Paediatric Cavernous Malformation of the Trigeminal Nerve: Case Report and Review of the Literature.
Cavernoma
Cerebellopontine angle
Trigeminal nerve
Journal
Pediatric neurosurgery
ISSN: 1423-0305
Titre abrégé: Pediatr Neurosurg
Pays: Switzerland
ID NLM: 9114967
Informations de publication
Date de publication:
2022
2022
Historique:
received:
06
07
2021
accepted:
06
04
2022
pubmed:
11
4
2022
medline:
23
6
2022
entrez:
10
4
2022
Statut:
ppublish
Résumé
Intradural, extra-axial cerebral cavernous malformations (CCMs) are rare entities and are mostly reported in relation to the optic apparatus or the facial/vestibulocochlear complex. Cranial nerve CCMs tend to follow a clinically aggressive course, with a tendency to progressive neurological dysfunction following intra-lesional haemorrhage or less commonly due to the effects of subarachnoid haemorrhage. We report the first case of a trigeminal CCM presenting in a child with otalgia and left-sided headaches. The patient was initially managed with radiological surveillance but required surgical management following deterioration. We describe the successful treatment of the lesion with microsurgical resection. A CCM should be considered in the differential diagnosis of mass lesions arising in the region of the trigeminal nerve. Surgical resection is recommended to prevent neurological deterioration and may result in significant symptomatic improvement.
Identifiants
pubmed: 35398849
pii: 000524522
doi: 10.1159/000524522
doi:
Types de publication
Case Reports
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
207-212Informations de copyright
© 2022 S. Karger AG, Basel.