Early presentation of bilateral gonadoblastomas in a Denys-Drash syndrome patient: a cautionary tale for prophylactic gonadectomy

J Pediatr Endocrinol Metab. 2013;26(9-10):971-4. doi: 10.1515/jpem-2012-0409.

Abstract

Mutation of the Wilms tumor gene (WT1) is associated with two well-described syndromes called Denys-Drash (DDS) and Frasier (FS). Both are associated with nephropathy and ambiguous genitalia and have overlapping clinical and molecular features. The known risk of Wilms tumor in DDS and gonadoblastoma (GB) in FS patients requires tumor surveillance. The literature reports the occurrence of GB in DDS as lower than FS. This case highlights a very early presentation of bilateral GB in DDS and the consideration of early prophylactic gonadectomy at the time of diagnosis with DDS.

Publication types

  • Case Reports

MeSH terms

  • Amino Acid Substitution
  • Denys-Drash Syndrome / genetics
  • Denys-Drash Syndrome / pathology
  • Denys-Drash Syndrome / physiopathology*
  • Disease Progression
  • Early Detection of Cancer*
  • Exons
  • Family
  • Female
  • Gender Identity
  • Genetic Counseling
  • Gonadoblastoma / diagnosis
  • Gonadoblastoma / etiology*
  • Gonadoblastoma / surgery
  • Gonads / pathology
  • Gonads / surgery
  • Humans
  • Incidental Findings*
  • Infant
  • Kidney Failure, Chronic / etiology
  • Male
  • Mutation, Missense
  • Sex Reassignment Surgery
  • Testicular Neoplasms / diagnosis
  • Testicular Neoplasms / etiology*
  • Testicular Neoplasms / surgery
  • WT1 Proteins / genetics

Substances

  • WT1 Proteins
  • WT1 protein, human