Journal article
Craniocervical junction fusions in patients with hindbrain herniation and syringohydromyelia
Journal of neurosurgery. Spine, Vol.9(1), pp.1-9
07/2008
DOI: 10.3171/SPI/2008/9/7/001
PMID: 18590404
Abstract
Patients with hindbrain herniation or the so-called Chiari malformation Type I (CM-I) and/or syringohydromyelia are treated with dorsal decompression alone; however, a small percentage of patients with other associated abnormalities require concomitant dorsal craniocervical junction (CCJ) fusion. The authors surveyed the indications for CCJ fusions in this population.
A retrospective review of University of Iowa medical records and radiographs obtained between 1996 and 2005 was performed. Inclusion criteria encompassed patients with diagnoses of CM-I and/or syringohydromyelia requiring dorsal CCJ fusions, and others with CCJ abnormalities who had CM-I and/or syringohydromyelia.
Two hundred thirty-four patients were identified, all of whom were symptomatic at presentation. Their ages ranged from 2.5 to 86 years; 33% of the patients were < 16 years of age. Patients were categorized as follows, with some being assigned to > 1 category: Group I, congenital or acquired CCJ abnormalities with reducible bone compression (25% of patients); Group II, previous anterior CCJ/upper brainstem decompression (44%); Group III, occipitocervical complex instability with CM-I and/or syringohydromyelia but without CCJ bone abnormalities requiring adjunctive posterior fossa decompression (26%); and Group IV, musculoligamentous instability, either from pathological states or from muscle dehiscence from repeated posterior fossa procedures (14%). Instrumentation was used in 96% of patients, with all 96% receiving semirigid fixation with titanium loop and sublaminar cables; all fusion constructs incorporated autologous bone. At last follow-up evaluation, fusion was radiographically complete in 97%, and symptom improvement was seen in 92%.
Dorsal CCJ fusions are required in patients with CM-I and/or syringohydromyelia who have concomitant CCJ abnormalities (Groups I and II). A definite group (CM-I and/or syringohydromyelia) without bone abnormality exists (Groups III and IV). This may be due to muscle weakness secondary to a high syrinx.
Details
- Title: Subtitle
- Craniocervical junction fusions in patients with hindbrain herniation and syringohydromyelia
- Creators
- Albert J Fenoy - Department of Neurosurgery, University of Iowa Hospitals and Clinics, Iowa City, Iowa, USAArnold H MenezesKathleen A Fenoy
- Resource Type
- Journal article
- Publication Details
- Journal of neurosurgery. Spine, Vol.9(1), pp.1-9
- DOI
- 10.3171/SPI/2008/9/7/001
- PMID
- 18590404
- NLM abbreviation
- J Neurosurg Spine
- ISSN
- 1547-5654
- eISSN
- 1547-5646
- Publisher
- American Association of Neurological Surgeons; United States
- Language
- English
- Date published
- 07/2008
- Academic Unit
- Stead Family Department of Pediatrics; Neurosurgery; Otolaryngology
- Record Identifier
- 9984040385402771
Metrics
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