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dc.contributor.authorYetiser, S
dc.contributor.authorCekin, E
dc.contributor.authorTosun, N
dc.contributor.authorYildirim, A
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T10:22:38Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T10:22:38Z
dc.date.issued2004
dc.identifier.issn0165-5876
dc.identifier.urihttps://dx.doi.org/10.1016/j.ijporl.2004.03.014
dc.identifier.urihttps://hdl.handle.net/20.500.12418/11180
dc.descriptionWOS: 000223244200016en_US
dc.descriptionPubMed ID: 15236900en_US
dc.description.abstractRosai-Dorfman disease (RDD) is an uncommon pathologic condition of unknown ethiotogy with an idiopathic proliferation of the hystiocytes. It is generally presented with massive bilateral hypertrophy of the cervical lymph nodes. But other lymph nodes may also be involved. Approximately, 30% of these patients have extra nodal mass or lesion with different signs or symptoms depending on localization. We present two mate siblings with Rosai-Dorfman disease who have classical cervical lymphadenopathy associated with progressive neurosensorial hearing toss and dural-based intracranial lesions. (C) 2004 Elsevier Ireland Ltd. All rights reserved.en_US
dc.language.isoengen_US
dc.publisherELSEVIER SCI IRELAND LTDen_US
dc.relation.isversionof10.1016/j.ijporl.2004.03.014en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectRosai-Dorfman diseaseen_US
dc.subjecthearing lossen_US
dc.subjectintracranial dural lesionen_US
dc.titleRosai-Dorfman disease associated with neurosensorial hearing loss in two siblingsen_US
dc.typearticleen_US
dc.relation.journalINTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGYen_US
dc.contributor.departmentGulhane Med Sch, Dept ORL & HNS, TR-06018 Ankara, Turkey -- Cumhuriyet Univ, Dept ORL & HNS, Sivas, Turkeyen_US
dc.identifier.volume68en_US
dc.identifier.issue8en_US
dc.identifier.endpage1100en_US
dc.identifier.startpage1095en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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