Publication:
Hemangioblastoma of the spinal nerve root

dc.contributor.authorsPeker S., Sun I., Özgen S., Kurtkaya-Yapicier Ö., Pamir M.N.
dc.date.accessioned2022-03-28T14:51:48Z
dc.date.accessioned2026-01-11T19:04:06Z
dc.date.available2022-03-28T14:51:48Z
dc.date.issued2003
dc.description.abstractSpinal root haemangioblastomas are very rare tumors. A 70-year-old male patient admitted to our clinic with low back and both legs pain of one year's duration. Magnetic resonance imaging revealed a solid mass lesion at T-12 level. The contrast enhancing mass was intradural in location. T-12 laminectomy was performed and a highly vascular mass originated at the T-12 nerve root was totally removed. Histopathological examination revealed diagnosis of haemangioblastoma. He was then screened for von Hippel Lindau disease. No stigmata of this disease were found. The postoperative period was uneventful. He was discharged with no complaints. Spinal root haemangioblastoma should be kept in mind in a patient with highly enhancing spinal intradural mass.
dc.identifier.issn10191941
dc.identifier.urihttps://hdl.handle.net/11424/255747
dc.language.isoeng
dc.relation.ispartofMarmara Medical Journal
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectHemangioblastoma
dc.subjectSpinal nerve root
dc.subjectVon Hippel Lindau disease
dc.titleHemangioblastoma of the spinal nerve root
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage221
oaire.citation.issue3
oaire.citation.startPage219
oaire.citation.titleMarmara Medical Journal
oaire.citation.volume16

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