Srivastava Sudhir Kumar, Nemade Pradip Sharad, Aggarwal Rishi Anil, Bhoale Sunil Krishna
Department of Orthopaedics, Seth G.S. Medical College and KEM Hospital, Maharashtra, India.
Asian Spine J. 2016 Feb;10(1):170-5. doi: 10.4184/asj.2016.10.1.170. Epub 2016 Feb 16.
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.
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。