Spinal Schwannomatosis Unassociated with Phakomatosis: A Case Report

dc.contributor.authorBadejo, O. A.
dc.contributor.authorNwafuluaku, E. C.
dc.contributor.authorSalami, A. A.
dc.date.accessioned2026-04-14T08:51:53Z
dc.date.issued2021
dc.description.abstractSchwannomas are slow-growing, encapsulated benign tumors of the peripheral nerves. The multiplicity of these tumors has been linked with genetic anomalies associated with neurofibromatosis. Schwannomatosis is a rare autosomal-dominant tumor syndrome characterized by the occurrence of multiple schwannomas of the peripheral nervous system, with no involvement of the vestibular nerve. This contrasts with neurofibromatosis 2, in which the existence of bilateral vestibular schwannomas is pathognomonic. Spinal schwannomatosis without features of neurofibromatosis is a very rare occurrence, previously unreported in Nigerian neurosurgical literature. We present a Nigerian patient with cervical intradural-extramedullary and thoracic intramedullary spinal schwannomas. His treatment outcome and a brief literature review were also discussed.
dc.identifier.issn2811-1826
dc.identifier.otherui_art_badejo_spinal_2021
dc.identifier.otherArchives of Neurosurgery in africa 2(2), pp. 29-34
dc.identifier.urihttps://repository.ibadanedu.com/handle/123456789/13711
dc.language.isoen
dc.publisherSamdavies Publishers, His Grace Villa, Plot 4, Adenekan-Oyejide Street, Oloruntedo Layout, Kuelu, Olode, New Ife Road, Ibadan, Nigeria.
dc.subjectSchwannomas
dc.subjectCongenital neurilemmomatosis
dc.subjectIntradural tumors
dc.subjectNeurofibromatosis type
dc.titleSpinal Schwannomatosis Unassociated with Phakomatosis: A Case Report
dc.typeArticle

Files

Original bundle

Now showing 1 - 1 of 1
Thumbnail Image
Name:
(36) ui_art_badejo_spinal_2021.pdf
Size:
1.71 MB
Format:
Adobe Portable Document Format

License bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.61 KB
Format:
Item-specific license agreed upon to submission
Description: