Literature DB >> 10751059

Recurrence of IgA nephropathy 17 months after renal transplantation in the allograft transmitted thin basement membrane disease (TBMD) from donor.

Y Nakagawa1, K Saito, S Nishi, V Bilim, T Tanikawa, M Ueno, H Shimada, Y Osawa, M Arakawa, K Takahashi.   

Abstract

Recurrence of IgA nephropathy (IgAN) following renal transplantation has been described in 40-50% of such patients and it usually has a good outcome. We present the case of a 20-yr-old woman with IgAN who developed end-stage renal failure in 1995. In November 1996, she received a kidney from a living-related donor and was treated with tacrolimus, azathioprine and steroids. Zero- and one-hour biopsies were performed, which revealed minor glomerular abnormalities in light microscopy, thin basement membrane disease (TBMD) in electron microscopy. Eight months later she developed microscopic hematuria and proteinuria; however, the graft function was normal. Renal biopsy revealed an IgAN that is thought to be due to recurrence of the original disease.

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Year:  1999        PMID: 10751059

Source DB:  PubMed          Journal:  Clin Transplant        ISSN: 0902-0063            Impact factor:   2.863


  1 in total

1.  Defective activation of the MAPK/ERK pathway, leading to PARP1 and DNMT1 dysregulation, is a common defect in IgA nephropathy and Henoch-Schönlein purpura.

Authors:  Annamaria Milillo; Clelia Molinario; Stefano Costanzi; Gisella Vischini; Francesca La Carpia; Francesco La Greca; Donato Rigante; Giovanni Gambaro; Fiorella Gurrieri; Eugenio Sangiorgi
Journal:  J Nephrol       Date:  2018-03-01       Impact factor: 3.902

  1 in total

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