High origin of the right coronary artery with partial anomalous pulmonary venous connection to the left superior caval vein in tetralogy of Fallot

2020 ◽  
Vol 35 (11) ◽  
pp. 3244-3247
Author(s):  
Anand K. Mishra ◽  
Vikas Kumar ◽  
Revanth Maramreddy
Keyword(s):  
Coronary Artery ◽  
Tetralogy Of Fallot ◽  
Right Coronary Artery ◽  
Caval Vein ◽  
Superior Caval Vein ◽  
The Right ◽  
Anomalous Pulmonary Venous Connection

Endocarditis of a congenital coronary fistula in a child

2017 ◽  
Vol 28 (2) ◽  
pp. 334-337 ◽  
Author(s):  
Thomas Krasemann ◽  
Ingrid M. van Beynum ◽  
Ingrid M. E. Frohn-Mulder ◽  
Michiel Dalinghaus
Keyword(s):  
Coronary Artery ◽  
Right Coronary Artery ◽  
Right Atrium ◽  
Age Group ◽  
Coronary Fistula ◽  
Vascular Plug ◽  
Caval Vein ◽  
Superior Caval Vein ◽  
Paediatric Age ◽  
The Right

AbstractEndocarditis of congenital coronary fistulas in the cardiac chambers is rare, especially in the paediatric age group. We describe the case of a 9-year-old boy with a fistula from the dilated right coronary artery to the junction of the superior caval vein to the right atrium, complicated by endocarditis. Treatment consisted of 6 weeks of antibiotics and interventional closure of the fistula 3 months later with an Amplatzer vascular plug.

Tetralogy of fallot with anomalous origin of the right coronary artery

1995 ◽  
Vol 59 (1) ◽  
pp. 229-231 ◽  
Author(s):  
R. Lawrence Moss ◽  
Carl L. Backer ◽  
Vincent R. Zales ◽  
Michael S. Florentine ◽  
Constantine Mavroudis
Keyword(s):  
Coronary Artery ◽  
Tetralogy Of Fallot ◽  
Right Coronary Artery ◽  
Anomalous Origin ◽  
The Right

Partially Anomalous Pulmonary Venous Connection to Solitary and Persistent Left Superior Caval Vein in Usual Visceroatrial Arrangement

2017 ◽  
Vol 11 (4) ◽  
pp. NP88-NP90
Author(s):  
Anoop Ayyappan ◽  
Arun Gopalakrishnan ◽  
Kapilamoorthy Tirur Raman
Keyword(s):  
Pulmonary Veins ◽  
Caval Vein ◽  
Superior Caval Vein ◽  
The Right ◽  
Anomalous Pulmonary Venous Connection

Although the occurrence of bilateral superior caval veins (SCVs) is not unusual, persistence of the left SCV with atretic right SCV is extremely uncommon in the setting of normal visceroatrial arrangement. We report such a case that was also associated with anomalous pulmonary venous connection of the right pulmonary veins to the solitary left SCV.

Echocardiographic diagnosis of totally anomalous pulmonary venous connection to the azygos vein

1999 ◽  
Vol 9 (3) ◽  
pp. 305-309 ◽  
Author(s):  
Anna Maria Musolino ◽  
Giuseppe Santoro ◽  
Bruno Marino ◽  
Roberto Formigari ◽  
Paolo Guccione ◽  
...  
Keyword(s):  
Venous Blood ◽  
Azygos Vein ◽  
Caval Vein ◽  
Superior Caval Vein ◽  
Heart Malformation ◽  
Precise Diagnosis ◽  
Right Pulmonary Artery ◽  
The Right ◽  
Anomalous Pulmonary Venous Connection ◽  
Axis View

AbstractTotally anomalous pulmonary venous connection to the azygos vein is a rare congenital heart malformation in which all the pulmonary venous blood returns anomalously to the azygos vein. Among 111 consecutive patients with totally anomalous pulmonary venous connection undergoing surgical correction at our institution between June 1982 and September 1997, this malformation was present in seven cases. By echocardiography, using a subxyphoid short-axis view at the atrial level and a modified suprasternal sagittal view, the malformation was diagnosed when the pulmonary venous confluence was traced posteriorly and superiorly relative to the right pulmonary artery and right bronchus, finally reaching reach the superior caval vein. Totally anomalous pulmonary venous connection to the azygos vein was misdiagnosed in the first two patients, both by echocardiography and angiocardiography. In the subsequent five patients, a precise diagnosis was obtained by echocardiography. Echocardiography, therefore, can be considered an accurate diagnostic tool permitting recognition of totally anomalous pulmonary venous connection to the azygos vein, and permitting corrective surgery without recourse to catheterization and angiography.

Associated Coronary Anomalies in 135 Iranian Patients with Tetralogy of Fallot

2005 ◽  
Vol 13 (4) ◽  
pp. 307-310 ◽  
Author(s):  
Manouchehr Hekmat ◽  
Sima Rafieyian ◽  
Mahnoush Foroughi ◽  
Majidi Mohammad M Tehrani ◽  
Beheshti Mahmoud Monfared ◽  
...  
Keyword(s):  
Coronary Artery ◽  
Tetralogy Of Fallot ◽  
Coronary Arteries ◽  
Right Coronary Artery ◽  
Primary Repair ◽  
Coronary Ostium ◽  
Coronary Anomalies ◽  
The Right ◽  
Single Coronary Ostium ◽  
Iranian Patients

Coronary artery anomalies are common among patients with tetralogy of Fallot. One hundred and thirty-five patients (80 males and 55 females) with tetralogy of Fallot who underwent repair between 1995 and 2002 were studied to determine the incidence of coronary anomalies in Iranian patients. Eight (5.9%) patients (4 males and 4 females) had a surgically relevant coronary artery anomaly: single coronary ostium in 5, origin of the left anterior descending artery from the right coronary artery in 2, and origin of the right coronary artery from the left coronary artery in 1. The surgical technique in 3 of these patients was repair of the ventricular septal defect with a transverse incision on the right ventricle, without damage to the coronary arteries. In another patient, an allograft aortic valve cylinder was inserted. In the other 4 patients with a single coronary ostium, placement of a limited transannular patch was adequate. Consideration of these anomalies during primary repair could decrease the risk of operation in such patients. However, it seems that the presence of anomalous coronary arteries does not affect incremental risk after surgical repair.

Anomalous origin of the right coronary artery from the pulmonary artery associated with tetralogy of Fallot: description of the pre-surgical diagnosis and surgical repair

2011 ◽  
Vol 21 (4) ◽  
pp. 468-470 ◽  
Author(s):  
Francesca R. Pluchinotta ◽  
Vladimiro Vida ◽  
Ornella Milanesi
Keyword(s):  
Coronary Artery ◽  
Pulmonary Artery ◽  
Tetralogy Of Fallot ◽  
Right Coronary Artery ◽  
Surgical Repair ◽  
Congenital Defect ◽  
Anomalous Origin ◽  
The Right

AbstractAnomalous origin of the right coronary artery from the pulmonary artery is a rare congenital defect. We describe the case of an infant with anomalous origin of the right coronary artery from the pulmonary artery in association with tetralogy of Fallot. This patient had a pre-operative echocardiographic diagnosis, which was confirmed by angiography, and later underwent a successful surgical repair.

Immediate results of bypass grafting of the territory of the right coronary artery using the 'Penza Coronary Technology'

2019 ◽  
Vol 25 (2) ◽  
pp. 137
Author(s):  
E. V. Rosseĭkin ◽  
V. V. Bazylev ◽  
E. E. Kobzev ◽  
A. B. Voevodin ◽  
P. A. Batrakov ◽  
...  
Keyword(s):  
Coronary Artery ◽  
Right Coronary Artery ◽  
Bypass Grafting ◽  
The Right
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