance imaging (MRI) in.ARVD /C is seldomly studied.Methods Twenty-seven consecutive patients were prospectively evaluated for ARVD /C.Magnetic reso-nance imaging was performed on a 3.0T scanner.Ten minutes after intravenous administration of 0.2 mmol /kg of gadodiamide,DE-MRI was obtained.Diagnosis of ARVD /C was based upon the Task Force criteria and in-cluded MRI findings.Results Seventeen(59% ) of 27 patients met the Task Force criteria for ARVD /C.Right ven-tricle DE was found in all (100% ) ARVD /C patients compared with none (0%) of the 10 patients without ARVD /C (P <0.001) .Additional left ventricular DE was found in 8/17 ARVD/C patients while without left ventricular mor-phological and functional abnormalities detected by echocardiography or MRI.Conclusions DE using 3.0T MRI could effectively detect myocardial fibrosis in the right and left ventricular myocardium in ARVD /C patients.Detection of myocardial fibrosis may have an important clinical significance in ARVD/C diagnosis.Histological left ventricle in-volvement may be easily missed by echocardiography.

关 键 词:3. 0T magnetic resonance delayed enhancement magnetic resonance imaging arrhythmogenic right ven- tricular dysplasia/cardiomyopathy ( ARVD /C) myocardial fibrosis 

分 类 号:R541.7[医药卫生—心血管疾病]

 

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