Abstract
Atypical hemolytic uremic syndrome (aHUS) has gained increased visibility over several years as an important cause of renal failure. Unfortunately, diagnosis is often difficult because individual courses can be highly variable depending the causative genetic mutations. Here we present the case of a patient with a failed renal allograft and acute failure of a second allograft who was ultimately diagnosed with aHUS. Interestingly, he developed early de novo donor specific antibodies (DSA) after the second renal transplant in context of likely recurrent aHUS. Terminal complement inhibition with eculizumab resulted in prompt improvement of renal allograft function.
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Notes
Recipient HLA typing was as follows: A11, A24, B18, B35, DR4, DR53 (there was no C, DQ or DP tying for the recipient). Donor HLA typing was as follows: A2, A68, B53, C4, DR13, DR16, DQ2, and DQ5 (there was no donor DP typing).
Recipient HLA typing was as follows: A11, A24, B18, B35, DR4, DR53 (there was no C, DQ or DP tying for the recipient). Donor HLA typing was as follows: A1, A24, B7, B62, C7, C10, DR4, DR53, DQ8, DP3, and DP14. There was no history of Class II donor specific antibodies pre- or post-transplant.
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Acknowledgements
We would specifically like to thank Lisa Scholz, RN, MS for her continuity care of this patient. The authors would like to thank the faculty and staff of the Comprehensive Transplant Center of Northwestern Memorial Hospital.
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Dr. Gallon has a consulting and advisory relationship with Alexion Pharmaceuticals, Inc. The other authors declare no conflicts of interest.
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Zwang, N.A., Ho, B., Kanwar, Y.S. et al. A case of atypical hemolytic uremic syndrome in a second renal transplant. J Nephrol 31, 165–172 (2018). https://doi.org/10.1007/s40620-016-0373-7
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DOI: https://doi.org/10.1007/s40620-016-0373-7