Congenital heart disease combined with Arrhythmogenic Right Ventricular Cardiomyopathy A CARE compliant case report and literature review

被引:2
作者
Ren, Chutong [1 ]
Fang, Zhenfei [2 ]
Zhao, Yanshu [2 ]
Luo, Jun [2 ]
机构
[1] Cent South Univ, Xiangya Hosp 2, Dept Minimal Invas Surg, Changsha, Hunan, Peoples R China
[2] Cent South Univ, Xiangya Hosp 2, Dept Cardiol, 139 Remin Middle Rd, Changsha 410000, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
arrhythmogenic right ventricular cardiomyopathy; atrial septal defect; congenital heart disease; DYSPLASIA/CARDIOMYOPATHY; DIAGNOSIS;
D O I
10.1097/MD.0000000000020279
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rationale: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a hereditary cardiomyopathy disease discovered in 1994. Though there are advances in diagnosis of arrhythmogenic right ventricular cardiomyopathy, early diagnosis is still difficult especially when it is combined with other diseases with similar pathophysiologic changes, such as left to right shunt congenital heart disease (CHD). In this paper, we reported a case of CHD combined with ARVC. Patient concerns: The patient was referred to us for chest tightness and shortness of breath after physical activities. His cardiac MRI indicated the possibility of arrhythmogenic right ventricular cardiomyopathy. He was diagnosed with a large atrial septal defect (ASD) through ultrasound examination. Diagnosis: CHD ASD combined with arrhythmogenic right ventricular cardiomyopathy. Interventions: The patient underwent occlusion of the ASD and he was followed-up closely. His symptoms were relieved a lot and the activity tolerance was elevated. Lessons: CHD may accompany with arrhythmogenic right ventricular cardiomyopathy. Careful history collection and comprehensive examinations should be emphasized. We firmly believe that our work will be helpful for the medical practice of similar complicated cardiovascular diseases.
引用
收藏
页数:8
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