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本文引用的文献

1
Operative nuances to safeguard anomalous vertebral artery without compromising the surgery for congenital atlantoaxial dislocation: untying a tough knot between vessel and bone.保障椎动脉异常而不影响先天性寰枢椎脱位手术的手术要点:解开血管与骨骼之间的棘手结。
J Neurosurg Spine. 2014 Jan;20(1):5-10. doi: 10.3171/2013.9.SPINE13491. Epub 2013 Nov 1.
2
Klippel-Feil syndrome with atlanto-axial dislocation, anomalous vertebral artery, dextrocardia and situs inversus.伴有寰枢椎脱位、椎动脉异常、右位心和内脏反位的克-费综合征。
Clin Neurol Neurosurg. 2013 Oct;115(10):2304-6. doi: 10.1016/j.clineuro.2013.08.011. Epub 2013 Aug 16.
3
Anomalous vertebral arteries in the extra- and intraosseous regions of the craniovertebral junction visualized by 3-dimensional computed tomographic angiography: analysis of 100 consecutive surgical cases and review of the literature.颅颈交界区硬骨内外异常椎动脉的三维 CT 血管造影表现:100 例连续手术病例分析及文献复习。
Spine (Phila Pa 1976). 2012 Oct 15;37(22):E1389-97. doi: 10.1097/BRS.0b013e31826a0c9f.
4
Congenital atlantoaxial dislocation: a dynamic process and role of facets in irreducibility.先天性寰枢关节脱位:一个动态过程和小关节面在难复性中的作用。
J Neurosurg Spine. 2011 Dec;15(6):678-85. doi: 10.3171/2011.7.SPINE1152. Epub 2011 Aug 19.
5
"Stretched loop sign" of the vertebral artery: a predictor of vertebrobasilar insufficiency in atlantoaxial dislocation.椎动脉“拉伸环征”:寰枢椎脱位中椎基底动脉供血不足的一个预测指标。
Surg Neurol. 2006 Sep;66(3):298-304; discussion 304. doi: 10.1016/j.surneu.2006.02.032.
6
Morphogenesis of the posterior inferior cerebellar artery with three-dimensional reconstruction of the late embryonic vertebrobasilar system.胚胎晚期椎基底动脉系统三维重建下小脑后下动脉的形态发生
Surg Radiol Anat. 2005 Mar;27(1):56-60. doi: 10.1007/s00276-004-0303-6. Epub 2005 Jan 12.
7
Vertebral artery in relationship to C1-C2 vertebrae: an anatomical study.椎动脉与C1-C2椎体的关系:一项解剖学研究。
Neurol India. 2004 Jun;52(2):178-84.
8
A vertebral artery tortuous course below the posterior arch of the atlas (without passing through the transverse foramen). Anatomical report and clinical significance.寰椎后弓下方椎动脉走行迂曲(未通过横突孔)。解剖学报告及临床意义。
J Neurosurg Sci. 2003 Dec;47(4):183-7.
9
Subclavian artery supply disruption sequence: hypothesis of a vascular etiology for Poland, Klippel-Feil, and Möbius anomalies.锁骨下动脉供血中断序列:关于波兰综合征、克利佩尔-费尔综合征和莫比乌斯畸形血管病因的假说
Am J Med Genet. 1986 Apr;23(4):903-18. doi: 10.1002/ajmg.1320230405.

先天性不可复位寰枢椎脱位病例中的冗余异常椎动脉:强调与第一节间动脉的差异以及在进行C1-2关节操作时预防损伤的手术步骤。

Redundant anomalous vertebral artery in a case of congenital irreducible atlantoaxial dislocation: Emphasizing on the differences from the first intersegemental artery and operative steps to prevent injury while performing C1-2 joint manipulation.

作者信息

Patra Devi P, Salunke Pravin S, Sahoo Sushanta K, Ghuman Mandeep S

机构信息

Department of Neurosurgery.

Radiodiagnosis PGIMER, Chandigarh, INDIA.

出版信息

Ann Neurosci. 2015 Oct;22(4):245-7. doi: 10.5214/ans.0972.7531.220412.

DOI:10.5214/ans.0972.7531.220412
PMID:26527042
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4627206/
Abstract

Anomalous vertebral artery (VA), commonly the persistent first intersegmental artery (FIA) is often seen with congenital atlantoaxial dislocations (AAD). An unusual redundant/ectatic loop of VA passing below the C1 (upside down VA) has been described below and appears to be different from FIA. The operative technique to protect it while C1-2 joint manipulation has been described. A 35 year old male presented with progressive spastic quadriparesis after trivial trauma. Radiology showed irreducible atlantoaxial dislocation with occipitalised C1 and C2-3 fusion. The left VA was anomalous passing beneath the C1 arch with a redundant loop lying posterior to the C1-2 joint. This was unlike the persistent first intersegmental artery (FIA) and was safeguarded while dissecting the C1-2 facet. The artery was dissected and safeguarded while performing C1-2 joint manipulation. A redundant/ectatic loop lying posterior to C1-2 joint is an unusual variant of anomalous VA. Evaluation of preoperative radiology helps in diagnosing such anomalous VA. Dissection of the entire redundant loop of the anomalous artery is important in opening the C1-2 joint required for reduction and placement of spacer/ bone grafts to achieve good bony fusion. Also mobilizing the loop allows safe insertion of lateral mass screw. Care needs to be taken while fastening screws to prevent compression of the loop.

摘要

椎动脉异常(VA),通常为持续存在的第一节间动脉(FIA),常与先天性寰枢椎脱位(AAD)相关。一种不常见的椎动脉冗余/扩张袢从C1下方通过(椎动脉倒置)已在下文描述,且似乎与FIA不同。已描述了在C1 - 2关节操作时保护该异常椎动脉的手术技术。一名35岁男性在轻微外伤后出现进行性痉挛性四肢瘫。影像学检查显示不可复位的寰枢椎脱位,伴有枕化的C1和C2 - 3融合。左侧椎动脉异常,从C1弓下方通过,在C1 - 2关节后方有一个冗余袢。这与持续存在的第一节间动脉(FIA)不同,在解剖C1 - 2小关节时对其进行了保护。在进行C1 - 2关节操作时对该动脉进行了解剖和保护。位于C1 - 2关节后方的冗余/扩张袢是椎动脉异常的一种不常见变异。术前影像学评估有助于诊断此类椎动脉异常。解剖异常动脉的整个冗余袢对于打开C1 - 2关节以进行复位和置入间隔物/骨移植以实现良好的骨融合很重要。此外,移动该袢可安全置入侧块螺钉。在拧紧螺钉时需小心,以防止压迫该袢。