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dc.contributor.authorKasapoğlu, Umut
dc.contributor.authorRuhi, Çağlar
dc.contributor.authorTuğcu, Murat
dc.contributor.authorBoynueğri, Başak
dc.contributor.authorTitiz, İzzet
dc.contributor.authorHançer, Veysel Sabri
dc.contributor.authorApaydın, Süheyla
dc.date.accessioned2016-03-26T10:11:37Z
dc.date.available2016-03-26T10:11:37Z
dc.date.issued2015
dc.identifier.citationKasapoglu U, Ruhi C, Tugcu M, Boynuegri B, Titiz I, Hancer VS, Apaydin S. Prophylactic Eculizumab Use in Kidney Transplantation: A Review of the Literature and Report of a Case with Atypical Hemolytic Uremic Syndrome. Ann Transplant. 2015 Dec 1;20:714-719. doi: 10.12659/AOT.894665en_US
dc.identifier.issn1425-9524
dc.identifier.urihttp://www.annalsoftransplantation.com/en_US
dc.identifier.urihttps://hdl.handle.net/11446/929en_US
dc.descriptionİstanbul Bilim Üniversitesi, Tıp Fakültesi.en_US
dc.description.abstractBackground: Atypical hemolytic uremic syndrome (aHUS) is a very rare disease, which presents with microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury. Progression to end-stage renal disease (ESRD) from acute kidney injury is observed in 60% of aHUS cases. The prognosis of aHUS patients who undergo kidney transplantation (Ktx) is generally poor, but these patients should be treated prophylactically with eculizumab to prevent recurrence after transplantation. Case Report: An 18-year-old man was referred to our center with a history of rapid progression to ESRD with unknown etiology. He had anemia, thrombocytopenia, high levels of LDH, and indirect bilirubin and creatinine on initial laboratory results. Our diagnosis was aHUS due to initial results, normal level of ADAMTS activity, and lack of predisposing factors seen in typical HUS. We planned to perform genetic analysis for the patient and the donor candidate (mother). The variations found on exon 7 of the CFH gene had not been reported previously. According to PolyPhen analysis, this mutation was reported as a potential cause for aHUS. We decided to perform Ktx under eculizumab prophylaxis. Weekly administration of prophylaxis was extended to 1 month. The graft functioned immediately after Ktx. The patient has completed his first year uneventfully in our follow-up, with a creatinine 0.79 mg/dl at his last control visit.en_US
dc.language.isoengen_US
dc.publisherSpringer Verlagen_US
dc.identifier.doi10.12659/AOT.894665en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectcomplement C5en_US
dc.subjecthemolytic-uremic syndromeen_US
dc.subjectkidney transplantationen_US
dc.titleProphylactic eculizumab use in kidney transplantation: A review of the literature and report of a case with atypical hemolytic uremic syndrome.en_US
dc.typearticleen_US
dc.relation.journalAnnals of Transplantationen_US
dc.departmentDBÜ, Tıp Fakültesien_US
dc.identifier.volume20
dc.identifier.startpage714
dc.identifier.endpage719
dc.contributor.authorIDTR238826en_US
dc.contributor.authorIDTR175369en_US
dc.contributor.authorIDTR233013en_US
dc.contributor.authorIDTR43513en_US
dc.contributor.authorIDTR130188en_US
dc.relation.publicationcategoryBelirsizen_US


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