Chromoendoscopic colonoscopy for detecting preneoplastic lesions in hereditary nonpolyposis colorectal cancer syndrome
- PMID: 16234028
- DOI: 10.1016/s1542-3565(05)00403-9
Chromoendoscopic colonoscopy for detecting preneoplastic lesions in hereditary nonpolyposis colorectal cancer syndrome
Abstract
Background & aims: In hereditary nonpolyposis colorectal cancer (HNPCC) syndrome, flat and small adenomas are particularly prone to malignant transformation but might be missed by standard colonoscopy. We prospectively studied the diagnostic yield of high-resolution colonoscopy coupled with chromoendoscopy for preneoplastic and neoplastic colorectal lesions in patients with HNPCC syndrome.
Methods: Thirty-six consecutive asymptomatic patients (mean age, 42 years) belonging to HNPCC families and receiving genetic counseling were enrolled in this prospective study. Colonoscopy was performed in 2 steps. Conventional colonoscopy was performed first, followed by a second colonoscopy with chromoendoscopy with indigo carmine (.4%) dye sprayed onto the entire proximal colon.
Results: Conventional colonoscopy identified 25 lesions (mean size, 4 +/- 3 mm) in 13 patients. Seven lesions, detected in 5 patients, were adenomas, 3 of which were located in the proximal colon. Chromoendoscopy identified additional 45 lesions (mean size, 3 +/- 1 mm) in 20 patients; most of these lesions were flat and hyperplastic. Eleven additional adenomas were detected in the proximal colon of 8 patients, and 8 of these 11 lesions were flat. The use of chromoendoscopy significantly increased the detection rate of adenomas in the proximal colon, from 3 of 33 patients to 10 of 33 patients (P = .045).
Conclusion: Relative to conventional colonoscopy, high-resolution colonoscopy with chromoendoscopy markedly improves the detection of adenomas in patients with HNPCC syndrome and might help to prevent colorectal carcinoma in these patients with a very high risk of colorectal cancer.
Similar articles
-
Chromocolonoscopy detects more adenomas than white light colonoscopy or narrow band imaging colonoscopy in hereditary nonpolyposis colorectal cancer screening.Endoscopy. 2009 Apr;41(4):316-22. doi: 10.1055/s-0028-1119628. Epub 2009 Apr 1. Endoscopy. 2009. PMID: 19340735
-
Missed adenomas during colonoscopic surveillance in individuals with Lynch Syndrome (hereditary nonpolyposis colorectal cancer).Cancer Prev Res (Phila). 2008 Nov;1(6):470-5. doi: 10.1158/1940-6207.CAPR-08-0098. Cancer Prev Res (Phila). 2008. PMID: 19138994 Free PMC article. Clinical Trial.
-
Magnetic resonance colonography for colorectal cancer screening in patients with Lynch syndrome gene mutation.Fam Cancer. 2010 Dec;9(4):555-61. doi: 10.1007/s10689-010-9350-9. Fam Cancer. 2010. PMID: 20495877
-
[Current concepts in the genetics of hereditary and sporadic colorectal cancer and the role of genetics in patient management. Hereditary colorectal cancers].Orv Hetil. 2006 Feb 26;147(8):363-8. Orv Hetil. 2006. PMID: 16579336 Review. Hungarian.
-
Hereditary nonpolyposis colorectal cancer (Lynch syndrome): criteria for identification and management.Dig Dis Sci. 2005 Feb;50(2):336-44. doi: 10.1007/s10620-005-1607-z. Dig Dis Sci. 2005. PMID: 15745097 Review.
Cited by
-
Colon cancer screening with image-enhanced endoscopy.Clin Endosc. 2014 Nov;47(6):504-8. doi: 10.5946/ce.2014.47.6.504. Epub 2014 Nov 30. Clin Endosc. 2014. PMID: 25505715 Free PMC article. Review.
-
Chromoendoscopy detects more adenomas than colonoscopy using intensive inspection without dye spraying.Cancer Prev Res (Phila). 2008 Dec;1(7):507-13. doi: 10.1158/1940-6207.CAPR-08-0096. Cancer Prev Res (Phila). 2008. PMID: 19139000 Free PMC article. Clinical Trial.
-
Diagnosis and management of hereditary colorectal cancer syndromes: Lynch syndrome as a model.CMAJ. 2009 Sep 1;181(5):273-80. doi: 10.1503/cmaj.071574. Epub 2009 Aug 4. CMAJ. 2009. PMID: 19654196 Free PMC article. Review. No abstract available.
-
From Genetics to Histomolecular Characterization: An Insight into Colorectal Carcinogenesis in Lynch Syndrome.Int J Mol Sci. 2021 Jun 23;22(13):6767. doi: 10.3390/ijms22136767. Int J Mol Sci. 2021. PMID: 34201893 Free PMC article. Review.
-
Phenotypic and genotypic heterogeneity of Lynch syndrome: a complex diagnostic challenge.Fam Cancer. 2018 Jul;17(3):403-414. doi: 10.1007/s10689-017-0053-3. Fam Cancer. 2018. PMID: 29071502 Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical