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CEN Case Reports

, Volume 8, Issue 2, pp 79–82 | Cite as

Sarcoidosis in the renal allograft of a recipient whose primary disease was autosomal dominant polycystic kidney disease

  • Takahiro ShinzatoEmail author
  • Taro Kubo
  • Toshihiro Shimizu
  • Koji Nanmoku
  • Takashi Yagisawa
Case Report
  • 42 Downloads

Abstract

We report a 55-year-old man with a renal allograft that developed sarcoidosis. His autosomal dominant polycystic kidney disease (ADPKD) progressed to end-stage stage renal disease when he was 52 years old, and he underwent living-donor kidney transplantation at the age of 53 years. His proteinuria worsened at 19 months post-transplantation, and his renal function began to decline at 29 months post-transplantation. A renal allograft biopsy performed at 31 months post-transplantation revealed non-caseating granulomatous interstitial nephritis. The patient was treated with prednisolone (0.5 mg/kg/day), with gradual reduction in the dose. His proteinuria improved and renal function did not deteriorate any further. To the best of our knowledge, this is the first case of sarcoidosis in a renal allograft recipient whose primary renal disease was ADPKD.

Keywords

Sarcoidosis Kidney transplantation Autosomal dominant polycystic kidney disease 

Notes

Compliance with ethical standards

Conflict of interest

All the authors have declared no competing interest.

Human and animal rights

This article does not contain any studies with human participants performed by any of the authors.

Informed consent

Informed consent was obtained from all individual participants included in the study.

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Copyright information

© Japanese Society of Nephrology 2018

Authors and Affiliations

  1. 1.Department of Renal Surgery and TransplantationJichi Medical University HospitalShimotsukeJapan

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