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Wilms' tumour associated with deep cystic nephroma‐like changes: three cases of a putative Wilms' tumour precursor

  • N. WALFORD*
  • , J. F. M. DELEMARRE
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

We describe three cases of Wilms' tumour accompanied by central pericalyceal multicystic lesions closely resembling those seen in cystic nephroma. In continuity with these lesions or elsewhere in the kidney were areas of dydysplastic renal tissue of the type sometimes referred to as intralobar nephroblastomatosis. A close homology of tissue differentiation was observed between the dysplastic lesions and the interstitial components of the cystic lesion. These findings support the hypothesis that, in some cases at least, cystic nephroma has more in common with the group of dysplastic lesions referred to as the nephroblastomatosis complex than with the true renal tumours of childhood. Copyright © 1991, Wiley Blackwell. All rights reserved
Original languageEnglish
Pages (from-to)123-131
JournalHistopathology
Volume18
Issue number2
DOIs
Publication statusPublished - 1991
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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