scholarly journals Anomalous origin of the right coronary artery from the pulmonary artery. Two case reports

2014 ◽  
Vol 66 (3) ◽  
pp. 283-286 ◽  
Author(s):  
K. Hakim ◽  
R. Boussaada ◽  
I. Hamdi ◽  
Fatma Ouarda
Keyword(s):  
Coronary Artery ◽  
Pulmonary Artery ◽  
Right Coronary Artery ◽  
Case Reports ◽  
Anomalous Origin ◽  
The Right

scholarly journals A right coronary artery aneurysm 16 years after surgical repair of anomalous origin of the right coronary artery from the pulmonary artery

2019 ◽  
Vol 29 (1) ◽  
pp. 157-158
Author(s):  
Akira Furutachi ◽  
Kojiro Furukawa ◽  
Aiko Komatsu ◽  
Eijiro Nogami
Keyword(s):  
Coronary Artery ◽  
Pulmonary Artery ◽  
Right Coronary Artery ◽  
Surgical Repair ◽  
Artery Aneurysm ◽  
Anomalous Origin ◽  
Artery Graft ◽  
Long Term Follow Up ◽  
The Right

Abstract Anomalous origin of the right coronary artery (RCA) from the pulmonary artery is a very rare congenital heart disease, and several reports have described long-term events after surgery. We report the case of a 46-year-old woman who underwent reimplantation of the RCA for anomalous origin of the right coronary artery from the pulmonary artery 16 years ago. An RCA aneurysm gradually developed and dilated over time, and we resected the aneurysm and also grafted the right gastroepiploic artery graft to the distal RCA. Careful long-term follow-up is required to avoid overlooking such a rare but life-threatening complication after surgical repair of anomalous origin of the right coronary artery from the pulmonary artery.

scholarly journals Anomalous origin of the right coronary artery from the pulmonary artery: a rare finding in an asymptomatic man

2011 ◽  
Vol 12 (11) ◽  
pp. 884-884 ◽  
Author(s):  
J. A. Petersen ◽  
C. A. Karlo ◽  
H. Alkadhi ◽  
O. Gaemperli ◽  
P. Biaggi
Keyword(s):  
Coronary Artery ◽  
Pulmonary Artery ◽  
Right Coronary Artery ◽  
Anomalous Origin ◽  
Rare Finding ◽  
The Right

scholarly journals Anomalous origin of the right coronary artery from the pulmonary artery diagnosed in an adult: A case report

2014 ◽  
Vol 10 (3) ◽  
pp. 111-114 ◽  
Author(s):  
Keisuke Nakabayashi ◽  
Hisayuki Okada ◽  
Yuji Iwanami ◽  
Ryo Sugiura ◽  
Toshiaki Oka
Keyword(s):  
Case Report ◽  
Coronary Artery ◽  
Pulmonary Artery ◽  
Right Coronary Artery ◽  
Anomalous Origin ◽  
The Right

Anomalous Origin of the Right Coronary Artery from the Pulmonary Artery

CHEST Journal ◽  
1973 ◽  
Vol 63 (2) ◽  
pp. 294-296 ◽  
Author(s):  
George S. Eugster ◽  
Philip B. Oliva
Keyword(s):  
Coronary Artery ◽  
Pulmonary Artery ◽  
Right Coronary Artery ◽  
Anomalous Origin ◽  
The Right

Case Report Anomalous Origin of the Right Coronary Artery from the Pulmonary Artery

1981 ◽  
Vol 281 (3) ◽  
pp. 152-156 ◽  
Author(s):  
Joseph Salomon ◽  
Romulo Baltazar ◽  
Morton M. Mower ◽  
Stanford Goldman
Keyword(s):  
Case Report ◽  
Coronary Artery ◽  
Pulmonary Artery ◽  
Right Coronary Artery ◽  
Anomalous Origin ◽  
The Right

Anomalous Origin of the Right Coronary Artery From the Pulmonary Artery: Unusual Presentation in an Adult

2012 ◽  
Vol 3 (2) ◽  
pp. 271-272
Author(s):  
Salah Eldien Altarabsheh ◽  
Sabrina D. Phillips ◽  
William C. Oliver ◽  
Harold M. Burkhart
Keyword(s):  
Coronary Artery ◽  
Pulmonary Artery ◽  
Adult Patient ◽  
Right Coronary Artery ◽  
Unusual Presentation ◽  
Anomalous Origin ◽  
The Right

We report an anomalous right coronary artery origin from the pulmonary artery presenting in an adult patient.

scholarly journals Association of Anomalous Origin of the Right Coronary Artery from the Pulmonary Artery with Aortopulmonary Window. Two case report

2020 ◽  
Vol 5 (6) ◽  
Keyword(s):  
Coronary Artery ◽  
Pulmonary Artery ◽  
Right Coronary Artery ◽  
Coronary Flow ◽  
Anomalous Origin ◽  
Congenital Defects ◽  
Aortopulmonary Window ◽  
Rare Entity ◽  
Asymptomatic Patients ◽  
The Right

Anomalous origin of the right coronary artery from the pulmonary artery (ARCAPA) is a rare entity. Brooks described first cases in 1885. Only 25% to 30% % of cases are associated with congenital defects such as aortopulmonary window and tetralogy of Fallot. It is recommended the reimplantation of the right coronary artery in the Aorta, with redistribution of coronary flow avoiding the signs of ischemia or other complications even when the diagnosis is done in asymptomatic patients. This is the report of two infants with who debuted with murmur and signs of heart failure. ARCAPA and Pulmonary Aortic Window were diagnosed and they were surgically corrected through intrapulmonary tunneling with a favorable evolution.

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