Ahmet Taha Demirbas1,2, Ismet Demirtas3, Feyza Sonmez Topcu4, Sevilay Karasu3, Behcet Ayyıldiz3. 1. Clinical Anatomy PhD Program, Graduate School of Health Sciences, Istanbul Medipol University, Göztepe Neighborhood, Atatürk Street No:19, Beykoz, Istanbul, Turkey. tahademirbas@gmail.com. 2. Department of Anatomy, School of Medicine, Istinye University, Istanbul, Turkey. tahademirbas@gmail.com. 3. Department of Anatomy, School of Medicine, Istinye University, Istanbul, Turkey. 4. Department of Radiology, School of Medicine, Istinye University Liv Hospital, Istanbul, Turkey.
Abstract
BACKGROUND: Variations of the origin of the occipital artery (OA) can be considered as congenital anomalies that are often asymptomatic and detected incidentally on angiography or during cadaver dissection. While OA normally originates from the posterior aspect of the external carotid artery (ECA), recent evidence also reflects that OA may infrequently originate from the internal carotid artery (ICA); however, OA originating from the vertebral artery (VA) is a highly rare phenomenon. CASE PRESENTATION: In a 54-year-old female patient with the complaint of left hemiparesis, computed tomography (CT) angiography revealed nonstenotic calcified plaques at the beginning of right ICA where common carotid artery (CCA) bifurcates. We also incidentally observed that bilateral OA originated from the VA using maximum intensity projection (MIP) technique. In addition to this rare variation, CT angiography showed the osseous anomaly termed as high-riding VA (HRVA) in the C1/2 vertebral space of the V3 segment of the VA. CONCLUSION: To the best of our knowledge, a case of bilateral OA originating from the VA has not been reported to date. We believe that recognition of this rare variation may contribute to the relevant literature and it is of importance to consider this variation in radiological imaging and surgical procedures involving this region.
BACKGROUND: Variations of the origin of the occipital artery (OA) can be considered as congenital anomalies that are often asymptomatic and detected incidentally on angiography or during cadaver dissection. While OA normally originates from the posterior aspect of the external carotid artery (ECA), recent evidence also reflects that OA may infrequently originate from the internal carotid artery (ICA); however, OA originating from the vertebral artery (VA) is a highly rare phenomenon. CASE PRESENTATION: In a 54-year-old female patient with the complaint of left hemiparesis, computed tomography (CT) angiography revealed nonstenotic calcified plaques at the beginning of right ICA where common carotid artery (CCA) bifurcates. We also incidentally observed that bilateral OA originated from the VA using maximum intensity projection (MIP) technique. In addition to this rare variation, CT angiography showed the osseous anomaly termed as high-riding VA (HRVA) in the C1/2 vertebral space of the V3 segment of the VA. CONCLUSION: To the best of our knowledge, a case of bilateral OA originating from the VA has not been reported to date. We believe that recognition of this rare variation may contribute to the relevant literature and it is of importance to consider this variation in radiological imaging and surgical procedures involving this region.