Abstract
Keywords
Vertebral Artery Duplication Multidetector Computed Tomography Magnetic Resonance Angiography
1. Introduction
The vertebral arteries (VAs) are among the major arteries of the neck. They supply blood to the upper spinal cord, brainstem, cerebellum, and posterior part of brain as the vertebrobasillar system. Anatomically, they usually arise from the first part of the subclavian arteries. There are variable developmental variations in the origin of the VA; these variations are associated with diverse clinical manifestations. Duplication of the VA is very rare; its incidence was only 0.164% in a recent large-scale study involving the Chinese population (1). This variant shows a dual origin of VA with fusion at variable levels in the neck (2). This condition can be misdiagnosed as a dissection of the VA, arterial hypoplasia, or arterial narrowing on selective catheter angiography (3, 4). A complete understanding of the variations in vertebral arteries is important for performing angiography or vascular interventional surgery. In this study, we present a case of left VA duplication in a patient who presented with dizziness. The left VA duplication was detected on both magnetic resonance angiography (MRA) and computed tomography angiography (CTA) examinations. We have also reviewed the embryological significance of and previous literature regarding this condition.
A 52-year-old woman with left duplicated vertebral artery. A, Three dimensional time-of-flight magnetic resonance angiography (3D TOF MRA) of right oblique view shows the double origin (arrows) of the left vertebral artery. Two limbs of the left' vertebral artery (VA) fused to form the distal part of the left VA (arrowhead). B, Contrast-enhanced computed tomography angiography (CTA) maximum intensity projection image demonstrated the dual origin of the left vertebral artery. The medial limb originated from the left aortic arch (black arrow) and lateral limb originated from the left subclavian artery (white arrow). The two limbs united to form one main trunk (arrow head). C, Axial source image of CTA demonstrated a medial limb (arrow) originated from the aortic arch and a lateral limb (arrowhead) originated from the left subclavian artery at the C6 vertebra level.
Cases of Duplicated Origin of the Vertebral Artery Proved by Imaging Modality Since 2000
| Author, Y/ref | Age | Sex | Laterality | Level of Union | Imaging Modality | Symptom | Disease or Clinical Status |
|---|---|---|---|---|---|---|---|
| Goddard et al. (2001) (2) | 66 | F | Right | Level of carotid bifurcation | MRA, DSA | Dysarthria, hemisensory disturbance, hemiplegia | Cerebral infarction |
| 49 | M | Right | Level of carotid bifurcation | MRA | None | ICA occlusion | |
| Ionete C. et al. (2006) (5) | 83 | M | Bilateral | Right: C4 - 5, Left: C5 - 6 | MRA | Cognitive impairment | None |
| Satti SR. et al. (2007) (11) | 53 | F | Right | C3 | DSA | Headache | Aneurysm |
| 62 | M | Left | C7 | DSA | Presyncope | None | |
| Thomas et al. (2008) (3) | 49 | F | Right | C6 | DSA | None | Aneurysm |
| Harnier et al. (2008) (12) | 61 | F | Right | Not mentioned | MRA | Dizziness | None |
| Mordasini P. et al. (2008) (13) | 48 | M | Bilateral | Bilateral, C4 - 5 | MRA | Not mentioned | Cerebral infarction |
| Kim DW et al. (2009) (14) | 42 | F | Left | C5 | DSA | Weakness , hemisensory disturbance | AVF |
| Kendi ATK et al. (2009) (6) | 59 | F | Left | C5 - 6 | CTA | Headache | Aneurysm |
| Meila et al. (2012) (8) | 54 | F | Right | C4 | CTA | Not mentioned | None |
| 43 | F | Bilateral | C4 | CTA | Severe headache | Subarachnoid hemorrhage | |
| 56 | F | Left | C5 | CTA | Not mentioned | Aneurysm | |
| Melki et al. (2012) (15) | 51 | M | Right | C5 - 6 | CTA, MRA | Acute vertigo | Cerebellar infarction |
| Polguj et al. (2013) (7) | 43 | M | Left | C5 - 6 | CTA | Headache, left limb weakness | Right ICA dissection |
| Shin SW et al. (2013) (16) | 51 | F | Left | C4 | CTA, MRA, DSA | None | Aneurysm |
| Rameshbabu et al. (2014) (9) | 36 | M | Right | C4 - 5 | CTA | Dizziness | None |
| Baik JY et al. (2016) (17) | 69 | F | Right | Not mentioned | MRA | Headache | None |
| Jung SG et al. (2016) (18) | 63 | F | Left | C4 | DSA | Vertigo | Cerebellar infarction |
| Our case | 52 | F | Left | C5 - 6 | CTA, MRA | Headache, dizziness | None |
2. Case Presentation
A 52-year-old woman presented with a two-week history of headache and dizziness. The patient showed no other clinical abnormality or significant past medical history. She underwent brain magnetic resonance imaging (MRI) with 3D time-of-flight (TOF) intracranial MRA and gadolinium-enhanced neck MRA using a 1.5-Tesla system (Intera, Philips Medical Systems, Best, The Netherlands) and contrast enhanced computed tomography angiography (CTA) of the neck using a 128-slice CT scanner (SOMATOM Definition AS+, Siemens Healthcare, Forchheim, Germany). No abnormal focal lesion in the brain parenchyma was observed on routine brain MRI. Intracranial vessels observed on 3D TOF MRA were also normal. The dual origin of the left VA was noted on contrast enhanced MRA and CTA of the neck were demonstrated a dual origin of the left vertebral artery (Figure 1). The medial limb and lateral limb of the left VA were noted to originate from the left aortic arch and left subclavian artery, respectively. After their origins, the medial limb looped slightly forwards and ascended behind the left common carotid artery, while the lateral limb looped slightly poster laterally and ascended behind the medial limb. They united to form a single main trunk at the level of the C5 - 6 disk (about 5.6 cm from the medial orifice and 3.4 cm from the lateral orifice). The diameters of the medial and lateral limbs at the points of origin were 2.3 mm and 2.0 mm, respectively. The diameter of the distal common trunk of the left VA was 3.0 mm at the anastomosis of the two limbs (C5-6 disk level). The diameter of the right VA at the same level (C5 - 6 disk level) was 3.4 mm. The patient’s symptoms were relieved following conservative management.
3. Discussion
Fenestration and duplication of the vertebral arteries are considered as developmental anomalies (5). The term “fenestration” refers to two parallel segments of the VA with a single origin, while the term “duplication” refers to a VA that has two origins with fusion at various levels in the neck (5, 6).
Embryologically, the VAs typically originate from the distal ends of the seventh dorsal intersegmental arteries. The longitudinal anastomoses between the cervical intersegmental arteries form the VAs. The intersegmental arteries eventually regress, except the seventh, which becomes the proximal subclavian artery (SCA) containing the origin of the VA. Persistence of the intersegmental artery and abnormal development of the aortic arch can cause duplication of the VA (7). Persistence of the right fourth or fifth intersegmental arteries leads to a dual origin of the VA from the SCA or brachiocephalic trunk on the right side, or an aortic or a dual origin of the VA on the left side (4). The level of entrance into the transverse foramen indicates the intersegmental artery that persists (8).
Duplicated VAs are rarely reported in the literature. Komiyama et al. reviewed 26 cases of duplicated VAs reported before 1999 (4). Since 2000, we found 20 additional cases (including our case) of duplicated VAs confirmed by an imaging modality (Table 1). Overall, 22 cases had a left duplicated VA and 21 cases had a right duplicated VA. Three patients had duplicated VA on both sides. In most cases, the medial limb originated from the aorta and the lateral limb originated from the subclavian artery. Either limb of the duplicated artery may also arise from the common carotid artery, brachiocephalic trunk, or thyrocervical trunk (4, 9). The fusion levels varied from C3 to C7 (Table 1).
The clinical presentation of duplicated VA is nonspecific; most of the reported cases are incidental findings in autopsy series, angiography, or MRA studies (1, 2, 5). However, anecdotal reports suggest that this vascular anomaly may be a predisposing factor to VA dissection, intracranial aneurysm, kinking, and arteriovenous malformation (9). Whether the duplicated VA is associated with other pathologic conditions is still matter of debate.
Recognizing duplication of the VA is important in several clinical situations. First, a duplicated VA can mimic a VA dissection when a filling defect is created at the union of the two limbs, due to the mixing of contrast-containing blood from one limb and non-contrast- containing blood from the other limb during angiography (10). Second, an abrupt change in the diameter of the duplicated VA may occur at the level of the anastomosis. This might be confused with hypoplasia or pathologic narrowing of the vessel. In addition, the smaller lumen of the duplicated VA can influence the selection of the route for endovascular treatment (3, 5).
Complete knowledge of the vessel anatomy and variations is important during diagnostic and interventional angiography, to prevent unintentional diagnostic or therapeutic challenges. This report can be helpful in identifying unexpected vascular variations on CTA or MRA and differentiate this anatomical variation from other pathologic conditions in clinical practice such as dissection, arterial hypoplasia, or arterial narrowing.
Acknowledgements
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