An Atypical Case of Very Early-onset Familial Adenomatous Polyposis Associated With Focal Cortical Dysplasia

J Pediatr Hematol Oncol. 2022 Apr 1;44(3):e743-e746. doi: 10.1097/MPH.0000000000002256.

Abstract

We describe a female toddler with rectal bleeding from extensive colonic polyposis, and diagnosed with familial adenomatous polyposis. She has epilepsy from infancy attributed to focal cortical dysplasia. Hepatoblastoma was diagnosed at 13 months of age. Germline testing detected a pathogenic APC (adenomatous polyposis coli gene) variant. We discuss the anecdotal management of this case, including the clinical utility of genetic confirmation. We review the genotype-phenotype correlation of the APC mutational spectrum, and the existing evidence supporting the hypothesis that cortical dysplasia is part of the APC-related spectrum.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adenomatous Polyposis Coli Protein / genetics
  • Adenomatous Polyposis Coli* / complications
  • Adenomatous Polyposis Coli* / diagnosis
  • Adenomatous Polyposis Coli* / genetics
  • Female
  • Genes, APC
  • Genetic Association Studies
  • Germ-Line Mutation
  • Humans
  • Liver Neoplasms* / genetics
  • Malformations of Cortical Development* / genetics

Substances

  • Adenomatous Polyposis Coli Protein