Hypoplasia of C1’s posterior arch: Is there an ideal anatomical classification?

Author:

Junior Messias Gonçalves Pacheco1,dos Santos Nicoly Augusta da Silva Quezada1,Ribeiro Raphael Tavares1,Landeiro Jose Alberto1,Pessoa Bruno Lima1

Affiliation:

1. Department of Neurosurgery, Antônio Pedro University Hospital, Federal Fluminense University, Niteroi, Rio de Janeiro, Brazil.

Abstract

Background: Congenital anomalies of the atlas are rare and usually occur in conjunction with other congenital variants. They include a wide spectrum of anomalies ranging from clefts to hypoplasia or aplasia of its arches that may contribute to spinal cord compressive syndrome. Case Description: A 54-year-old male presented with the sudden onset of a severe quadriparesis and loss of proprioception after a minor fall. The magnetic resonance (MR) scan showed cord compression at the C1 level attributed to C1 arch hypoplasia. Two months following a decompressive C1 laminectomy without fusion, and the patient was symptom free. Conclusion: Posterior C1 arch hypoplasia is a rare anomaly that can contribute to cervical cord compression and myelopathy. The optimal surgical management may include, as in this case, a posterior decompression without fusion.

Publisher

Scientific Scholar

Subject

Neurology (clinical),Surgery

Reference10 articles.

1. Spinal canal stenosis at the level of Atlas;Bhattacharjee;J Craniovertebr Junction Spine,2011

2. Congenital defects of the posterior arch of the atlas: A report of seven cases including an affected mother and son;Currarino;AJNR Am J Neuroradiol,1994

3. Congenital C1 arch deficiency: Grand round presentation;Elmalky;Eur Spine J,2013

4. Cervical spinal stenosis and myelopathy due to atlas hypoplasia;Hsu;J Chin Med Assoc,2007

5. Atlantal stenosis: A rare cause of quadriparesis in a child;Liliang;J Neurosurg,2000

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