We present the case of a 15-year-old boy with
symptoms due to Klippel–Feil syndrome. Radiographs and CT scans demonstrated
basilar impression, occipitalisation of C1 and fusion of C2/C3.
MRI showed ventral compression of the medullocervical junction.
Skull traction was undertaken pre-operatively to determine whether
the basilar impression could be safely reduced. During traction,
the C3/C4 junction migrated 12 mm caudally and spasticity resolved.
Peri-operative skull-femoral traction enabled posterior occipitocervical
fixation without decompression. Following surgery, cervical alignment
was restored and spasticity remained absent. One year after surgery
he was not limited in his activities.
We present the case of an 83-year-old man who developed quadriparesis and respiratory embarrassment following osteomyelitis at the occipito-atlantoaxial junction. He had developed an abscess at this site after an earlier urinary infection with methicillin-resistant staphylococcus aureus. Stabilisation of the neck and antibiotic therapy led to an almost complete neurological recovery without recourse to anterior surgery.