Abstract
The authors describe what is, to their knowledge, the first reported case of the anomalous origin of an internal carotid artery from the pulmonary artery. An otherwise asymptomatic 6-year-old girl, who presented with headaches and hypertension, underwent a comprehensive workup that revealed extensive meningeal and cerebral artery anastomoses to the left internal carotid artery - itself arising from the origin of the left pulmonary artery. This unique anatomical anomaly, caused by a disturbed pattern of aortic arch regression, resulted in a right-to-left vascular shunt into the pulmonary artery and a disturbance of intracranial artery flow patterns, complicating the management options.
Original language | English (US) |
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Pages (from-to) | 207-211 |
Number of pages | 5 |
Journal | Journal of Neurosurgery: Pediatrics |
Volume | 2 |
Issue number | 3 |
DOIs | |
State | Published - Sep 1 2008 |
Keywords
- Aortic arch
- Internal carotid artery
- Pulmonary artery
ASJC Scopus subject areas
- Clinical Neurology
- Surgery
- Pediatrics, Perinatology, and Child Health