Publication:
Endolymphatic sac tumor: a case report

dc.contributor.authorsInanli, S; Tutkun, A; Ozturk, O; Ahyskaly, R
dc.date.accessioned2022-03-12T16:59:39Z
dc.date.accessioned2026-01-11T19:02:37Z
dc.date.available2022-03-12T16:59:39Z
dc.date.issued2001
dc.description.abstractPapillary tumors of the temporal bone are aggressive neoplasms which may occur sporadically or as a part of von Hippel-Lindau disease. The term 'endolymphatic sac tumor' identifies the origin of these rare tumors. The clinical manifestations are sensorineural hearing loss, facial paralysis, cerebellar disorders and vertigo. The tumor is locally invasive, destructive and hypervascular exhibiting consistent imaging and histopathologic features. The treatment of choice is the total removal of the lesion although complete excision of the advanced lesion is nearly impossible due to the anatomic complexity of the endolymphatic sac and distinct patterns of extension. We present a 50-year-old male patient with endolymphatic sac tumor with left sided sensorineural hearing loss and review the literature. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
dc.identifier.doi10.1016/S0385-8146(01)00053-0
dc.identifier.eissn1879-1476
dc.identifier.issn0385-8146
dc.identifier.pubmed11489369
dc.identifier.urihttps://hdl.handle.net/11424/227221
dc.identifier.wosWOS:000170747700009
dc.language.isoeng
dc.publisherELSEVIER SCI LTD
dc.relation.ispartofAURIS NASUS LARYNX
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectendolymphatic sac tumor
dc.subjectpapillary tumor
dc.subjectvon Hippel-Lindau disease
dc.subjectHIPPEL-LINDAU-DISEASE
dc.subjectMIDDLE-EAR
dc.subjectADENOMA
dc.titleEndolymphatic sac tumor: a case report
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage248
oaire.citation.issue3
oaire.citation.startPage245
oaire.citation.titleAURIS NASUS LARYNX
oaire.citation.volume28

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