Pediatric basilar invagination: Unveiling a rare complication of inflammatory bowel disease unclassified
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Author
Slivková, Pavla
Jevič, Filip
Schmidtová, Barbora
Publication date
2024Published in
PM and RVolume / Issue
16 (7)ISBN / ISSN
ISSN: 1934-1482ISBN / ISSN
eISSN: 1934-1563Metadata
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This publication has a published version with DOI 10.1002/pmrj.13203
Abstract
This case report details the presentation of an 8-year-old boy with atlantoaxial rotatory dislocation (AARD) and basilar invagination (BI), an exceedingly rare complication of inflammatory bowel disease unclassified (IBDU). Basilar invagination, an anomaly of the craniovertebral junction, results in the odontoid protruding into the foramen magnum. It may be associated with concurrent abnormalities such as atlantoaxial dislocation, Chiari malformation, atlas occipitalization, Klippel-Feil syndrome, atlanto-occipital hypoplasia, among others. To the best of our knowledge, this represents the first documented case reporting basilar invagination as a life-threatening complication of inflammatory bowel disease (IBD) in children.
Keywords
atlantoaxial rotatory dislocation, AARD, basilar invagination, BI, inflammatory bowel disease unclassified, IBDU, Case report
Permanent link
https://hdl.handle.net/20.500.14178/2558License
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