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Left-sided cervical aortic arch associated with pseudocoarctation, aneurysm formation, and anomalous left
Nabil J Khoury1, Roula Hourani, Ghina A Birjawi
1Department of Diagnostic Radiology, American University of Beirut Medical Center, Beirut, Lebanon.
Insights
Cervical aortic arch (CAA), a rare congenital anomaly, can present with aneurysm and pseudocoarctation. This case report details an extremely rare combination of CAA with these conditions and a novel associated venous anomaly.
Area of Science:
- Cardiovascular Medicine
- Medical Imaging
- Congenital Anomalies
Background:
- Cervical aortic arch (CAA) is a rare congenital anomaly of the aorta.
- CAA can be associated with various cardiovascular abnormalities, including aortic aneurysms and pseudocoarctation.
- The combined occurrence of CAA with both aneurysm and pseudocoarctation is exceptionally rare.
Observation:
- This report presents a unique case of cervical aortic arch (CAA).
- The patient exhibited a rare combination of aortic aneurysm and pseudocoarctation.
- An anomalous subaortic left brachiocephalic vein, not previously linked to CAA, was also identified.
Findings:
- Multidetector computed tomography (MDCT) and magnetic resonance angiography (MRA) were used for imaging.
- Radiographic findings confirmed the cervical aortic arch, aneurysm, and pseudocoarctation.
- The anomalous venous structure was visualized and documented.
Implications:
- This case expands the spectrum of known cardiovascular abnormalities associated with CAA.
- The findings highlight the importance of comprehensive imaging in diagnosing complex congenital aortic anomalies.
- The description of a novel venous anomaly associated with CAA may prompt further research into embryological development and clinical correlations.
Abstract:
Cervical aortic arch (CAA) is a rare congenital aortic anomaly. It can be associated with several cardiovascular abnormalities including aortic aneurysm, valvular disease, and pseudocoarctation. In this report, we present a case of CAA with combined association of both aneurysm formation and pseudocoarctation. This combination of anomalies is extremely uncommon, described in only 4 cases in the literature. In addition, our patient had an anomalous subaortic left brachiocephalic vein that, to our knowledge, was not previously described in the literature to be associated with CAA. The radiographic, multidetector computed tomography scan, and magnetic resonance angiography imaging findings are presented.
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