Adult langerhans cell histiocytosis

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dc.contributor.authorCil, Timucin
dc.contributor.authorGoekalp, Deniz
dc.contributor.authorTuzcu, Alparslan
dc.contributor.authorIsikdogan, Abdurrahman
dc.contributor.authorBahceci, Mithat
dc.date.accessioned2024-04-24T17:40:07Z
dc.date.available2024-04-24T17:40:07Z
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.en_US
dc.identifier.endpage635en_US
dc.identifier.issn1300-0292
dc.identifier.issue4en_US
dc.identifier.startpage633en_US
dc.identifier.urihttps://hdl.handle.net/11468/21623
dc.identifier.volume27en_US
dc.identifier.wosWOS:000254582700024
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.language.isotren_US
dc.publisherOrtadogu Ad Pres & Publ Coen_US
dc.relation.ispartofTurkiye Klinikleri Tip Bilimleri Dergisi
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBone And Bonesen_US
dc.subjectDiabetes Insipidusen_US
dc.titleAdult langerhans cell histiocytosisen_US
dc.titleAdult langerhans cell histiocytosis
dc.typeArticleen_US

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