Anomalous origin of innominate artery from right pulmonary artery in DiGeorge syndrome

2001 ◽  
Vol 71 (6) ◽  
pp. 2043-2044 ◽  
Author(s):  
Kagami Miyaji ◽  
Robert L Hannan ◽  
Redmond P Burke
Keyword(s):  
Pulmonary Artery ◽  
Digeorge Syndrome ◽  
Innominate Artery ◽  
Anomalous Origin ◽  
Right Pulmonary Artery

scholarly journals Anomalous origin of right pulmonary artery from innominate artery: Repair using pulmonary artery pedicled flap plasty

2017 ◽  
Vol 10 (3) ◽  
pp. 278
Author(s):  
Roy Varghese ◽  
Jai Ganesh ◽  
Jeeva Nandam ◽  
Sujathaa Ravikumar ◽  
Sivakumar Kothandam
Keyword(s):  
Pulmonary Artery ◽  
Innominate Artery ◽  
Pedicled Flap ◽  
Anomalous Origin ◽  
Right Pulmonary Artery

Anomalous origin of right pulmonary artery from ascending aorta - A case report

2019 ◽  
Vol 10 (3) ◽  
pp. 13-14
Author(s):  
Manohar B Kachare ◽  
◽  
Vijay C Nalpe ◽  
Ravi Raval ◽  
◽  
...  
Keyword(s):  
Case Report ◽  
Pulmonary Artery ◽  
Ascending Aorta ◽  
Anomalous Origin ◽  
Right Pulmonary Artery

scholarly journals A Rare Case of Adult Aortopulmonary Window Combined with Anomalous Origin of the Right Pulmonary Artery from the Aorta Leading to Eisenmenger Syndrome

2021 ◽  
Vol 49 (1) ◽  
pp. 030006052098465
Author(s):  
Mingyue Cui ◽  
Binfeng Xia ◽  
Heru Wang ◽  
Haihui Liu ◽  
Xia Yin
Keyword(s):  
Pulmonary Artery ◽  
Rare Case ◽  
Congenital Heart ◽  
Respiratory Tract Infections ◽  
Anomalous Origin ◽  
Aortopulmonary Window ◽  
Eisenmenger Syndrome ◽  
Right Pulmonary Artery ◽  
The Right ◽  
Tract Infections

Aortopulmonary window is a rare congenital heart disease that can increase pulmonary vascular resistance, exacerbate left-to-right shunt and lead to heart failure and respiratory tract infections. Most patients die during childhood. We report a 53-year-old male patient with a large aortopulmonary window combined with anomalous origin of the right pulmonary artery from the aorta, with Eisenmenger syndrome and without surgery.

Anomalous origin of the right pulmonary artery from the ascending aorta: Diagnosis by magnetic resonance imaging

1995 ◽  
Vol 18 (2) ◽  
pp. 118-121 ◽  
Author(s):  
Tae Kyoung Kim ◽  
Yeon Hyoen Choe ◽  
Hak Soo Kim ◽  
Jae Kon Ko ◽  
Young Tak Lee ◽  
...  
Keyword(s):  
Magnetic Resonance Imaging ◽  
Magnetic Resonance ◽  
Pulmonary Artery ◽  
Ascending Aorta ◽  
Anomalous Origin ◽  
Resonance Imaging ◽  
Right Pulmonary Artery ◽  
The Right

Total anomalous origin of the coronary circulation from the right pulmonary artery

2008 ◽  
Vol 17 (4) ◽  
pp. 246-249 ◽  
Author(s):  
Fabio Tavora ◽  
Allen Burke ◽  
Robert Kutys ◽  
Ling Li ◽  
Renu Virmani
Keyword(s):  
Pulmonary Artery ◽  
Coronary Circulation ◽  
Anomalous Origin ◽  
Right Pulmonary Artery ◽  
The Right

Prenatal diagnosis of anomalous origin of the right pulmonary artery from the ascending aorta

2002 ◽  
Vol 12 (2) ◽  
pp. 186-188 ◽  
Author(s):  
Mi-Jin Jung ◽  
Shi-Joon Yoo
Keyword(s):  
Prenatal Diagnosis ◽  
Pulmonary Artery ◽  
Ascending Aorta ◽  
Anomalous Origin ◽  
Fetal Ultrasound ◽  
Cardiac Screening ◽  
Rare Anomaly ◽  
Right Pulmonary Artery ◽  
The Right

We report a case of anomalous origin of the right pulmonary artery from the ascending aorta that was diagnosed by fetal ultrasound at 21 weeks of gestation. The clue to the diagnosis was present in the three-vessel view, this being one of the views that we use for fetal cardiac screening. The anomaly was corrected surgically at 11 days of age. We discuss the importance of prenatal diagnosis in the management of this rare anomaly.

Intramural Aortic Course Should Always Be Considered for Anomalous Origin of the Left Coronary Artery From the Right Pulmonary Artery

2019 ◽  
Vol 10 (4) ◽  
pp. 508-512
Author(s):  
Vishal Agrawal ◽  
Nikunj Vaidhya ◽  
Mrinal Patel ◽  
Amit Mishra ◽  
Dinesh Patel
Keyword(s):  
Coronary Artery ◽  
Pulmonary Artery ◽  
Left Coronary Artery ◽  
Anomalous Origin ◽  
Preoperative Imaging ◽  
Rare Entity ◽  
Right Pulmonary Artery ◽  
The Right

Anomalous origin of the left coronary artery (LCA) from the right pulmonary artery (ALCARPA) is an extremely rare subset of an already rare entity, anomalous origin of the LCA from the pulmonary artery. Whenever it is diagnosed preoperatively, one should be extremely vigilant about the potential intramural course of the descending part of the LCA in the aorta. Preoperative imaging frequently fails to delineate this intramural course. We report our experience with one such case where we had accidentally injured the LCA during dissection from the right pulmonary artery. Although it was successfully managed, it reinforces our aforementioned point concerning the importance of vigilance in seeking to identify intramurality as a component of this anomaly of coronary artery origin.

An unusual cause of refractory persistent pulmonary hypertension of the newborn: anomalous origin of one pulmonary artery

2013 ◽  
Vol 24 (3) ◽  
pp. 543-545
Author(s):  
Nilufer Guzoglu ◽  
Fatma Nur Sari ◽  
Nahide Altug
Keyword(s):  
Pulmonary Hypertension ◽  
Pulmonary Artery ◽  
Innominate Artery ◽  
Persistent Pulmonary Hypertension ◽  
Anomalous Origin ◽  
Cardiac Malformation ◽  
Mortality And Morbidity ◽  
Congenital Cardiac Malformation

AbstractPersistent pulmonary hypertension of the newborn is a source of considerable mortality and morbidity. Anomalous origin of one pulmonary artery, an uncommon congenital cardiac malformation, is a rare cause of persistent pulmonary hypertension. Here, we report the case of a patient with an anomalous origin of one pulmonary artery from the innominate artery who presented with persistent pulmonary hypertension refractory to treatment.

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