Surveillance colonoscopy practice in Lynch syndrome in the Netherlands: A nationwide survey

被引：6

作者：

Koornstra, Jan J. ^{[1
]}

Vasen, Hans Fa

机构：

[1] Univ Groningen, Univ Med Ctr Groningen, Dept Gastroenterol & Hepatol, Groningen, Netherlands

[2] Leiden Univ Med Ctr, Dept Gastroenterol, Groningen, Netherlands

来源：

WORLD JOURNAL OF GASTROENTEROLOGY | 2007年 / 13卷 / 34期

关键词：

lynch syndrome; hereditary nonpolyposis; colorectal cancer; Colonoscopy; surveillance; chromoencloscopy;

D O I：

10.3748/wjg.v13.i34.4659

中图分类号：

R57 [消化系及腹部疾病];

学科分类号：

摘要：

Lynch syndrome, or hereditary nonpolyposis colorectal cancer (HNPCC), is the most common genetic disorder predisposing to colorectal cancer. As regular colonoscopic surveillance has been shown to reduce the incidence of colorectal cancer, this strategy is recommended worldwide. Recently, several advances in colonoscopic techniques have improved detection rates of neoplasia in Lynch syndrome. In this nationwide survey, we evaluated current surveillance colonoscopy practices for Lynch syndrome in the Netherlands and the extent to which advanced techniques have been adopted in routine clinical practice. (c) 2007 WJG. All rights reserved.

引用

页码：4658 / 4659

页数：2

共 11 条

[1] Surveillance for hereditary nonpolyposis colorectal cancer - A long-term study on 114 families [J].

Cappel, WHDTN ;

Nagengast, FM ;

Griffioen, G ;

Menko, FH ;

Taal, BG ;

Kleibeuker, JH ;

Vasen, HF .

DISEASES OF THE COLON & RECTUM, 2002, 45 (12) :1588-1594

[2] A prospective comparative study of narrow-band imaging, chromoendoscopy, and conventional colonoscopy in the diagnosis of colorectal neoplasia [J].

Chiu, Han-Mo ;

Chang, Chi-Yang ;

Chen, Chien-Chuan ;

Lee, Yi-Chia ;

Wu, Ming-Shiang ;

Lin, Jaw-Town ;

Shun, Chia-Tung ;

Wang, Hsiu-Po .

GUT, 2007, 56 (03) :373-379

[3] Decrease in mortality in Lynch syndrome families because of surveillance [J].

De Jong, AE ;

Hendriks, YMC ;

Kleibeuker, JH ;

De Boer, SY ;

Cats, A ;

Griffioen, G ;

Nagengast, FM ;

Nelis, FG ;

Rookus, MA ;

Vasen, HFA .

GASTROENTEROLOGY, 2006, 130 (03) :665-671

[4] Guidance on gastrointestinal surveillance for hereditary non-polyposis colorectal cancer, familial adenomatous polypolis, juvenile polyposis, and Peutz-Jeghers syndrome [J].

Dunlop, MG .

GUT, 2002, 51 :V21-V27

[5] The role of high-magnification-chromoscopic colonoscopy in hereditary nonpolyposis colorectal cancer screening: A prospective "back-to-back" endoscopic study [J].

Hurlstone, DP ;

Karajeh, M ;

Cross, SS ;

McAlindon, ME ;

Brown, S ;

Hunter, MD ;

Sanders, DS .

AMERICAN JOURNAL OF GASTROENTEROLOGY, 2005, 100 (10) :2167-2173

[6] Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer [J].

Järvinen, HJ ;

Aarnio, M ;

Mustonen, H ;

Aktan-Collan, K ;

Aaltonen, LA ;

Peltomäki, P ;

de la Chapelle, A ;

Mecklin, JP .

GASTROENTEROLOGY, 2000, 118 (05) :829-834

[7] Chromoendoscopic Colonoscopy for detecting preneoplastic lesions in hereditary nonpolyposis colorectal cancer syndrome [J].

Lecomte, T ;

Cellier, C ;

Meatchi, T ;

Barbier, JP ;

Cugnenc, PH ;

Jian, R ;

Laurent-Puig, P ;

Landi, B .

CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2005, 3 (09) :897-902

[8] Proximal adenomas in hereditary non-polyposis colorectal cancer are prone to rapid malignant transformation [J].

Rijcken, FEM ;

Hollema, H ;

Kleibeuker, JH .

GUT, 2002, 50 (03) :382-386

[9] Polyp miss rate determined by tandem colonoscopy: A systematic review [J].

van Rijn, JC ;

Reitsma, JB ;

Stoker, J ;

Bossuyt, PM ;

van Deventer, SJ ;

Dekker, E .

AMERICAN JOURNAL OF GASTROENTEROLOGY, 2006, 101 (02) :343-350

[10] Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer) [J].

Vasen, H. F. A. ;

Moslein, G. ;

Alonso, A. ;

Bernstein, I. ;

Bertario, L. ;

Blanco, I. ;

Burn, J. ;

Capella, G. ;

Engel, C. ;

Frayling, I. ;

Friedl, W. ;

Hes, F. J. ;

Hodgson, S. ;

Mecklin, J-P ;

Moller, P. ;

Nagengast, F. ;

Parc, Y. ;

Renkonen-Sinisalo, L. ;

Sampson, J. R. ;

Stormorken, A. ;

Wijnen, J. .

JOURNAL OF MEDICAL GENETICS, 2007, 44 (06) :353-362

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