A lthough anomalies of the upper cervical spine are not uncommon and have multiple variations, 7 only 5 cases of cervical myelopathy caused by invagination of an anomalous lamina of the axis have been reported. [1][2][3][4][5] We describe an extremely rare case of cervical myelopathy caused by invagination of the bilaterally separated lamina of the axis and present a review of the literature.
Case ReportThe patient was informed that the authors would describe his case for publication and he provided consent.
History.A previously healthy 68-year-old man reported bilateral hand numbness that began 1 year before admission to Kansai Rosai Hospital in Amagasaki, Japan. During the year before admission, he had also experienced a slowly progressive gait disturbance, clumsiness of his right hand, and right dominant sensory disturbance in all 4 extremities and the trunk. He had no history of neck or head injury.Examination. Physical examination at admission revealed right dominant hypesthesia of all 4 extremities and the trunk, motor weakness of the right hand, and diffuse hyperreflexia in all extremities.A lateral radiograph of the cervical spine showed a bony abnormality in the spinal canal at the C-2 level (Fig. 1). No instability was evident on lateral flexion/extension radiographs. Magnetic resonance images taken before surgery showed that the spinal cord was markedly comCervical myelopathy caused by invagination of anomalous lamina of the axis
Department of Orthopaedic Surgery, Kansai Rosai Hospital, Amagasaki, JapanThe authors report a case of cervical myelopathy caused by invagination of the bilaterally separated lamina of the axis. They also present a literature review.The patient was a previously healthy 68-year-old man with a 1-year history of slowly progressive gait disturbance, right-hand clumsiness, and right dominant sensory disturbance in his trunk and extremities. Both MRI and CT showed that the spinal cord was markedly compressed at the C2-3 level, on the right side, by a deeply invaginated anomalous lamina of the axis. A bilaterally separated lamina was also visible. The patient underwent removal of the anomalous invaginated fragment of the separated lamina and the spinous process of the axis. One year after surgery, his myelopathic symptoms had almost completely resolved.Here, the authors present the case of a patient with an extremely rare anomaly of the lamina of the axis. The underlying pathogenesis of this anomaly could be the failure of the 2 chondrification centers on either side to fuse into a single ossification center. Surgical removal of the anomalous invaginated lamina produced a satisfactory outcome.