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dc.contributor.authorMert, A
dc.contributor.authorPamuk, Gizem
dc.contributor.authorPamuk, ON
dc.contributor.authorAktuglu, Y
dc.contributor.authorTabak, F
dc.contributor.authorAltiparmak, MR
dc.date.accessioned2021-03-05T14:26:25Z
dc.date.available2021-03-05T14:26:25Z
dc.date.issued2001
dc.identifier.citationAltiparmak M., Tabak F., Pamuk O., Pamuk G., Mert A., Aktuglu Y., "Giant cell arteritis and secondary amyloidosis: the natural history", SCANDINAVIAN JOURNAL OF RHEUMATOLOGY, cilt.30, ss.114-116, 2001
dc.identifier.issn0300-9742
dc.identifier.otherav_b71b0bd6-42e8-4f26-a9d8-b57548514c98
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/121881
dc.identifier.urihttps://doi.org/10.1080/03009740151095448
dc.description.abstractGiant cell (temporal) arteritis (GCA) may be a cause of fever of unknown origin (FUO) in elderly patients. The development of secondary (reactive) amyloidosis is an unusual complication of the disease, we describe a 65-year-old male patient who was hospitalized in our hospital with FUO and was diagnosed as having GCA 5 years later. At that time, he also had a nephrotic syndrome and secondary amyloidosis (AA-type). He died due to end-stage renal failure. The probable explanation for the development of this rare complication might be the late diagnosis of this chronic inflammatory disease, which was left untreated for a long period of time.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectİmmünoloji ve Romatoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectROMATOLOJİ
dc.titleGiant cell arteritis and secondary amyloidosis: the natural history
dc.typeMakale
dc.relation.journalSCANDINAVIAN JOURNAL OF RHEUMATOLOGY
dc.contributor.department, ,
dc.identifier.volume30
dc.identifier.issue2
dc.identifier.startpage114
dc.identifier.endpage116
dc.contributor.firstauthorID41097


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