Basit öğe kaydını göster

dc.contributor.authorKandemir B.
dc.contributor.authorKefeli M.
dc.contributor.authorYildiz L.
dc.contributor.authorKaragöz F.
dc.date.accessioned2020-06-21T09:23:24Z
dc.date.available2020-06-21T09:23:24Z
dc.date.issued2005
dc.identifier.issn1300-2996
dc.identifier.urihttps://hdl.handle.net/20.500.12712/3540
dc.description.abstractKimura disease is a benign chronic inflammatory disorder of unknown etiology. It was firstly reported by Kimm and Szeto in 1937 and was termed as eosinophilic hyperplastic lymphogranuloma. The definitive description was published by Kimura et al in 1948 and took its place as Kimura disease in the literature. It appears as a lymphadenopathy or mass in the region of head and neck and chracterized by prominent germinal centers and eosinophilic infiltration .This condition is very rare and its true importance lies in its ability to mimic a number of other inflammatory and neoplastic conditions. In our report histopatological and clinical features of a case diagnosed as Kimura disease were discussed with the literature findings.en_US
dc.language.isoturen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectEosinophilic infiltrationen_US
dc.subjectKimura diseaseen_US
dc.subjectLymphadenopathyen_US
dc.titleKimura disease: Case reporten_US
dc.title.alternativeKimura hastaliği: Olgu sunumuen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume22en_US
dc.identifier.issue3en_US
dc.identifier.startpage135en_US
dc.identifier.endpage138en_US
dc.relation.journalOndokuz Mayis Universitesi Tip Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


Bu öğenin dosyaları:

DosyalarBoyutBiçimGöster

Bu öğe ile ilişkili dosya yok.

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster