Anomalous Origin of the Left Common Carotid Artery from the Main Pulmonary Artery: A Rare Association in an Infant with CHARGE Syndrome

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 asso...

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Main Authors: Onyekachukwu Osakwe (Author), Blaise Jones (Author), Russel Hirsch (Author)
Format: Book
Published: Hindawi Limited, 2016-01-01T00:00:00Z.
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100 1 0 |a Onyekachukwu Osakwe  |e author 
700 1 0 |a Blaise Jones  |e author 
700 1 0 |a Russel Hirsch  |e author 
245 0 0 |a Anomalous Origin of the Left Common Carotid Artery from the Main Pulmonary Artery: A Rare Association in an Infant with CHARGE Syndrome 
260 |b Hindawi Limited,   |c 2016-01-01T00:00:00Z. 
500 |a 2090-6803 
500 |a 2090-6811 
500 |a 10.1155/2016/2064937 
520 |a 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. 
546 |a EN 
690 |a Pediatrics 
690 |a RJ1-570 
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786 0 |n Case Reports in Pediatrics, Vol 2016 (2016) 
787 0 |n http://dx.doi.org/10.1155/2016/2064937 
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787 0 |n https://doaj.org/toc/2090-6811 
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