[Recognising hereditary non-polyposis colorectal cancer without a clear family history]

Ned Tijdschr Geneeskd. 2004 Oct 16;148(42):2053-7.
[Article in Dutch]

Abstract

In 3 patients, 2 men aged 46 and 51 years and a woman aged 54 years, with colorectal cancer there was insufficient information on the basis of the family history to diagnose 'hereditary non-polyposis colorectal cancer' (HNPCC). Further investigation showed microsatellite instability in the tumour material, an indicator for a mutation in DNA-'mismatch repair' (MMR-) genes. Immunohistochemical study of lymphocytes showed an absence of the gene products MSH2 and MSH6. Study of the MMR genes revealed a pathogenic germ-line mutation in MSH2. All three patients were satisfied with genetic testing of the MMR-genes as this gave their children and their family members the opportunity to clarify genetic status. HNPCC is a clinical diagnosis, based on family history. As family history taking is often incomplete, the diagnosis is regularly not considered. The following individual criteria can help to recognize a patient at risk for HNPCC: (a) colorectal cancer diagnosed below 50 years of age, (b) second colorectal cancer, (c) a combination of colorectal and endometrial cancer.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Base Pair Mismatch / genetics
  • Colorectal Neoplasms, Hereditary Nonpolyposis / diagnosis
  • Colorectal Neoplasms, Hereditary Nonpolyposis / genetics*
  • DNA Mutational Analysis
  • DNA Repair / genetics
  • DNA-Binding Proteins / genetics*
  • Female
  • Germ-Line Mutation*
  • Humans
  • Male
  • Middle Aged
  • MutS Homolog 2 Protein
  • Netherlands
  • Pedigree
  • Proto-Oncogene Proteins / genetics*

Substances

  • DNA-Binding Proteins
  • G-T mismatch-binding protein
  • Proto-Oncogene Proteins
  • MSH2 protein, human
  • MutS Homolog 2 Protein