Isolated partial anomalous origin of a branch pulmonary artery from the descending aorta

2021 ◽  
pp. 1-4
Author(s):  
Wei-Li Liu ◽  
Ming-Chih Lin ◽  
Sheng-Ling Jan
Keyword(s):  
Pulmonary Artery ◽  
Correct Diagnosis ◽  
Diagnostic Algorithm ◽  
Pulmonary Sequestration ◽  
Arterial Supply ◽  
Anomalous Origin ◽  
Branch Pulmonary Artery ◽  
Descending Aorta ◽  
Set Up ◽  
Systemic Arterial Supply

Abstract The condition of partial anomalous origin of a branch pulmonary artery from the descending aorta could be found in several diseases and should be carefully differentiated. We report an unusual case of anomalous systemic arterial supply to normal basal segments of the left lower lung and another case of intralobar pulmonary sequestration. These two cases were treated successfully by transarterial embolisation using the Amplatzer Vascular Plug. We also set up a diagnostic algorithm to differentiate these diseases from anomalous systemic arterial supply to the pulmonary region. It is possible to make the correct diagnosis using the step-by-step diagnostic algorithm and careful interpretation of chest computed tomography angiography.

Anomalous Origin of a Branch Pulmonary Artery From the Ascending Aorta (Hemitruncus)

2018 ◽  
pp. 253-254 ◽  
Author(s):  
Michael C. Mongé ◽  
Osama Eltayeb ◽  
Andrada R. Popescu ◽  
Carl L. Backer
Keyword(s):  
Pulmonary Artery ◽  
Ascending Aorta ◽  
Anomalous Origin ◽  
Branch Pulmonary Artery

Systemic arterial supply of the right lung with venous drainage to the pulmonary arterial circuit

2011 ◽  
Vol 21 (6) ◽  
pp. 710-712 ◽  
Author(s):  
Peter Fritsch ◽  
Freyja-Maria Smolle-Juettner ◽  
Andreas Gamillscheg
Keyword(s):  
Pulmonary Artery ◽  
Venous Drainage ◽  
Left Pulmonary Artery ◽  
Scimitar Syndrome ◽  
Arterial Supply ◽  
Respiratory Problems ◽  
Right Pulmonary Artery ◽  
Pulmonary Arterial ◽  
The Right ◽  
Systemic Arterial Supply

AbstractIn a girl suffering from “Scimitar syndrome”, a rerouting of the scimitar vein was performed at the age of 6 years, but no embolisation of the aberrant systemic vessel was done. She presented with recurring respiratory problems 13 years later. An angiography revealed an invert flow from the aberrant systemic vessel via the right pulmonary artery into the left pulmonary artery. After pneumonectomy, she recovered well.

Anomalous systemic arterial supply to the left lower lobe without evidence of pulmonary sequestration

2016 ◽  
Vol 88 (5) ◽  
pp. 510-510
Author(s):  
Sameer Thakur ◽  
Siew Simg Christine Goh ◽  
Rajiv Sharma ◽  
Ashutosh Hardikar
Keyword(s):  
Lower Lobe ◽  
Pulmonary Sequestration ◽  
Left Lower Lobe ◽  
Arterial Supply ◽  
Systemic Arterial Supply

Anomalous Origin of Pulmonary Artery From Aorta: Neonatal Autologous Aortopulmonary Reconstruction

2017 ◽  
Vol 8 (4) ◽  
pp. 502-506
Author(s):  
Alexander J. Eason ◽  
Brent Shafer ◽  
Kenneth A. Murdison ◽  
Anastasios C. Polimenakos
Keyword(s):  
Pulmonary Artery ◽  
Ascending Aorta ◽  
Anomalous Origin ◽  
Aortic Tissue ◽  
Lateral Aspect ◽  
Branch Pulmonary Artery ◽  
Alternative Option ◽  
Cardiovascular Anomalies

Anomalous origin of a branch pulmonary artery (PA) from the ascending aorta is rather rare within the spectrum of congenital cardiovascular anomalies. In the scarce subset of patients with anomalous origin of right PA (RPA) from the ascending aorta originating from the lateral aspect of the distal ascending aorta, early neonatal repair by employing native aortic tissue for RPA reconstruction combined with translocation of the aorta posteriorly to the RPA can be an alternative option in the surgical armamentarium.

Abnormal origin of the left pulmonary artery from the descending aorta and heterotaxy syndrome: an undescribed phenotypic association

2021 ◽  
pp. 1-4
Author(s):  
Anne Moreau de Bellaing ◽  
Damien Bonnet ◽  
Lucile Houyel
Keyword(s):  
Pulmonary Artery ◽  
Aortic Arch ◽  
Left Pulmonary Artery ◽  
Anomalous Origin ◽  
Cardiac Anatomy ◽  
Heterotaxy Syndrome ◽  
Direct Tension ◽  
Pulmonary Atelectasis ◽  
Descending Aorta ◽  
Arterial Duct

Abstract Extensive screening in a newborn with prenatal suspicion of VACTERL syndrome identified an anomalous origin of the left pulmonary artery from the descending aorta with an arterial duct and left aortic arch, and normal intra-cardiac anatomy. Other anatomical anomalies suggested heterotaxy syndrome. At one-month-old, re-implantation of the 3.5 mm left pulmonary artery was performed by direct tension-low anastomosis. Post-operative course was complicated by severe left pulmonary atelectasis, and the patient died 20 days later.

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