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C2椎体后部结构先天性缺如伴寰枢椎脱位和基底凹陷:一例报告并文献复习

Congenital Absence of Posterior Elements of C2 Vertebra with Atlanto-Axial Dislocation and Basilar Invagination: A Case Report and Review of Literature.

作者信息

Srivastava Sudhir Kumar, Nemade Pradip Sharad, Aggarwal Rishi Anil, Bhoale Sunil Krishna

机构信息

Department of Orthopaedics, Seth G.S. Medical College and KEM Hospital, Maharashtra, India.

出版信息

Asian Spine J. 2016 Feb;10(1):170-5. doi: 10.4184/asj.2016.10.1.170. Epub 2016 Feb 16.

DOI:10.4184/asj.2016.10.1.170
PMID:26949474
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4764531/
Abstract

Developmental anomalies of the axis are commonly encountered, especially anomalies involving the odontoid process. Anomalies of the posterior elements are uncommon. We describe a unique case of agenesis of posterior elements of C2 with basilar invagination and atlanto-axial dislocation. An obese 8-year-old boy presented with symptoms of cervical myelopathy. Radiological workup revealed a craniovertebral junction anomaly with occipitalised atlas, absent posterior elements of axis, and hypertrophied C3 spinous process. Atlanto-axial instability and basilar invagination was present. Magnetic resonance angiography revealed hypoplastic left vertebral artery. Traction with cervical tongs failed to improve the alignment and symptoms. Anterior trans-oral release, followed by posterior decompression and custom-made instrumentation, was done. The patient recovered completely and was asymptomatic at the end of two years. X-ray and computed tomography scan demonstrated reduction of basilar invagination and maintenance of alignment. This is the first case to be reported of agenesis of posterior elements of axis associated with basilar invagination. One should look for this condition in patients with hypertrophied spinous process of C3. Utilization of hypoplastic pedicle of axis serves as an additional fixation point to increase the stability of the construct.

摘要

枢椎发育异常较为常见,尤其是涉及齿突的异常。后部结构异常则不常见。我们描述了一例独特的病例,即C2后部结构发育不全合并基底凹陷和寰枢椎脱位。一名8岁肥胖男孩出现颈髓病症状。影像学检查显示颅颈交界区异常,包括枕化寰椎、枢椎后部结构缺如以及C3棘突肥大。存在寰枢椎不稳和基底凹陷。磁共振血管造影显示左侧椎动脉发育不全。使用颈钳牵引未能改善对线情况及症状。遂进行了前路经口松解,随后进行后路减压及定制器械固定。患者完全康复,两年后无症状。X线和计算机断层扫描显示基底凹陷减轻且对线良好。这是首例报道的枢椎后部结构发育不全合并基底凹陷的病例。对于C3棘突肥大的患者应留意这种情况。利用发育不全的枢椎椎弓根作为额外的固定点可增加固定结构的稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aff1/4764531/4fa65157bbfb/asj-10-170-g007.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aff1/4764531/fa6868e581fd/asj-10-170-g002.jpg
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本文引用的文献

1
Embryology and bony malformations of the craniovertebral junction.颅颈交界区的胚胎学与骨畸形
Childs Nerv Syst. 2011 Apr;27(4):523-64. doi: 10.1007/s00381-010-1358-9. Epub 2010 Dec 31.
2
A cervical myelopathy caused by invaginated anomaly of laminae of the axis in spina bifida occulta with hypoplasia of the atlas: case report.隐性脊柱裂伴寰椎发育不全的枢椎板内陷性异常引起的颈髓病变:病例报告。
Spine (Phila Pa 1976). 2010 Apr 20;35(9):E351-5. doi: 10.1097/BRS.0b013e3181cb467c.
3
Cervical myelopathy associated with congenital C2/3 canal stenosis and deficiencies of the posterior arch of the atlas and laminae of the axis: case report and review of the literature.
颈椎管狭窄症伴先天性 C2/3 椎管狭窄和寰椎后弓及枢椎椎板缺如:病例报告及文献复习。
Spine (Phila Pa 1976). 2009 Nov 15;34(24):E886-91. doi: 10.1097/BRS.0b013e3181b64f0a.
4
Congenital osseous anomalies of the upper cervical spine.上颈椎先天性骨异常。
J Bone Joint Surg Am. 2008 Feb;90(2):337-48. doi: 10.2106/JBJS.G.00014.
5
Open reduction of irreducible atlantoaxial dislocation by transoral anterior atlantoaxial release and posterior internal fixation.经口前路寰枢椎松解及后路内固定治疗难复性寰枢椎脱位的切开复位术
Spine (Phila Pa 1976). 2006 May 15;31(11):E306-13. doi: 10.1097/01.brs.0000217686.80327.e4.
6
Embryology of the spine and associated congenital abnormalities.脊柱胚胎学及相关先天性异常
Spine J. 2005 Sep-Oct;5(5):564-76. doi: 10.1016/j.spinee.2004.10.044.
7
Atlantoaxial dislocation associated with the maldevelopment of the posterior neural arch of axis causing compressive myelopathy.寰枢椎脱位与枢椎后神经弓发育不良相关,导致压迫性脊髓病。
Neurol India. 2004 Dec;52(4):489-91.
8
C2 over C3 spondyloptosis in a case with absent posterior elements. Report of an unusual case and analysis of treatment options.一例后结构缺如患者的C2椎体相对于C3椎体发生脊柱滑脱。罕见病例报告及治疗方案分析。
J Clin Neurosci. 2004 Aug;11(6):675-7. doi: 10.1016/j.jocn.2003.01.003.
9
Congenital absence of the posterior elements of C2 vertebra: a case report.先天性C2椎体后部结构缺失:一例报告
Neurol India. 2003 Jun;51(2):250-1.
10
Congenital osseous anomalies of the upper and lower cervical spine in children.儿童上下颈椎的先天性骨异常
J Bone Joint Surg Am. 2002 Feb;84(2):277-88. doi: 10.2106/00004623-200202000-00017.