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Recurrent posterior circulation infarction caused by anomalous occipital bony process in a young patient
© Song et al.; licensee BioMed Central. 2014
Received: 30 July 2014
Accepted: 11 December 2014
Published: 18 December 2014
Structural anomaly of the cervical spine or craniocervical junction has been reported as one of the rare causes of ischemic stroke. We report a case of a young patient with recurrent posterior circulation infarction that may have been associated with an anomalous occipital bony process compressing the vertebral artery.
A 23-year-old man experienced recurrent posterior circulation infarction 5 times over a period of 5 years. He had no conventional vascular risk factors. Young age stroke work-up including thorough cardiac, intra- and extracranial vascular evaluation and laboratory tests for the hypercoagulable state or connective tissue disease yielded unremarkable results. An anomalous bony process from the occipital base compressing the left vertebral artery was observed on brain CT. All the recurrent strokes were explainable by the arterial thromboembolism originating from the compressed left vertebral artery. Therefore, the left vertebral artery compressed by the anomalous occipital bony process may have been the culprit behind the recurrent thromboembolic strokes in our patient. Intractable recurrent strokes even under optimal medical treatment led us to make a decision for the intervention. Instead of surgical removal of the anomalous occipital bony process, the left vertebral artery was occluded permanently by endovascular coiling after confirming that this would cause no neurological deficits or flow disturbance in the posterior circulation. There was no recurrence of stroke for 2 years after permanent occlusion of the left vertebral artery.
Arterial thromboembolism originating from the left vertebral artery compressed by the anomalous occipital bony process is a rare but not to be overlooked cause of posterior circulation infarction. When intractable to medical treatment, endovascular occlusion of the vertebral artery without flow disturbance to the posterior circulation may be a useful treatment option when surgical removal is not feasible.
Cerebral infarction in young people is rare. Infarction at a young age may have distinct causes such as hypercoagulability, connective tissue disease, cerebral or cervical arterial dissection, or cardiac problems -. Particularly, recurrent cerebral infarction indicates a higher possibility of the presence of unusual underlying causes. Structural anomaly of the cervical spine or craniocervical junction has been reported as one such unusual cause of infarction ,. We report the case of a young patient with recurrent posterior circulation infarction that may have been associated with an anomalous occipital bony process compressing the vertebral artery.
A 23-year-old man had a history of recurrent cerebral infarction localized to the vascular territory of posterior circulation. He had no conventional vascular risk factors for stroke. Laboratory findings including lipid profile, D-dimer level, and autoimmune antibody tests were unremarkable. In addition, cardioembolism was excluded after a detailed cardiological evaluation including electrocardiography, echocardiography, 24-hr Holter monitoring, and cardiac CT.
Two months later, he experienced dizziness again (second stroke, September 2008). Brain MRI showed acute infarction in the left cerebellum and paramedian pons with thromboembolus at the distal basilar artery (Figure 1B). Then, cilostazol (200 mg) and warfarin were added to his regimen. One month later, warfarin was withdrawn for the concern of bleeding in long-term anticoagulation. However, triple antiplatelet therapy including aspirin, clopidogrel, and cilostazol was continued.
Nine months later, he experienced left arm weakness (third stroke, June 2009). Brain MRI revealed acute infarction in the right medial thalamus and paravermian cerebellum along with thromboembolus at the distal basilar artery (Figure 1C). Warfarin was added again to triple antiplatelet therapy. He recovered without neurological deficit. Ten months later, warfarin was withdrawn again for the concern of bleeding in long-term anticoagulation. Three years later, he experienced dysarthria and ataxia (fourth stroke, May 2012). Acute infarction was found in the vascular territory of the left posterior inferior cerebellar artery. CT angiography revealed thromboembolus at the distal basilar artery again (Figure 1D).
In the previous studies, the stroke mechanism of patients with infarction aged below 50 years was reported -. According to the Trial of Org 10172 in Acute Stroke Treatment (TOAST) classification of stroke mechanism, the proportion of other determined etiology in young–age stroke is rather high: large-artery atherosclerosis, 11%, cardioembolism, 24%, small-artery occlusion, 8%, stroke of other determined etiology, 27%, and stroke of undetermined etiology, 29% . Vertebral arterial injuries associated with structural osseous anomaly, one of other determined etiology, have been reported ,.
Anomalous occipital bony process may be a byproduct of fusion abnormalities -. The incidence of anomaly of atlanto-occipital fusion that could cause compression of the vertebral artery varies between 0.5% and 1.0% ,. The symptoms may be headache, neck pain, numbness, and weakness in the limbs, or cranial nerve dysfunction including tinnitus, visual disturbance, dysphagia, or dysarthria . The vertebral artery may be compressed mechanically during head rotation by adjacent bony structures and dynamic disturbance of blood flow can occur ,. Bow hunter’s syndrome is defined as symptomatic vertebrobasilar insufficiency caused by transient mechanical occlusion of the vertebral artery during head rotation . Meanwhile, vertebral artery injury attributable to the recurrent compression by the anomalous occipital bony process causing thrombosis may give rise to infarction . In our patient, the anomalous occipital bony process had been compressing the vertebral artery even in the neutral position and no significant flow disturbance was induced by head rotation. Therefore, the recurrent thromboembolism in our patient might have originated from the endothelial injury of the compressed vertebral artery rather than from direct mechanical compression by head rotation. The stroke mechanism in our patient may be different from that in typical bow hunter’s syndrome. A focal stenotic signal between the occipital bony process and vertebral arterial lumen may suggest the presence of endothelial or perivascular inflammatory tissue or the occurrence of subintimal dissection caused by repetitive mechanical compression. Therefore, we were concerned about the possibility that residual organized stenosis even after the surgical removal of the anomalous occipital bony process may work as a persistent embolic source. No further stroke after permanent occlusion of the left vertebral artery may provide evidence that recurrent arterial thromboembolism originating from the compressed left vertebral artery might be the cause of recurrent posterior circulation infarction in our patient.
After the second and third stroke, we added warfarin to the triple antiplatelet therapy. However, when warfarin was discontinued, the stroke recurred (third and fourth strokes). The fifth stroke occurred even under adequate anticoagulation and triple antiplatelet therapy. Therefore, we considered the following treatment options: 1) anticoagulation with higher international normalized ratio (INR 2.5-3.5) and triple antiplatelet therapy, 2) surgical resection of the anomalous occipital bony process, or 3) endovascular occlusion of the vertebral artery.
Life-long anticoagulation with higher INR and triple antiplatelet therapy in a young patient was considered risky owing to the possibility of bleeding complications in long-term treatment. Cases of young patients with recurrent posterior circulation infarction associated with the occipital bony process have been reported recently ,. The authors suggested that the bony protuberance possibly caused thrombi formation, and surgical removal was performed successfully as a permanent treatment ,. Considering the relatively smaller contralateral vertebral artery in our patient, surgical removal of the anomalous occipital bony process, saving both the vertebral arteries, might have been the best treatment option. However, in addition to the risk of surgical complications in cervical spine surgery (4-8%) ,, residual persistent organized stenosis of the vertebral artery even after the surgical removal of anomalous occipital bony process may work as a future recurrent embolic source. Hence, we chose endovascular treatment instead of surgical removal. Because the contralateral vertebral artery was smaller, the left vertebral artery was occluded after confirming the absence of neurological deficits or flow disturbance in the posterior circulation when it was temporarily occluded during the endovascular procedure (Figure 4). Although there was no recurrence of stroke until 2 years after the permanent occlusion of the left vertebral artery, the long-term outcomes need to be followed to confirm that this procedure is safe as a permanent treatment.
Arterial thromboembolism originating from the left vertebral artery compressed by the anomalous occipital bony process is a rare but not to be overlooked cause of posterior circulation infarction. When intractable to medical treatment, endovascular occlusion of the vertebral artery without flow disturbance of the posterior circulation may be a useful option when surgical removal is not feasible.
We obtained written informed consent from the patient for publication of this case report and any accompanying images.
- Dash D, Bhashin A, Pandit AK, Tripathi M, Bhatia R, Prasad K, Padma MV: Risk factors and etiologies of ischemic strokes in young patients: a tertiary hospital study in north India. J Stroke. 2014, 16: 173-177. 10.5853/jos.2014.16.3.173.View ArticlePubMedPubMed CentralGoogle Scholar
- Larrue V, Berhoune N, Massabuau P, Calviere L, Raposo N, Viguier A, Nasr N: Etiologic investigation of ischemic stroke in young adults. Neurology. 2011, 76: 1983-1988. 10.1212/WNL.0b013e31821e5517.View ArticlePubMedGoogle Scholar
- Renna R, Pilato F, Profice P, Della Marca G, Broccolini A, Morosetti R, Frisullo G, Rossi E, De Stefano V, Di Lazzaro V: Risk factor and etiology analysis of ischemic stroke in young adult patients. J Stroke Cerebrovasc Dis. 2014, 23: e221-e227. 10.1016/j.jstrokecerebrovasdis.2013.10.008.View ArticlePubMedGoogle Scholar
- Cronin CA, Aldrich EF, Kittner SJ: Occipital bone abnormality causing recurrent posterior circulation strokes. Stroke. 2011, 42: e370-e372. 10.1161/STROKEAHA.110.612176.View ArticlePubMedPubMed CentralGoogle Scholar
- Tominaga T, Takahashi T, Shimizu H, Yoshimoto T: Rotational vertebral artery occlusion from occipital bone anomaly: a rare cause of embolic stroke. Case report. J Neurosurg. 2002, 97: 1456-1459. 10.3171/jns.2002.97.6.1456.View ArticlePubMedGoogle Scholar
- Campos Dd, Silva THd, Ellwanger JH, Goerck ML, Kipper JF, Piazza JL, Kraether Neto L: Atlanto-occipital fusion and its neurological complications: a case report. J Morphol Sci, 29:111–113Google Scholar
- Kassim NM, Latiff AA, Das S, Ghafar NA, Suhaimi FH, Othman F, Hussan F, Sulaiman IM: Atlanto-occipital fusion: an osteological study with clinical implications. Bratisl Lek Listy, 111:562–565Google Scholar
- Malhotra V, Leeds NE: Case report 277. Occipitalization of the atlas with severe cord compression. Skeletal Radiol. 1984, 12: 55-58. 10.1007/BF00373178.View ArticlePubMedGoogle Scholar
- Grossmann RI, Davis KR: Positional occlusion of the vertebral artery: a rare cause of embolic stroke. Neuroradiology. 1982, 23: 227-230. 10.1007/BF00342548.View ArticlePubMedGoogle Scholar
- Hanakita J, Miyake H, Nagayasu S, Nishi S, Suzuki T: Angiographic examination and surgical treatment of bow hunter's stroke. Neurosurgery. 1988, 23: 228-232. 10.1227/00006123-198808000-00018.View ArticlePubMedGoogle Scholar
- Madawi AA, Casey AT, Solanki GA, Tuite G, Veres R, Crockard HA: Radiological and anatomical evaluation of the atlantoaxial transarticular screw fixation technique. J Neurosurg. 1997, 86: 961-968. 10.3171/jns.1997.86.6.0961.View ArticlePubMedGoogle Scholar
- Wright NM, Lauryssen C: Vertebral artery injury in C1-2 transarticular screw fixation: results of a survey of the AANS/CNS section on disorders of the spine and peripheral nerves. J Neurosurg. 1998, 88: 634-640. 10.3171/jns.1998.88.4.0634.View ArticlePubMedGoogle Scholar
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