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MR angiographic findings of aberrant right subclavian artery with agenesis of the left common carotid artery and anomalous origin of the vertebral arteries

Congenital aortic arch anomalies and variants have been extensively characterized in the medical literature. Proper identification of these anomalies is important when surgical or percutaneous interventions are indicated. We present a case of a 48-year old male who presented to the emergency departm...

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Bibliographic Details
Published in:Clinical imaging 2022-04, Vol.84, p.31-35
Main Authors: Yang, Sara K., Zhang, Andrew, Hazany, Saman, Huang, Jimmy, Hathout, Gasser M.
Format: Article
Language:English
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Summary:Congenital aortic arch anomalies and variants have been extensively characterized in the medical literature. Proper identification of these anomalies is important when surgical or percutaneous interventions are indicated. We present a case of a 48-year old male who presented to the emergency department with altered mental status. Magnetic resonance angiography (MRA) findings revealed an aberrant right subclavian artery (ARSA), early bifurcation of the right common carotid artery (CCA) with anomalous origin of the right vertebral artery (VA) from the right common carotid artery bifurcation, anomalous left vertebral artery originating from the aortic arch, and absent left common carotid artery with independent origins of the left external carotid artery (ECA) and internal carotid artery (ICA). No other abnormalities were identified, and the patient demonstrated no symptoms attributable to his vascular anomalies. To our knowledge, this unique combination of anomalies has never been reported in the literature. With an understanding of embryological pathways, even exceedingly rare anomalies like this one can be explained. •Congenital aortic arch anomalies and variants are common findings on MRA neck examinations.•Proper identification is important for potential surgical and percutaneous interventions.•A review of embryology can help us to better understand the development of congenital arch anomalies and variants.•With an understanding of embryologic pathways, even exceedingly rare and complicated anomalies can be explained.
ISSN:0899-7071
1873-4499
DOI:10.1016/j.clinimag.2022.01.001