Concordant Ventriculoarterial Connections With Parallel Arterial Trunks, Divided Left Atrium, and Juxtaposed Atrial Appendages

2012 ◽  
Vol 3 (2) ◽  
pp. 260-263
Author(s):  
Sachin Talwar ◽  
Vinitha Vishambaran Nair ◽  
Shiv Kumar Choudhary ◽  
Gurpreet Singh Gulati ◽  
Robert H. Anderson ◽  
...  

We describe a patient with concordant ventriculoarterial connections with parallel arterial trunks, divided left atrium (cor triatriatum sinister), ventricular septal defect, bilateral superior caval veins, and juxtaposed atrial appendages. The aorta was anterior and left sided. We discuss the morphological features of this rare condition, and the diagnostic dilemma it produced.

2020 ◽  
Vol 18 (1) ◽  
pp. 28-30
Author(s):  
Zanda Grīnberga ◽  
Pauls Sīlis ◽  
Elīna Ligere ◽  
Ingūna Lubaua ◽  
Inta Bergmane ◽  
...  

SummaryCor triatriatum sinister is a rare congenital cardiac anomaly that has been identified in 0.1% of children with congenital heart disease. It is defined as a fibromuscular membrane that divides the left atrium into two chambers: a superior (proximal) that in most cases receives drainage from the pulmonary veins and an inferior (distal) chamber that communicates with the mitral valve and the left atrium. Cor triatriatum sinister can be an isolated lesion (approximately 25% of cases), but in many cases it is associated with other congenital cardiovascular anomalies, the most common one being – atrial septal defect(3). Symptoms in patients with cor triatriatum sinister are related to obstruction of pulmonary venous drainage, pressure loading of the right side of the heart and congestive cardiac failure. Depending on the severity of the obstruction and presence of associated cardiac anomalies it can be diagnosed at any age. Diagnosis is usually achieved by echocardiography in early infancy. Elective treatment method is surgical excision of the membrane. Here we present a pediatric patient (4 months old) presenting in cardiogenic shock with a successful correction of isolated cor triatriatum sinister. To confirm diagnosis and success of surgical repair, transthoracic and transesophageal echocardiography were used.


2020 ◽  
Vol 110 (4) ◽  
pp. 1380-1386
Author(s):  
Hamood N. Al Kindi ◽  
Mahmoud Shehata ◽  
Ayman M. Ibrahim ◽  
Mohamed Roshdy ◽  
Walid Simry ◽  
...  

CASE ◽  
2017 ◽  
Vol 1 (4) ◽  
pp. 141-146
Author(s):  
James Lambert ◽  
Erwin Oechslin ◽  
Wendy Tsang ◽  
Mark D. Osten ◽  
Paaladinesh Thavendiranathan

1993 ◽  
Vol 3 (1) ◽  
pp. 57-59 ◽  
Author(s):  
Mario Cazzaniga ◽  
Manuel Casanova Gómez ◽  
Walquiria Domínguez de Melo

SummaryWe describe the unusual association of a divided left atrium (cor triatriatum) with an atrioventricular septal defect with separate atrioventricular orifices in an eight-year-old asymptomatic girl. The diagnosis had been made by cross-sectional echocardiography combined with Doppler technology and color-flow mapping. These methods together demonstrate both the anatomic and hemodynamic findings.


2011 ◽  
Vol 13 (6) ◽  
pp. 463-466 ◽  
Author(s):  
Shu Nakao ◽  
Ryou Tanaka ◽  
Lina Hamabe ◽  
Shuji Suzuki ◽  
Huai-Che Hsu ◽  
...  

Author(s):  
Changqing Gao ◽  
Ming Yang ◽  
Cangsong Xiao ◽  
Huajun Zhang ◽  
Gang Wang

Cor triatriatum sinister (CTS) is a rare congenital cardiac anomaly and is mainly corrected through conventional surgery through sternotomy. We described our successful novel surgical technique of totally robotic correction of CTS in one case of CTS with concomitant repair of atrial septal defect using da Vinci SI Surgical System (Intuitive Surgical, Inc, Sunnyvale, CA USA) with excellent surgical outcome. We conclude that robotic correction of CTS is a feasible and safe alternative to conventional surgical technique.


2013 ◽  
Vol 167 (4) ◽  
pp. e95-e96 ◽  
Author(s):  
Giuseppe Damiano Sanna ◽  
Pier Sergio Saba ◽  
Antonella Canu ◽  
Federica Decandia ◽  
Giovanni Di Girolamo ◽  
...  

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