Intravascular papillary endothelial hyperplasia of the central nervous system: Four case reports

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dc.contributor.authorÇagli S.
dc.contributor.authorOktar N.
dc.contributor.authorDalbasti T.
dc.contributor.authorIşlekel S.
dc.contributor.authorDemirtaş E.
dc.contributor.authorÖzdamar N.
dc.date.accessioned2019-10-27T08:59:26Z
dc.date.available2019-10-27T08:59:26Z
dc.date.issued2004
dc.departmentEge Üniversitesien_US
dc.description.abstractFour rare cases of intracranial intravascular papillary endothelial hyperplasia (IPEH) manifesting as cranial nerve disturbances occurred in 16-, 18-, 24-, and 28-year-old females. Magnetic resonance imaging showed all lesions as isointense with strong enhancement on T1-weighted images, and as hyperintense on T2-weighted images. All lesions were removed via craniotomies. Histological examination found vascular structures and papillary spaces lined with endothelial cells showing immunoreactivity for CD31. Complete removal was curative in two cases, whereas incomplete removal resulted in cure in one case and residual deficits in one case. Iatrogenic deficits should be avoided in IPEH treatment by surgery. Differentiation from neoplasm such as angiosarcoma depends on histological characteristics.en_US
dc.identifier.doi10.2176/nmc.44.302en_US
dc.identifier.endpage310en_US
dc.identifier.issn0470-8105
dc.identifier.issue6en_US
dc.identifier.pmid15253546en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage302en_US
dc.identifier.urihttps://doi.org/10.2176/nmc.44.302
dc.identifier.urihttps://hdl.handle.net/11454/27801
dc.identifier.volume44en_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.relation.ispartofNeurologia Medico-Chirurgicaen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCavernous sinusen_US
dc.subjectIntravascular papillary endothelial hyperplasiaen_US
dc.subjectPterional craniotomyen_US
dc.titleIntravascular papillary endothelial hyperplasia of the central nervous system: Four case reportsen_US
dc.typeArticleen_US

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