Pediatric basilar invagination: Unveiling a rare complication of inflammatory bowel disease unclassified
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Autor
Slivková, Pavla
Jevič, Filip
Schmidtová, Barbora
Datum vydání
2024Publikováno v
PM and RRočník / Číslo vydání
16 (7)ISBN / ISSN
ISSN: 1934-1482ISBN / ISSN
eISSN: 1934-1563Metadata
Zobrazit celý záznamKolekce
Tato publikace má vydavatelskou verzi s DOI 10.1002/pmrj.13203
Abstrakt
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.
Klíčová slova
atlantoaxial rotatory dislocation, AARD, basilar invagination, BI, inflammatory bowel disease unclassified, IBDU, Case report
Trvalý odkaz
https://hdl.handle.net/20.500.14178/2558Licence
Licence pro užití plného textu výsledku: Creative Commons Uveďte původ 4.0 International