TY - JOUR
T1 - Cytomegalovirus-induced thrombotic microangiopathy after renal transplant successfully treated with eculizumab
T2 - Case report and review of the literature
AU - Java, Anuja
AU - Edwards, Angelina
AU - Rossi, Ana
AU - Pandey, Richa
AU - Gaut, Joseph
AU - Delos Santos, Rowena
AU - Miller, Brent
AU - Klein, Christina
AU - Brennan, Daniel
N1 - Publisher Copyright:
© 2015 Steunstichting ESOT.
PY - 2015/9/1
Y1 - 2015/9/1
N2 - Summary 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.
AB - Summary 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.
KW - atypical hemolytic uremic syndrome
KW - cytomegalovirus
KW - eculizumab
KW - renal transplant thrombotic microangiopathy
UR - http://www.scopus.com/inward/record.url?scp=84938743746&partnerID=8YFLogxK
U2 - 10.1111/tri.12582
DO - 10.1111/tri.12582
M3 - Review article
C2 - 25864519
AN - SCOPUS:84938743746
SN - 0934-0874
VL - 28
SP - 1121
EP - 1125
JO - Transplant International
JF - Transplant International
IS - 9
ER -