Lynch syndrome type II associated endometrial carcinoma: a case report
and literature analysis
Lynch syndrome (LS) is an autosomal dominant hereditary disease, which
is caused by mismatch repair (MMR) gene mutations in the germline of
MLH1, MSH2, MSH6 and PMS2. LS patients can develop colorectal cancer,
endometrial cancer (EC), etc, at the same or different time, so their
prognosis are poor.