Definition

  • Phenotypic variant of HNPCC
    • Germaine mutation in MLH1, MSH2, MSH6, and PMS2
  • Approximately one-third of cases of Muir-Torre syndrome are caused by MUTYH variants and may represent a clinical phenotype of MUTYH-associated polyposis, an autosomal recessive polyposis syndrome caused by biallelic pathogenic variants in the base excision repair gene MUTYH.

Clinical

  • Sebaceous cutaneous neoplasms
    • Sebaceous adenomas
    • sebaceous epitheliomas
    • sebaceous carcinomas
    • keratoacanthomas
  • Visceral neoplasms
    • Colorectal
    • Breast
    • Endometrial
    • Ovarian
    • Urothelial cancers