Ablating atrial tachycardia from the right pulmonary artery: a case report

EP Europace ◽  
2019 ◽  
Vol 22 (3) ◽  
pp. 360-360
Author(s):  
Bing Han ◽  
Xian-Jin Li ◽  
Shi-Jie Li ◽  
Hao Yang ◽  
Sunny S Po
Keyword(s):  
Case Report ◽  
Pulmonary Artery ◽  
Atrial Tachycardia ◽  
Right Pulmonary Artery ◽  
The Right

Retrieval of a leadless transcatheter pacemaker from the right pulmonary artery: A case report

2020 ◽  
Author(s):  
Emanuele Romeo ◽  
Michele D'Alto ◽  
Maurizio Cappelli ◽  
Gerardo Nigro ◽  
Anna Correra ◽  
...  
Keyword(s):  
Case Report ◽  
Pulmonary Artery ◽  
Right Pulmonary Artery ◽  
The Right

scholarly journals Neonatal diagnosis of isolated absence of the right pulmonary artery: a case report and review of the literature

2018 ◽  
Vol 44 (1) ◽  
Author(s):  
Akamin Raymond ◽  
Ettore Pedretti ◽  
Giuseppina Privitera ◽  
Cristina Cicero ◽  
Giacomo Biasucci
Keyword(s):  
Case Report ◽  
Pulmonary Artery ◽  
Review Of The Literature ◽  
Neonatal Diagnosis ◽  
Right Pulmonary Artery ◽  
The Right

Spontaneous closure of right pulmonary artery-to-left atrium fistula: a case report

2016 ◽  
Vol 26 (6) ◽  
pp. 1231-1234 ◽  
Author(s):  
Neeta S. Bachani ◽  
Robin J. Pinto ◽  
Bharat V. Dalvi
Keyword(s):  
Case Report ◽  
Pulmonary Artery ◽  
Left Atrium ◽  
In Utero ◽  
Spontaneous Closure ◽  
Two Dimensional ◽  
Direct Communication ◽  
Echocardiographic Study ◽  
Right Pulmonary Artery ◽  
The Right

AbstractDirect communication between the right pulmonary artery and the left atrium is rare. We report a case that was first detected in utero and confirmed by a two-dimensional echocardiographic study performed postnatally. The patient remained asymptomatic, and hence was managed conservatively. The fistula gradually decreased in size and closed spontaneously at 15 months of age. The rarity of the case is discussed.

Anomalous Origin of the Circumflex Coronary Artery From the Right Pulmonary Artery Associated With Anomalous Aortic Origin of the Right Coronary Artery: A Case Report of Surgical Treatment

2020 ◽  
Vol 11 (4) ◽  
pp. 501-503
Author(s):  
Roman Sekelyk ◽  
Dmytro Kozhokar ◽  
Andrii Kurkevych ◽  
Oleksandra Motrechko ◽  
Illya Yemets
Keyword(s):  
Case Report ◽  
Coronary Artery ◽  
Surgical Treatment ◽  
Pulmonary Artery ◽  
Right Coronary Artery ◽  
Anomalous Origin ◽  
Circumflex Coronary Artery ◽  
Aortic Sinus ◽  
Right Pulmonary Artery ◽  
The Right

We present a patient with the extremely rare coexistence of two distinct coronary artery malformations: anomalous aortic origin of the right coronary artery from the left aortic sinus with intramural course and anomalous origin of the circumflex coronary artery from the right pulmonary artery. Surgical reimplantation of the anomalous left circumflex coronary artery to the aorta and unroofing of the intramural portion of the anomalous right coronary artery were performed.

A case report of congenital isolated absence of the right pulmonary artery: bronchofibrescopic findings and chest radiological tracings over 9 years

Respirology ◽  
2005 ◽  
Vol 10 (2) ◽  
pp. 250-253 ◽  
Author(s):  
Satoshi MIMURA ◽  
Hideo KOBAYASHI ◽  
Masaharu SHINKAI ◽  
Soichiro KANOH ◽  
Kazuo MOTOYOSHI
Keyword(s):  
Case Report ◽  
Pulmonary Artery ◽  
Right Pulmonary Artery ◽  
The Right
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