Literature DB >> 24315002

Kidney transplantation in hereditary coproporphyria using tacrolimus and mycophenolate mofetil: a case report.

G Telkes1, A Pusztai, K Földes, R M Langer.   

Abstract

BACKGROUND: The porphyrias are a group of disorders of the heme biosynthesis pathway that may present with acute life-threatening attacks, commonly exacerbated by a wide variety of medications. Many newer immunosuppressive medications, which are in use following kidney transplantation, have not been fully explored in acute porphyrias. CASE REPORT: A 53-year-old woman received a kidney from a deceased donor, after being on hemodialysis for 4 years. Hereditary coproporphyria was diagnosed at age 19 years. We administered tacrolimus, mycophenolate mofetil and steroid immunosuppression. In the immediate post-transplant periods she displayed abdominal pain and transient uroporphyrin elevation in parallel with slightly elevated (15 ng/mL) tacrolimus concentrations. As the target tacrolimus level was achieved, these findings disappeared.
CONCLUSIONS: Tacrolimus, mycophenolate- mofetil, and steroid therapy for hereditery coproporphyri was safe, in the long term.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 24315002     DOI: 10.1016/j.transproceed.2013.10.008

Source DB:  PubMed          Journal:  Transplant Proc        ISSN: 0041-1345            Impact factor:   1.066


  1 in total

1.  Diagnosis of acute intermittent porphyria in a renal transplant patient: A case report.

Authors:  Cristina Sirch; Niloufar Khanna; Lynda Frassetto; Francesco Bianco; Mary Louise Artero
Journal:  World J Transplant       Date:  2022-01-18
  1 in total

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