| Literature DB >> 25864519 |
Anuja Java1, Angelina Edwards1, Ana Rossi1, Richa Pandey1, Joseph Gaut2, Rowena Delos Santos1, Brent Miller1, Christina Klein1, Daniel Brennan1.
Abstract
De novo thrombotic microangiopathy (TMA) after renal transplant is rare. Cytomegalovirus (CMV)-related post-transplant TMA has only been reported in 6 cases. We report an unusual case of a 75-year-old woman who developed de novo TMA in association with CMV viremia. The recurrence of TMA with CMV viremia, the resolution with treatment for CMV, and the lack of correlation with a calcineurin inhibitor (CNI) in our case support CMV as the cause of the TMA. What is unique is that the use of eculizumab without plasmapheresis led to prompt improvement in renal function. After a failure to identify a genetic cause for TMA and the clear association with CMV, eculizumab was discontinued. This case provides insight into the pathogenesis and novel treatment of de novo TMA, highlights the beneficial effects of complement inhibitors in this disease, and shows that they can be safely discontinued once the inciting etiology is addressed.Entities:
Keywords: atypical hemolytic uremic syndrome; cytomegalovirus; eculizumab; renal transplant thrombotic microangiopathy
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Year: 2015 PMID: 25864519 PMCID: PMC4529787 DOI: 10.1111/tri.12582
Source DB: PubMed Journal: Transpl Int ISSN: 0934-0874 Impact factor: 3.782