Familial Wilms' tumor: a descriptive study

Med Pediatr Oncol. 1996 Nov;27(5):398-403. doi: 10.1002/(SICI)1096-911X(199611)27:5<398::AID-MPO2>3.0.CO;2-H.


Among 6,209 patients with Wilms' tumor entered on the National Wilms' Tumor Study (NWTS), 93 patients (1.5%) from 63 families had a positive family history. In 30 of these 63 families a (half) sibling or parent of the NWTS patient was confirmed to have had Wilms' tumor. Fifteen (16.1%) of the familial, but only 7.1% of sporadic cases, had bilateral disease. Mean ages at diagnosis were 15.8 vs. 35.2 months (P = 0.012) for bilateral vs. unilateral familial cases and 32.0 vs. 44.7 months for sporadic cases. Intralobar nephrogenic rests were found twice as frequently in association with the tumors of familial as with those of sporadic cases. Cases of bilateral and metastatic disease tended to cluster within specific families, suggesting heterogeneity in the genetic etiology. The number and age distribution of familial cases transmitted through the father were about the same as those of cases transmitted through the mother. This finding is inconsistent with models of genomic imprinting that involve familial transmission of a tumor-suppressor gene and it casts further doubt on the hypothesis that all bilateral cases are hereditary.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Age Distribution
  • Age Factors
  • Child
  • Child, Preschool
  • Female
  • Follow-Up Studies
  • Genes, Wilms Tumor / genetics
  • Genomic Imprinting
  • Humans
  • Infant
  • Kidney Neoplasms / genetics*
  • Kidney Neoplasms / pathology
  • Male
  • Neoplasm Staging
  • Registries
  • Survival Rate
  • Treatment Outcome
  • Wilms Tumor / genetics*
  • Wilms Tumor / pathology
  • X Chromosome / genetics
  • Y Chromosome / genetics