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Published on: July 24, 2012
Cervical Instability and Quadriparesis Requiring Stabilization in Pediatric Patient Caused by a Mutation in COL2A1
Abhinav Pandey1, Alexandra Giantini-Larsen1, Jeffrey P Greenfield1
1Department of Neurological Surgery, Weill Cornell Medicine/New York Presbyterian Hospital, New York, New York, USA.
Insights
A pediatric patient experienced spinal cord injury due to a rare COL2A1 collagen disorder. Surgical decompression and fusion led to gradual strength recovery, highlighting the importance of genetic diagnosis in pediatric spinal trauma.
Area of Science:
- Pediatric Neurology
- Genetics
- Orthopedic Surgery
Background:
- A 3-year-old male presented with acute flaccid plegia and lower extremity weakness.
- Cervical spine imaging revealed cord edema and hemorrhage at C1-C2, with a nonossified mass causing spinal canal stenosis.
Abstract:
A 3-year-old male with no past medical history presented with flaccid plegia of his upper extremities and significant weakness in his lower extremities after wrestling with his brother. Cervical spine magnetic resonance imaging was consistent with cord edema and intraparenchymal hemorrhage at C1-C2. A nonossified tissue mass at the expected location of the upper dens created narrowing of the canal at the C1-2 level and mass effect on the cord. Head computed tomography showed periventricular leukomalacia. Initial findings favored dysplasia of the odontoid with associated soft tissue mass/pannus caused by a possible underlying genetic or metabolic bone dyscrasia. The patient underwent suboccipital craniotomy/C1 laminectomy and occiput to C4 fusion, for decompression and stabilization. Genetic testing showed a COL2A1 collagen disorder, with the child harboring a de novo mutation for c.3455 G>T (p.G1152V). The patient was discharged to inpatient acute rehabilitation, with gradual improvement in strength in all 4 extremities.
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