Cervical myelopathy in hereditary multiple exostoses.

Détails

ID Serval
serval:BIB_3BB9DE876988
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Etude de cas (case report): rapporte une observation et la commente brièvement.
Collection
Publications
Institution
Titre
Cervical myelopathy in hereditary multiple exostoses.
Périodique
Joint, Bone, Spine
Auteur⸱e⸱s
Burki V., So A., Aubry-Rozier B.
ISSN
1778-7254 (Electronic)
ISSN-L
1297-319X
Statut éditorial
Publié
Date de publication
2011
Volume
78
Numéro
4
Pages
412-414
Langue
anglais
Notes
Publication types: Journal Article Publication Status: ppublish
Résumé
Spinal cord compression due to cervical exostoses is a rare but recognized complication of hereditary multiple exostosis (HME), an autosomal dominant disorder. This disease, also called multiple osteochondromatosis, is characterised by osteocartilaginous exostoses, typically involving the juxtaepiphyseal regions of long bones. Complications such as transformation to sarcoma (1 to 5%) or neurological compression (of the spinal cord, 1 to 9%) can arise during the course of the disease. We report the case of a 64-year-old man with progressive difficulties in walking over many years, ascribed to congenital rachitism. A diagnosis of HME was not made until late in the disease course. Investigations revealed cervical myelopathy due to vertebral exostosis as well as multiple exostoses in other sites. His gait was not improved after surgical decompression. A better knowledge of this disease could have prevented this neurological complication.
Pubmed
Web of science
Création de la notice
04/10/2011 15:09
Dernière modification de la notice
20/08/2019 14:31
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