Hemophagocytic Syndrome in a Patient with Adult-onset Still's Disease

Basit Öğe Kaydı
dc.contributor.authorÇalık, Yalkın
dc.contributor.authorAtaoğlu, Safinaz
dc.contributor.authorBaş, Ersun
dc.contributor.authorYazıcı, Selma
dc.contributor.authorBaki, Ali Erdem
dc.contributor.authorYavuz, Metin
dc.date.accessioned2020-05-01T12:10:19Z
dc.date.available2020-05-01T12:10:19Z
dc.date.issued2011
dc.departmentDÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.descriptionWOS: 000295972800009en_US
dc.description.abstractHemophagocytic syndrome is a fatal and life-threatening syndrome characterized by pancytopenia and multiple organ failure. It can frequently be seen in childhood as a primary or familial condition. In adults, it occurs secondarily. In etiology, wide range of factors are related to this syndrome. Adult-onset Still's disease seems to be one of the systemic rheumatological diseases that cause this syndrome. In our literature review, we found few studies related to this syndrome. In this article, we report a 40-year-old female patient who had been treated with the diagnosis of Adult-onset Still's disease for four years in our clinic and who developed hemophagocytic syndrome during her follow-ups.en_US
dc.identifier.doi10.5606/tjr.2011.022en_US
dc.identifier.endpage153en_US
dc.identifier.issn1309-0291
dc.identifier.issue2en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage150en_US
dc.identifier.urihttps://doi.org/10.5606/tjr.2011.022
dc.identifier.urihttps://hdl.handle.net/20.500.12684/6138
dc.identifier.volume26en_US
dc.identifier.wosWOS:000295972800009en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakTR-Dizinen_US
dc.language.isoenen_US
dc.publisherTurkish League Against Rheumatismen_US
dc.relation.ispartofTurkish Journal Of Rheumatologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAdult-onset still's diseaseen_US
dc.subjecthemophagocytic syndromeen_US
dc.subjecthemophagocytosisen_US
dc.titleHemophagocytic Syndrome in a Patient with Adult-onset Still's Diseaseen_US
dc.typeArticleen_US

Dosyalar

Orijinal paket
Listeleniyor 1 - 1 / 1
Küçük Resim
İsim:
6138.pdf
Boyut:
2.3 MB
Biçim:
Adobe Portable Document Format
Açıklama:
Tam Metin / Full Text
İndir

Koleksiyon

WoS İndeksli Yayınlar Koleksiyonu
Makale Koleksiyonu
Scopus İndeksli Yayınlar Koleksiyonu
TR-Dizin İndeksli Yayınlar Koleksiyonu