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Ann Pathol. 2010 Jun;30(3):240-2. doi: 10.1016/j.annpat.2010.03.001. Epub 2010 Apr 14.

[Karyomegalic interstitial nephritis: A new French case].

[Article in French]

Author information

  • 1hôpital Saint-Louis, AP-HP, Paris, France. jerome.verine@sls.aphp.fr

Abstract

Karyomegalic interstitial nephritis (KIN) is a rare and slowly progressive chronic interstitial nephritis (CIN) (28 cases reported), described for the first time by Mihatsch et al. in 1979. Here, we report on a 50-year-old woman who presented with asymptomatic renal failure and mild proteinuria without hematuria. Renal biopsy showed large tubulo-interstitial fibrosis and massively enlarged tubular epithelial cell nuclei, without viral inclusion. KIN is a rare CIN defined by a karyomegaly of tubular epithelial cell nuclei. Its pathogenesis remains obscure. Nevertheless, an exogenous factor is suspected, ochratoxin A particularly. The familial clustering of patients and the frequency of HLA-A9 and HLA-B35 haplotypes suggest the presence of a possible genetic susceptibility to this disorder.

2010 Elsevier Masson SAS. All rights reserved.

PMID:
20621605
[PubMed - indexed for MEDLINE]
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