Karyomegalic Interstitial Nephritis: Case Series and Review of Literature

Humaira Nasir, Nida Saleem, Fatima Anwar, Rabia Saleem, Rabia Saleem, Syed Nayer Mahmud

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Abstract

Karyomegalic interstitial nephritis(KIN) is a rare cause of hereditary interstitial nephritis, described 45 years ago. Only about 50 cases have been described in English literature so far and none from Pakistan. This disease has an escalated course with a worsened outcome. There are a few potential mimickers of this disease both clinically and histologically, which might lead to a missed diagnosis and hence poor management. We have described here a series of 05 cases of KIN that were diagnosed at our institute for a better understanding of this disease entity.
Original languageEnglish
Pages (from-to)693-697
Number of pages5
JournalAmerican Journal of Medical Case Reports
Volume9
Issue number12
DOIs
Publication statusPublished - 2021
Externally publishedYes

Keywords

  • interstitial nephritis
  • karyomegalic interstitial nephritis
  • chronic kidney disease
  • histopathology
  • kidney transplantation

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