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Transplant Proc ; 50(2): 572-574, 2018 Mar.
Article in English | MEDLINE | ID: mdl-29579855

ABSTRACT

A high rate of recurrence has been described in atypical hemolytic uremic syndrome renal transplant recipients, favored by certain immunosuppressant drugs that can induce complement activation. We present four case series in which three patients were diagnosed pretransplantation and a fourth who had onset in the very early post-transplantation period. The patients received different immunosuppression schedules, and all had improvement after more than 2-years. We suggest the need to stratify the risk of atypical hemolytic uremic syndrome recurrence using genetic studies and the available drugs as the main factors that allow graft survival improvement today.


Subject(s)
Atypical Hemolytic Uremic Syndrome/immunology , Immunosuppression Therapy/adverse effects , Kidney Transplantation/adverse effects , Postoperative Complications/immunology , Adult , Aged , Atypical Hemolytic Uremic Syndrome/surgery , Complement Activation , Female , Graft Survival/immunology , Humans , Immunosuppression Therapy/methods , Kidney/immunology , Male , Middle Aged , Recurrence , Risk Factors
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