unroofed coronary sinus
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Cureus ◽  
2021 ◽  
Author(s):  
Subrahmanya Murti Velamakanni ◽  
Gajanan Khadkikar ◽  
Shivam S Panchal ◽  
Aman Patel ◽  
Bhupesh R Shah

Author(s):  
Afsoon Fazlinezhad ◽  
Faeze Keihanian ◽  
Mostafa Ahmadi ◽  
Mohammad Tayyebi

Unroofed Coronary Sinus (UCS) is an uncommon congenital heart anomaly and the most unusual type of Atrial Septal Defect.This report presents a-71-year-old female with palpitation and dyspnea following an emotional stress, who was referred for ablation of typical atrial flutter.Finally diagnosed with a partially UCS causing a bidirectional shunt.


Author(s):  
Dustin T. Lee ◽  
Prashanth Venkatesh ◽  
Katia Bravo-Jaimes ◽  
Gentian Lluri ◽  
Eric H. Yang ◽  
...  

2021 ◽  
Author(s):  
Haruhiko Sugimori ◽  
Tatsuya Nakao ◽  
Yuki Ikegaya ◽  
Daisuke Iwahashi ◽  
Shoichi Tsuda ◽  
...  

Abstract Background: Isolated coronary sinus atrial septal defect (ASD) is defined as a coronary sinus unroofed in the terminal portion without a persistent left superior vena cava and other anomalies. This defect is rare and part of a wide spectrum of unroofed coronary sinus syndromes. Recently, several reports have described this finding. We searched the hospital’s database to determine the incidence of this defect, and to raise awareness of this condition, we discussed the findings from five patients with coronary sinus ASD who underwent surgical repair.Case presentation: The patients were three women and two men with an age range of 63–77 years. All patients underwent transthoracic echocardiography and computed tomography, and one underwent magnetic resonance imaging. In two patients, the defect was found unexpectedly intraoperatively; left-to-right shunting was apparent in the other three patients preoperatively. The pulmonary-to-systemic blood flow ratio ranged from 1.42 to 3.1 following cardiac catheterization, and oxygen saturation step-up was seen on the right side of the heart. Valvular regurgitation was seen in 4/5 patients with the mitral, tricuspid, and aortic valves involved in different combinations and to different degrees. Right atrial and ventricular dilation were seen in 4/5 patients; three patients had left atrial dilation. Three patients experienced atrial fibrillation, and one of these also experienced paroxysmal ventricular contractions. All patients underwent surgical repair, and some underwent multiple procedures. One patient who had previously undergone kidney transplantation died approximately 1 year postoperatively; the remaining four patients are currently experiencing good activities of daily living without symptoms. Conclusions: Coronary sinus ASD (Kirklin and Barratt–Boyes type IV unroofed coronary sinus syndrome) comprised 1.3% of adult congenital heart surgeries and 0.07% of adult open-heart surgeries in our hospital from 1999 to 2019. Our hospital performs cardiac surgery mainly for patients with acquired cardiac disease, and coronary sinus ASD is rare. Early diagnosis and, in symptomatic patients (especially those with blood access shunts, which may overload the heart), early surgical repair are important. The poorly prognostic case in our series is noteworthy, as similar cases have not been reported previously.


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