Prophylactic colectomy in patients with hereditary nonpolyposis colorectal cancer

被引:65
作者
Church, JM
机构
[1] David G. Jagelman Center for Inherited Colorectal Cancer, Department of Colorectal Surgery, Cleveland Clinic, Cleveland, OH
[2] Department of Colorectal Surgery, Cleveland Clinic Foundation, Cleveland, OH 44195
关键词
familial adenomatous polyposis; hereditary nonpolyposis colorectal cancer; prophylactic colectomy;
D O I
10.3109/07853899608999111
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Prophylactic colectomy is indicated in patients whose colons are at very high risk of developing cancer, Familial adenomatous polyposis (FAP) is the best example of a situation where prophylactic surgery is clearly necessary to prevent cancer, and has been shown to be effective in doing so, Recent advances in the molecular genetics of colorectal cancer have allowed presymptomatic diagnosis of patients with another dominantly inherited syndrome, hereditary nonpolyposis colorectal cancer (HNPCC), Prior to this, prophylactic colectomy had not been a consideration for patients in HNPCC families. A review of the outcome of colectomy and ileorectal anastomosis in FAP patients shows that although it is a major abdominal surgery there is a relatively low complication rate and the functional outcome is acceptable for a prophylactic procedure, The decision to apply colectomy to HNPCC patients depends on careful consideration of factors such as comorbidity, age, sphincter function, likely compliance with future surveillance and likely efficiency of colonoscopy as a cancer prevention strategy. In general, prophylactic colectomy is indicated in HNPCC gene carriers, because their lifetime risk for colorectal cancer is 80%.
引用
收藏
页码:479 / 482
页数:4
相关论文
共 15 条
[1]   FAMILIAL ADENOMATOUS POLYPOSIS - RESULTS FOLLOWING ILEAL POUCH-ANAL ANASTOMOSIS AND ILEORECTOSTOMY [J].
AMBROZE, WL ;
DOZOIS, RR ;
PEMBERTON, JH ;
BEART, RW ;
ILSTRUP, DM .
DISEASES OF THE COLON & RECTUM, 1992, 35 (01) :12-15
[2]  
CHURCH JM, IN PRESS DIS COLON R
[3]  
DECOSSE JJ, 1995, JNCI-J NATL CANCER I, V17, P31
[4]   RECOGNITION AND TREATMENT OF PATIENTS WITH HEREDITARY NONPOLYPOSIS COLON CANCER (LYNCH SYNDROME-I AND SYNDROME-II) [J].
FITZGIBBONS, RJ ;
LYNCH, HT ;
STANISLAV, GV ;
WATSON, PA ;
LANSPA, SJ ;
MARCUS, JN ;
SMYRK, T ;
KRIEGLER, MD ;
LYNCH, JF .
ANNALS OF SURGERY, 1987, 206 (03) :289-295
[5]   SCREENING REDUCES COLORECTAL-CANCER RATE IN FAMILIES WITH HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER [J].
JARVINEN, HJ ;
MECKLIN, JP ;
SISTONEN, P .
GASTROENTEROLOGY, 1995, 108 (05) :1405-1411
[6]  
JASS JR, 1994, ANTICANCER RES, V14, P1631
[7]  
LUDWIG K, IN PRESS DIS COLON R
[9]  
LYNCH HT, 1995, SEMIN COLON RECTAL S, V6, P38
[10]   COMPARISON OF MORBIDITY AND FUNCTION AFTER COLECTOMY WITH ILEORECTAL ANASTOMOSIS OR RESTORATIVE PROCTOCOLECTOMY FOR FAMILIAL ADENOMATOUS POLYPOSIS [J].
MADDEN, MV ;
NEALE, KF ;
NICHOLLS, RJ ;
LANDGREBE, JC ;
CHAPMAN, PD ;
BUSSEY, HJR ;
THOMSON, JPS .
BRITISH JOURNAL OF SURGERY, 1991, 78 (07) :789-792