scholarly journals Breaking the Rules: Left Common Carotid Artery from the Main Pulmonary Artery in an Infant with a Vascular Ring

CASE ◽  
2021 ◽  
Author(s):  
Stephan Juergensen ◽  
Emilio Quezada ◽  
Norman H. Silverman ◽  
Jeffrey G. Gossett ◽  
Peter Kouretas ◽  
...  
2004 ◽  
Vol 26 (5) ◽  
pp. 707-709 ◽  
Author(s):  
N. Kaushik ◽  
Z. Saba ◽  
H. Rosenfeld ◽  
H.T. Patel ◽  
K. Martin ◽  
...  

2019 ◽  
Vol 29 (3) ◽  
pp. 422-424
Author(s):  
Kumiyo Matsuo ◽  
Hisaaki Aoki ◽  
Futoshi Kayatani

AbstractAn isolated left common carotid artery is very rare, and only 13 cases have been reported thus far. All those cases were accompanied by a right aortic arch and aberrant left subclavian artery, and the connecting vessel between the pulmonary artery and left common carotid artery was thought to be ductal tissue. However, there have been no reports that have followed the natural closure of this vessel. We present a case in whom we could observe the closing process of this vessel at the connection between the left common carotid artery and main pulmonary artery in association with a tetralogy of Fallot.


2016 ◽  
Vol 2016 ◽  
pp. 1-4 ◽  
Author(s):  
Onyekachukwu Osakwe ◽  
Blaise Jones ◽  
Russel Hirsch

Case Report. Isolated carotid artery originating from the pulmonary trunk is an exceedingly rare anomalous origin of head and neck vessels. We present this finding, along with a persistent embryonic trigeminal artery, in a male infant with multiple cardiac defects and other congenital anomalies associated with CHARGE syndrome. After extensive investigations, cardiac catheterization revealed the anomalous left common carotid artery arising from the cranial aspect of the main pulmonary artery. There was retrograde flow in this vessel, resulting from the lower pulmonary pressure, essentially stealing arterial supply from the left anterior cerebral circulation. The persistent left-sided trigeminal artery provided collateral flow from the posterior circulation to the left internal carotid artery territory, allowing for safe ligation of the anomalous origin of the left common carotid artery, thereby reversing the steal of arterial blood flow into the pulmonary circulation and resulting in a net improvement of cerebral perfusion.Conclusion. The possibility of this vascular anomaly should be considered in all infants with CHARGE syndrome. Surgical repair or ligation should be tailored to the specific patient circumstances, following a careful delineation of all sources of cerebral perfusion.


2015 ◽  
Vol 25 (6) ◽  
pp. 1193-1196 ◽  
Author(s):  
Alireza Ahmadi ◽  
Mohammadreza Sabri ◽  
Bahar Dehghan

AbstractA 20-day-old girl was referred to our clinic for systolic murmur, cyanosis, and dyspnoea with feeding. Echocardiography revealed an atretic aortic valve. CT angiography scan revealed that the left common carotid artery originated from the distal main pulmonary artery. The plan was patent ductus artriosus stenting and bilateral pulmonary artery banding and then follow-up for any possible future intervention.


2009 ◽  
Vol 4 ◽  
pp. S171-S172
Author(s):  
Vu Tuan Nguyen ◽  
Thanh Hai Phan ◽  
Duc Huy Dinh ◽  
Kim Phuong Phan ◽  
Nguyen Vinh Pham

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