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Occipitocondylar hyperplasia: an unusual craniovertebral junction anomaly causing myelopathy. Case report
Chima Ohaegbulam1, Eric J Woodard, Mark Proctor
1Department of Neurosurgery, Children's Hospital, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA. cohaegbulam@partners.org
Abstract:
The authors of this brief case report describe a previously unreported developmental variant of the craniovertebral junction. A 10-year-old girl who presented with cervical myelopathy was found to have cervicomedullary compression by hypertrophic occipital condyles. Decompression was achieved via a midline dorsal approach with no complications. The embryology of this area is briefly reviewed to attempt to explain the origin of this anomaly.
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