Correlation between Papilledema and Intracranial Hypertension in Crouzon Syndrome: A Case Report and Review of the Literature.

Détails

ID Serval
serval:BIB_17493CFDE8B8
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Synthèse (review): revue aussi complète que possible des connaissances sur un sujet, rédigée à partir de l'analyse exhaustive des travaux publiés.
Collection
Publications
Institution
Titre
Correlation between Papilledema and Intracranial Hypertension in Crouzon Syndrome: A Case Report and Review of the Literature.
Périodique
Pediatric neurosurgery
Auteur(s)
Simonin A., Maduri R., Viaroli E., Levivier M., Daniel R.T., Messerer M.
ISSN
1423-0305 (Electronic)
ISSN-L
1016-2291
Statut éditorial
Publié
Date de publication
2019
Peer-reviewed
Oui
Volume
54
Numéro
4
Pages
223-227
Langue
anglais
Notes
Publication types: Case Reports ; Journal Article ; Review
Publication Status: ppublish
Résumé
Crouzon syndrome represents the most common syndromic craniosynostosis. Ocular complications are frequent, including papilledema and optic atrophy, often related to increased intracranial pressure (ICP). However, there is a poor correlation between ICP normalization and resolution of papilledema. We describe the case of a 6-month-old infant who presented with typical phenotypic features of Crouzon syndrome. Pre- and postoperative ICP monitoring was used. Papilledema persisted despite ICP improvement after decompressive craniectomy. Possible causes of papilledema in this syndromic craniosynostosis are discussed in light of the existing literature.
Mots-clé
Craniofacial Dysostosis/complications, Craniofacial Dysostosis/surgery, Craniosynostoses/complications, Craniosynostoses/surgery, Decompression, Surgical, Humans, Infant, Intracranial Hypertension/etiology, Magnetic Resonance Imaging, Male, Papilledema/etiology, Phenotype, Ultrasonography, Craniosynostosis, Crouzon syndrome, Intracranial hypertension, Papilledema
Pubmed
Web of science
Création de la notice
08/07/2019 15:19
Dernière modification de la notice
30/01/2020 6:20
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