scholarly journals YOUNG LADY WITH SYNCOPE- ATRIAL SEPTAL DEFECT MASQUERADING AS ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY

2021 ◽  
Vol 77 (18) ◽  
pp. 2661
Author(s):  
Sundeep Shenoy ◽  
Rajesh Janardhanan
2019 ◽  
Vol 7 (30) ◽  
pp. 58-62
Author(s):  
Lisa Marie Moore ◽  
Cihan Cevik

We report on a case of a large ostium secundum atrial septal defect (ASD) that was initially diagnosed as arrhythmogenic right ventricular cardiomyopathy (ARVC). We discuss the initial work up, diagnosis, and treatment of this patient’s ASD and explore how the pathophysiology of ARVC may mimic congenital heart disease where there is a large left-to-right shunt.


Author(s):  
Ryohsuke Narui ◽  
Seigo Yamashita ◽  
Michio Yoshitake ◽  
Tomohisa Nagoshi ◽  
Takashi Kunihara ◽  
...  

An 81-year-old woman with arrhythmogenic right ventricular cardiomyopathy underwent catheter ablation for atrial fibrillation and atrial flutter. Hypoxemia refractory to the administration of oxygen was seen after transseptal puncture. Transthoracic echocardiography revealed right to left shunt via an iatrogenic atrial septal defect (IASD) that was increased by tricuspid regurgitation flow. Her hypoxemia improved after IASD occlusion with the inflation of a venogram balloon catheter. Emergent surgical IASD closure was successfully performed. IASD after transseptal puncture for atrial fibrillation ablation infrequently causes severe complications that require emergent repair.


2014 ◽  
Vol 25 (3) ◽  
pp. 403-407
Author(s):  
Haiyan Wang ◽  
Hongyu Ding ◽  
Lei Lei ◽  
Xiaohong Zhang ◽  
Yuling Gong ◽  
...  

AbstractArrhythmogenic right ventricular cardiomyopathy is characterised by progressive, fibrofatty replacement of myocardium, and ventricular arrhythmias, and its prognosis is usually poor. Arrhythmogenic right ventricular cardiomyopathy associated with atrial septal defect is very rare, and this combination may make the diagnosis, treatment, and prognosis difficult. We present a case of a patient with this association who underwent interventional treatment with a septal defect occluder. Transcatheter closure of atrial septal defect in a patient with arrhythmogenic right ventricular cardiomyopathy is hitherto unreported. During a 3-year follow-up he remained relatively stable. We also review the cases reported in the medical literature describing this uncommon association between arrhythmogenic right ventricular cardiomyopathy and atrial septal defect or patent foramen ovale.


Sign in / Sign up

Export Citation Format

Share Document