Introduction: Chiari I malformation (CIM) is a congenital abnormality defined as downward
herniation of the cerebellar tonsils through the foramen magnum. Syringomyelia is present in
30–85% of cases. Magnetic resonance (MR) imaging has increased the frequency of
diagnosis of this complex disorder. Great variety exists in the indications and techniques
recommended for the surgical management of this complex. Methods: In a group of 23
prospectively selected patients (15 males and 8 females) having (CIM) with and without
syringomyelia (11 patients and 12 patients respectively) during a five years period from
January, 2005 to January, 2010. Cranio-cervical bony decompression alone was done in 8
patients, Cranio-cervical bony decompression with duroplasty was done in 12 patients, and
Cranio-cervical bony decompression with syringo-subarachnoid shunt was done in three
patients. Outcome was defined as good, fair, or bad. Results: During a mean follow-up
period of 32 months, the overall outcome was good in 19 patients (83%), fair in 3 patients
(13%), and bad in one patient (4%). No operative mortality or permanent post operative
morbidity was encountered. Transient post operative morbidity was encountered in 6 patients
(26%) namely mild temporary neurological deterioration, CSF leak, and mild wound sepsis.
There were no statistically significant differences between the various decompressive
approaches. Conclusion: Decompression of the cranio-cervical junction through suboccipital
craniectomy (SOC) with cervical laminectomy, duroplasty, or syringo-subarachnoid shunt is
the recommended surgical management option for CIM±S. Further studies utilizing larger
patient volumes are necessary to confirm our recommendation.
Research Department	
              
          Research Journal	
              Egyptian journal of neurological surgery 
          Research Member	
          
      Research Publisher	
              Egyptian society of neurological surgery
          Research Rank	
              2
          Research Vol	
              Vol25.no2 
          Research Website	
              NULL
          Research Year	
              2010
          Research_Pages	
              10
          Research Abstract	
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