Adult langerhans cell histiocytosis: Differential diagnosis

dc.contributor.authorÇil T.
dc.contributor.authorGökalp D.
dc.contributor.authorTuzcu A.
dc.contributor.authorIşikdoğan A.
dc.contributor.authorBahçeci M.
dc.date.accessioned2024-04-24T18:43:38Z
dc.date.available2024-04-24T18:43:38Z
dc.date.issued2007
dc.departmentDicle Üniversitesien_US
dc.description.abstractLangerhans cell histiocytosis is a group of idiopathic disorders characterized by the abnormal proliferation of specialized bone marrow-derived Langerhans cells. There are one to two cases per million population. Most reports are based only on anecdotal experience in adult patients. Surgical excision, radiotherapy and chemotherapy, either alone or in combination are the main treatment options. In this report, we present a rare case of Langerhans cell histiocytosis in a 32 years-old-woman who developed symptomatic diabetes insipidus and multiple bone and cranial metastases during the disease course. This paper discusses controversial treatment modalities. Copyright © 2007 by Türkiye Klinikleri.en_US
dc.identifier.endpage635en_US
dc.identifier.issn1300-0292
dc.identifier.issue4en_US
dc.identifier.scopus2-s2.0-34948907304
dc.identifier.scopusqualityQ4
dc.identifier.startpage633en_US
dc.identifier.urihttps://hdl.handle.net/11468/24232
dc.identifier.volume27en_US
dc.indekslendigikaynakScopus
dc.language.isotren_US
dc.publisherTurkiye Kliniklerien_US
dc.relation.ispartofTurkiye Klinikleri Journal of Medical Sciences
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBone And Bonesen_US
dc.subjectDiabetes İnsipidusen_US
dc.titleAdult langerhans cell histiocytosis: Differential diagnosisen_US
dc.titleAdult langerhans cell histiocytosis: Differential diagnosis
dc.title.alternativeYetişkin langerhans hücreli histiyositozen_US
dc.title.alternativeYetişkin langerhans hücreli histiyositoz
dc.typeArticleen_US

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