scholarly journals Perforation of the right pulmonary artery branch to the right middle lobe with a Swan-Ganz catheter during cardiopulmonary bypass, resulting in endobronchial hemorrhage

1991 ◽  
Vol 102 (5) ◽  
pp. 807-808 ◽  
Author(s):  
Andrew S. Olearchyk ◽  
Annapoorna Varada
Keyword(s):  
Cardiopulmonary Bypass ◽  
Pulmonary Artery ◽  
Middle Lobe ◽  
Pulmonary Artery Branch ◽  
Right Pulmonary Artery ◽  
Right Middle Lobe ◽  
The Right ◽  
Artery Branch

Bronchial atresia associated with epibronchial right pulmonary artery and aberrant right middle lobe artery.

1998 ◽  
Vol 71 (842) ◽  
pp. 217-220 ◽  
Author(s):  
S F Ko ◽  
T Y Lee ◽  
C L Kao ◽  
S H Ng ◽  
Y L Wan ◽  
...  
Keyword(s):  
Pulmonary Artery ◽  
Middle Lobe ◽  
Right Pulmonary Artery ◽  
Right Middle Lobe ◽  
Bronchial Atresia

Anomalous Connection of Left Circumflex Artery to Pulmonary Artery

2002 ◽  
Vol 10 (4) ◽  
pp. 334-335 ◽  
Author(s):  
Seyed Hamid Mirkhani ◽  
Morteza Delavarkhan ◽  
Homeyra Bayat ◽  
Mahdi Sanatkar
Keyword(s):  
Cardiopulmonary Bypass ◽  
Coronary Angiography ◽  
Pulmonary Artery ◽  
Chest Discomfort ◽  
Circumflex Artery ◽  
Left Circumflex Artery ◽  
Right Pulmonary Artery ◽  
The Right ◽  
Successful Repair

A 52-year-old woman was evaluated for chest discomfort and dyspnea on exertion. Coronary angiography demonstrated an anomalous connection between the left circumflex artery and the right pulmonary artery. Successful repair was achieved under cardiopulmonary bypass, and the patient became completely symptom-free.

scholarly journals Pulmonary artery sling in a symptomatic newborn

2021 ◽  
Vol 13 (3) ◽  
pp. 254-257
Author(s):  
İlker Mercan ◽  
Muhammet Akyuz ◽  
Onur Işık
Keyword(s):  
Pulmonary Artery ◽  
Respiratory Symptoms ◽  
Main Pulmonary Artery ◽  
Left Pulmonary Artery ◽  
Uneventful Recovery ◽  
Pulmonary Artery Sling ◽  
Right Pulmonary Artery ◽  
Pulmonary Arterial ◽  
The Right ◽  
Artery Branch

Pulmonary arterial sling (PAS) is a relatively rare congenital anomaly in which left pulmonary artery branch originates abnormally from the right pulmonary artery, eventually resulting with respiratory symptoms, due to airway obstruction. In this report, we present a PAS in a neonate who showed progressive respiratory distress in the second week following delivery. At 25 days of age, the patient underwent total surgical correction of the anomaly, during which left pulmonary artery reimplantation to main pulmonary artery without the use of cardiopulmonary bypass was employed. Following an uneventful recovery, the patient was discharged eighteen days after surgery.

Unusual Case of Common Arterial Trunk With Atresia of the Right Pulmonary Artery and Aortopulmonary Collaterals

2020 ◽  
Vol 11 (4) ◽  
pp. 534-536
Author(s):  
Deborah Kozik ◽  
Philip Dydynski ◽  
Erle Austin ◽  
Bahaaldin Alsoufi
Keyword(s):  
Pulmonary Artery ◽  
Unusual Case ◽  
Ascending Aorta ◽  
Intracardiac Repair ◽  
Common Arterial Trunk ◽  
Arterial Trunk ◽  
Right Pulmonary Artery ◽  
Aortopulmonary Collaterals ◽  
The Right ◽  
Artery Branch

We describe a two-year-old African girl with late diagnosis of unusual case of common arterial trunk with two separate pulmonary artery branch origins from the ascending aorta, hypoplastic right pulmonary artery that becomes atretic and reconstitutes at hilum, and three aortopulmonary collaterals providing right lung blood supply. She underwent single-stage intracardiac repair and unifocalization of collaterals.

Anomalous origin of the right pulmonary artery from the ascending aorta: repair without cardiopulmonary bypass

1989 ◽  
Vol 23 (3) ◽  
pp. 309-313 ◽  
Author(s):  
Carlo Fucci ◽  
Duccio C. di Carlo ◽  
Roberto Di Donato ◽  
Bruno Marino ◽  
Giuseppe Calcaterra ◽  
...  
Keyword(s):  
Cardiopulmonary Bypass ◽  
Pulmonary Artery ◽  
Ascending Aorta ◽  
Anomalous Origin ◽  
Right Pulmonary Artery ◽  
The Right

Fistula between the right pulmonary artery and the left atrium—an unusual cause of cyanotic heart disease

1995 ◽  
Vol 5 (1) ◽  
pp. 85-87 ◽  
Author(s):  
Kjell Saatvedt ◽  
Gunnar Stake ◽  
Harald Lindberg
Keyword(s):  
Congenital Anomaly ◽  
Heart Disease ◽  
Cardiopulmonary Bypass ◽  
Pulmonary Artery ◽  
Left Atrium ◽  
Cyanotic Heart Disease ◽  
Postoperative Course ◽  
Rare Congenital Anomaly ◽  
Right Pulmonary Artery ◽  
The Right

AbstractA fistula from the pulmonary artery to the left atrium is a very rare congenital anomaly. The communication, almost exclusively arising from the right pulmonary artery, may give rise to a variety of symptoms with cyanosis as the predominant sign. To our knowledge only seven neonates have been reported with this anomaly, and five of them died postoperatively. We present another two neonates with such a fistula which was closed by simple ligation using a transsternal approach and cardiopulmonary bypass. Both patients had an uneventful postoperative course and are alive and well at the age of two and three years, respectively.

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