Clinical and pathological analysis of 8 hereditary nonpolyposis colorectal cancer pedigrees.
- Author:
Yu WANG
1
;
Lei YANG
;
Yan-qing DING
;
Jing TONG
Author Information
- Publication Type:Journal Article
- MeSH: Adult; Aged; Colorectal Neoplasms, Hereditary Nonpolyposis; genetics; pathology; DNA Mismatch Repair; genetics; Female; Humans; Male; Middle Aged; Pedigree
- From: Journal of Southern Medical University 2009;29(12):2397-2400
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo analyze the clinical and pathological features of patients with hereditary nonpolyposis colorectal cancer (HNPCC).
METHODSThe data of 8 HNPCC pedigrees according with Amsterdam standard II were collected and their pedigree trees were generated.
RESULTSThe morbidity of HNPCC was 1.59%. Thirty-one patients were found in the 8 HNPCC pedigrees including 25 with colorectal cancer and 6 with extraintestinal tumors. The 8 probands consisted of 6 female and 2 male patients, among whom 4 were younger than 40 years old, 2 had lesions in the right colon, 3 in the left colon, and 3 in the rectum. The tumors were histologically identified mainly as highly to moderately differentiated adenocarcinoma; all the patients were free of lymph node or distant metastasis. Of the 8 probands, 5 had abnormal expression of MMR protein and only 1 had normal expression.
CONCLUSIONThe HNPCC probands are characterized by early onset at a young age and high differentiation of the tumor. The members of the pedigrees show a high incidence of the malignancies, and regular examination and timely treatment can be effective in preventing the tumor occurrence and reducing the mortality. Detection of MMR gene mutation can be a crucial approach to raising the diagnostic rate of HNPCC.