Delineating a new feature of constitutional mismatch repair deficiency (CMMRD) syndrome: breast cancer

Fam Cancer. 2019 Jan;18(1):105-108. doi: 10.1007/s10689-018-0088-0.

Abstract

Constitutional mismatch repair deficiency (CMMRD) syndrome is a rare autosomal recessive hereditary cancer condition, characterized by an exceptionally high risk of cancer, a propensity for childhood malignancies, and cutaneous features reminiscent of neurofibromatosis type 1 (NF1). We report on two sisters originally suspected of having CMMRD syndrome due to their history of colonic polyps and NF1 associated skin findings, both were subsequently found to have biallelic MSH6 mutations. After years of CMMRD syndrome follow-up, the proband was diagnosed with breast cancer at age 29, while her sister was diagnosed with a glioblastoma at age 27. Immunohistochemistry analysis on the breast tumor tissue revealed weak MSH6 protein staining. Exome sequencing revealed a hypermutated breast tumor and an ultra-hypermutated brain tumor. Multi-gene panel testing was also performed and revealed no additional mutations which might explain the proband's early onset breast cancer. This is the first documented case of breast cancer in an individual with CMMRD syndrome. We summarize the evidence supporting the possible association between breast cancer and biallelic MMR mutations. Healthcare providers should be aware of this possible association and follow-up appropriately for suspicious breast findings. In addition, this case highlights the need for frequent central nervous system screenings due to rapid progression of brain tumors.

Keywords: CMMRD; Constitutional mismatch repair deficiency syndrome; Hereditary brain tumor; Hereditary breast cancer; Lynch syndrome; MSH6.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Brain Neoplasms / genetics*
  • Breast Neoplasms / genetics*
  • Colorectal Neoplasms / genetics*
  • DNA-Binding Proteins / genetics*
  • Female
  • Genetic Testing
  • Humans
  • Mutation
  • Neoplastic Syndromes, Hereditary / genetics*
  • Pedigree
  • Young Adult

Substances

  • DNA-Binding Proteins
  • G-T mismatch-binding protein

Supplementary concepts

  • Turcot syndrome

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