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表现为对侧展神经麻痹的椎动脉夹层动脉瘤

Dissecting aneurysm of vertebral artery manifestating as contralateral abducens nerve palsy.

作者信息

Jeon Jin Sue, Lee Sang Hyung, Son Young-Je, Chung Young Seob

机构信息

Department of Neurosurgery, Seoul National University Hospital, Seoul, Korea.

出版信息

J Korean Neurosurg Soc. 2013 Mar;53(3):194-6. doi: 10.3340/jkns.2013.53.3.194. Epub 2013 Mar 31.

DOI:10.3340/jkns.2013.53.3.194
PMID:23634273
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3638276/
Abstract

Isolated abducens nerve paresis related to ruptured vertebral artery (VA) aneurysm is rare. It usually occurs bilaterally or ipsilaterally to the pathologic lesions. We report the case of a contralateral sixth nerve palsy following ruptured dissecting VA aneurysm. A 38-year-old man was admitted for the evaluation of a 6-day history of headache. Abnormalities were not seen on initial computed tomography (CT). On admission, the patient was alert and no signs reflecting neurologic deficits were noted. Time of flight magnetic resonance angiography revealed a fusiform dilatation of the right VA involving origin of the posterior inferior cerebellar artery. The patient suddenly suffered from severe headache with diplopia the day before the scheduled cerebral angiography. Neurologic examination disclosed nuchal rigidity and isolated left abducens nerve palsy. Emergent CT scan showed high density in the basal and prepontine cistern compatible with ruptured aneurismal hemorrhage. Right vertebral angiography illustrated a right VA dissecting aneurysm with prominent displaced vertebrobasilar artery to inferiorly on left side. Double-stent placement was conducted for the treatment of ruptured dissecting VA aneurysm. No diffusion restriction signals were observed in follow-up magnetic resonance imaging of the brain stem. Eleven weeks later, full recovery of left sixth nerve palsy was documented photographically. In conclusion, isolated contralateral abducens nerve palsy associated with ruptured VA aneurysm may develop due to direct nerve compression by displaced verterobasilar artery triggered by primary thick clot in the prepontine cistern.

摘要

孤立性外展神经麻痹与椎动脉(VA)动脉瘤破裂相关的情况较为罕见。它通常双侧或与病损同侧发生。我们报告一例椎动脉夹层动脉瘤破裂后出现对侧第六神经麻痹的病例。一名38岁男性因头痛6天入院评估。初次计算机断层扫描(CT)未见异常。入院时,患者神志清醒,未发现神经系统缺损体征。时间飞跃磁共振血管造影显示右侧椎动脉梭形扩张,累及小脑后下动脉起源处。在预定的脑血管造影前一天,患者突然出现严重头痛伴复视。神经系统检查发现颈项强直和孤立性左侧外展神经麻痹。急诊CT扫描显示基底池和脑桥前池高密度影,符合动脉瘤破裂出血。右侧椎动脉血管造影显示右侧椎动脉夹层动脉瘤,椎基底动脉明显向左下移位。对破裂的椎动脉夹层动脉瘤进行了双支架置入治疗。脑干的随访磁共振成像未观察到弥散受限信号。11周后,左侧第六神经麻痹完全恢复,有照片记录为证。总之,与椎动脉动脉瘤破裂相关的孤立性对侧外展神经麻痹可能是由于脑桥前池原发性厚血凝块引发的椎基底动脉移位直接压迫神经所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3638276/fe16e81ea837/jkns-53-194-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3638276/49990b105821/jkns-53-194-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3638276/319756481751/jkns-53-194-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3638276/fe16e81ea837/jkns-53-194-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3638276/49990b105821/jkns-53-194-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3638276/319756481751/jkns-53-194-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3638276/fe16e81ea837/jkns-53-194-g003.jpg

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