BMC Nephrology (May 2023)

Karyomegalic interstitial nephritis as a rare cause of kidney graft dysfunction: case report and review of literature

  • Fatma El-Husseiny Moustafa,
  • Eman Nagy,
  • Salwa Mahmoud Elwasif,
  • Mohamed Sobh

DOI
https://doi.org/10.1186/s12882-023-03185-3
Journal volume & issue
Vol. 24, no. 1
pp. 1 – 6

Abstract

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Abstract Karyomegalic interstitial nephritis (KIN) is a rare cause of chronic interstitial nephritis characterized by enlarged renal tubular epithelial nuclei. The first case of KIN reported in a kidney graft was in 2019. Here, we report the first case of KIN in 2 brothers receiving kidneys from 2 different unrelated living donors. A male kidney transplant recipient with focal segmental glomerulosclerosis as the original kidney disease presented with graft impairment and proteinuria, and graft biopsy revealed KIN. This patient had a brother who was also a kidney transplant recipient and had one episode of graft impairment and was diagnosed with KIN as well.

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