Basit öğe kaydını göster

dc.contributor.authorAkpolat, T
dc.contributor.authorAkpolat, I
dc.contributor.authorKandemir, B
dc.date.accessioned2020-06-21T15:50:06Z
dc.date.available2020-06-21T15:50:06Z
dc.date.issued2000
dc.identifier.issn0250-8095
dc.identifier.issn1421-9670
dc.identifier.urihttps://doi.org/10.1159/000013559
dc.identifier.urihttps://hdl.handle.net/20.500.12712/22357
dc.descriptionWOS: 000084953200012en_US
dc.descriptionPubMed: 10644872en_US
dc.description.abstractBehcet's disease (BD) is a multisystem disorder characterized by vasculitis. To our knowledge, 52 patients with ED and amyloidosis have previously been described in the literature. Nephrotic syndrome was the most common type of presentation of amyloidosis in these patients. The prognosis of patients with ED and amyloidosis has not been reported before, in this report, we present a patient with ED and AA-type amyloidosis and analyze the prognosis in these patients, Follow-up and prognosis have been reported in 23 patients. Ten of these 23 patients died and most of these deaths occurred within 3 months after the diagnosis of amyloidosis, Endstage renal disease developed shortly in 4 patients, ED should be considered in the differential diagnosis of AA amyloidosis. In conclusion, the cases with ED and amyloidosis carry poor prognosis. Copyright (C) 2000 S. Karger AG, Basel.en_US
dc.language.isoengen_US
dc.publisherKargeren_US
dc.relation.isversionof10.1159/000013559en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBehcet's diseaseen_US
dc.subjectamyloidosisen_US
dc.subjectprognosisen_US
dc.titleBehcet's disease and AA-type amyloidosisen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume20en_US
dc.identifier.issue1en_US
dc.identifier.startpage68en_US
dc.identifier.endpage70en_US
dc.relation.journalAmerican Journal of Nephrologyen_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