Clinical manifestations in patients with hereditary nonpolyposis colorectal cancer

被引:0
作者
Tomoda, H
Baba, H
Oshiro, T
机构
[1] Dept. of Gastroenterological Surgery, National Kyushu Cancer Center, Fukuoka
[2] Dept. of Gastroenterological Surgery, National Kyushu Cancer Center, Minami-Ku, Fukuoka 815, 3-1-1, Notame
关键词
second primary cancer; HNPCC; colorectal cancer;
D O I
10.1002/(SICI)1096-9098(199604)61:4<262::AID-JSO5>3.0.CO;2-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The clinical manifestations of 1,042 Japanese patients with nonpolyposis colorectal cancer who underwent a resection between 1972 and 1992 at the National Kyushu Cancer Center were examined. Hereditary nonpolyposis colorectal cancer (HNPCC) was found in 39 (3.7%) patients. Some characteristic findings in HNPCC cases included early age of onset, a preponderance of right colon cancers, an increased frequency of colorectal cancers, and a favorable survival. Metachronous (postoperative) colorectal cancers developed significantly more often in cases with HNPCC than in those without (12.8% vs. 1.8%, P = 0.0001). Metachronous (postoperative) extracolonic cancers tended to develop more often in cases with HNPCC than in those without (10.2% vs. 3.5%, P = 0.053). In cases with HNPCC, the mean interval between the initial surgery and the diagnosis of the second cancer was 61 months (range; 12-153 months). These findings thus indicate the importance of routine and long-term follow-up to identify any second lesions, especially in patients with HNPCC. (C) 1996 Wiley-Liss, Inc.
引用
收藏
页码:262 / 266
页数:5
相关论文
共 27 条
[1]  
ALBANO WA, 1982, CANCER, V50, P360, DOI 10.1002/1097-0142(19820715)50:2<360::AID-CNCR2820500233>3.0.CO
[2]  
2-4
[3]  
CRISTOFARO G, 1987, CANCER, V60, P51, DOI 10.1002/1097-0142(19870701)60:1<51::AID-CNCR2820600110>3.0.CO
[4]  
2-V
[5]   FAMILIAL NON-POLYPOTIC CARCINOMA OF COLON [J].
FIELDING, JF .
BRITISH MEDICAL JOURNAL, 1969, 1 (5642) :512-&
[6]   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
[7]  
FREI JV, 1992, CANCER, V69, P1108
[8]   CONVENTION ON NOMENCLATURE FOR DNA CYTOMETRY [J].
HIDDEMANN, W ;
SCHUMANN, J ;
ANDREEFF, M ;
BARLOGIE, B ;
HERMAN, CJ ;
LEIF, RC ;
MAYALL, BH ;
MURPHY, RF ;
SANDBERG, AA .
CYTOMETRY, 1984, 5 (05) :445-446
[9]  
KOURI M, 1990, CANCER, V65, P1825, DOI 10.1002/1097-0142(19900415)65:8<1825::AID-CNCR2820650827>3.0.CO
[10]  
2-H