Direct Communication between the Pulmonary Artery and Left Atrium

1982 ◽  
Vol 16 (2) ◽  
pp. 157-160 ◽  
Author(s):  
H. Arendrup
Keyword(s):  
Pulmonary Artery ◽  
Left Atrium ◽  
Direct Communication

scholarly journals Direct communication of the right pulmonary artery with the left atrium

1972 ◽  
Vol 64 (1) ◽  
pp. 38-44 ◽  
Author(s):  
Tadaaki Abe ◽  
Ryosei Kuribayashi ◽  
Mamoru Sato ◽  
Shigeo Nieda
Keyword(s):  
Pulmonary Artery ◽  
Left Atrium ◽  
Direct Communication ◽  
Right Pulmonary Artery ◽  
The Right

scholarly journals Direct Communication with Fistula between the Left Main Pulmonary Artery and the Left Atrium: A Case Report

2012 ◽  
Vol 66 (3) ◽  
pp. 235
Author(s):  
Yeon-Jee Ko ◽  
Song Soo Kim ◽  
Jin-Hwan Kim ◽  
Jae-Hyeong Park ◽  
Jae-Hwan Lee
Keyword(s):  
Case Report ◽  
Pulmonary Artery ◽  
Left Atrium ◽  
Main Pulmonary Artery ◽  
Left Main ◽  
Direct Communication

Unexpected Cause of Cyanosis and Dyspnea in an Adult: Direct Communication of the Right Pulmonary Artery and Left Atrium

2014 ◽  
Vol 97 (5) ◽  
pp. 1782-1784
Author(s):  
Ismail Dogu Kilic ◽  
Yusuf I. Alihanoglu ◽  
Nevzat Karabulut ◽  
Fırat Durna ◽  
Bilgin Emrecan
Keyword(s):  
Pulmonary Artery ◽  
Left Atrium ◽  
Direct Communication ◽  
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.

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