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
2011 ◽  
Vol 21 (4) ◽  
pp. 468-470 ◽  
Author(s):  
Francesca R. Pluchinotta ◽  
Vladimiro Vida ◽  
Ornella Milanesi

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.


2005 ◽  
Vol 101 (2) ◽  
pp. 309-310 ◽  
Author(s):  
Krishnakumar Nair ◽  
K.Mahadevan Krishnamoorthy ◽  
Jaganmohan A. Tharakan

2006 ◽  
Vol 109 (1) ◽  
pp. 125-126 ◽  
Author(s):  
Yuichi Sato ◽  
Makoto Ichikawa ◽  
Mitsuyo Masubuchi ◽  
Shunichi Yoda ◽  
Satoru Furuhashi ◽  
...  

2013 ◽  
Vol 62 (18) ◽  
pp. C228
Author(s):  
Sedat Köroğlu ◽  
Arif Suner ◽  
Cemal Tuncer ◽  
Ahmet Akcay ◽  
Alper Nacar ◽  
...  

1991 ◽  
Vol 12 (4) ◽  
pp. 558-560 ◽  
Author(s):  
G. RUSSO ◽  
C. TAMBURINO ◽  
G. LICCIARDELLO ◽  
V. CALVI ◽  
C. CINNIRELLA ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Francisco Albuquerque ◽  
Pedro de Araújo Gonçalves ◽  
Hugo Marques ◽  
António Ferreira ◽  
Pedro Freitas ◽  
...  

AbstractAnomalous origin of the right coronary artery from the opposite sinus (right-ACAOS) with interarterial course (IAC) has been associated with increased risk of sudden cardiac death (SCD). Widespread use of coronary computed tomography angiography (CCTA) has led to increased recognition of this condition, even among healthy individuals. Our study sought to examine the prevalence, anatomical characteristics, and outcomes of right-ACAOS with IAC in patients undergoing CCTA for suspected coronary artery disease (CAD). We conducted a retrospective analysis of consecutive patients referred for CCTA at one tertiary hospital from January 2012 to December 2020. Patients exhibiting right-ACAOS with IAC were analyzed for cardiac symptoms and mid-term occurrence of first MACE (cardiac death, SCD, non-fatal myocardial infarction (MI) or revascularization of the anomalous vessel). CCTAs were reviewed for anatomical high-risk features and concomitant CAD. Among 10,928 patients referred for CCTA, 28 patients with right-ACAOS with IAC were identified. Mean age was 55 ± 17 years, 64% were male and 11 (39.3%) presented stable cardiac symptoms. Most patients had at least one high risk anatomical feature. During follow-up, there were no cardiac deaths or aborted SCD episodes and only 1 patient underwent surgical revascularization of the anomalous vessel. Right-ACAOS with IAC is an uncommon finding (prevalence of 0.26%). In a contemporary population of predominantly asymptomatic patients who survived this condition well into adulthood, most patients were managed conservatively with a low event rate. Additional studies are needed to support medical follow-up as the preferred option in this setting.


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