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在遗传性非息肉病性结直肠癌筛查中,染色结肠镜检查比白光结肠镜检查或窄带成像结肠镜检查能检测出更多的腺瘤。

Chromocolonoscopy detects more adenomas than white light colonoscopy or narrow band imaging colonoscopy in hereditary nonpolyposis colorectal cancer screening.

作者信息

Hüneburg R, Lammert F, Rabe C, Rahner N, Kahl P, Büttner R, Propping P, Sauerbruch T, Lamberti C

机构信息

Department of Internal Medicine I, University of Bonn, Germany.

出版信息

Endoscopy. 2009 Apr;41(4):316-22. doi: 10.1055/s-0028-1119628. Epub 2009 Apr 1.

Abstract

BACKGROUND AND STUDY AIMS

Individuals carrying germline mutations in one of the genes responsible for hereditary nonpolyposis colon cancer (HNPCC) have a lifetime risk of up to 80 % of developing colorectal cancer. As there is evidence for a higher incidence of flat adenomatous precursors and because an accelerated adenoma-carcinoma sequence has been postulated for these patients, early detection of these lesions is essential. It was the aim of the present study to assess the detection rate of polypoid lesions by comparing chromocolonoscopy with standard white light colonoscopy and narrow-band imaging (NBI) colonoscopy.

PATIENTS AND METHODS

109 patients were included (98 with a functionally relevant mutation in a mismatch repair gene, 11 fulfilling the strict Amsterdam criteria). In 47 patients, standard colonoscopy was followed by chromocolonoscopy with indigo carmine. In 62 patients, NBI was performed first followed by chromocolonoscopy.

RESULTS

A total of 128 hyperplastic and 52 adenomatous lesions were detected. In the first series, 0.5 lesions/patient were identified by standard colonoscopy and 1.5 lesions/patient by chromocolonoscopy ( P < 0.001). In the second series, 0.7 lesions/patient were detected by NBI colonoscopy and 1.8 lesions/patient by chromocolonoscopy ( P = 0.01). At least one adenoma was detected in 15 % of patients by both standard and NBI colonoscopy compared with 28 % of patients by chromocolonoscopy.

CONCLUSION

According to this study, chromocolonoscopy detects significantly more hyperplastic and, in particular, adenomatous lesions than standard white light colonoscopy or NBI.

摘要

背景与研究目的

携带遗传性非息肉病性结直肠癌(HNPCC)相关基因之一种系突变的个体,患结直肠癌的终生风险高达80%。由于有证据表明扁平腺瘤性前驱病变的发病率较高,且假定这些患者存在腺瘤 - 癌序列加速现象,因此早期检测这些病变至关重要。本研究的目的是通过比较染色结肠镜检查与标准白光结肠镜检查和窄带成像(NBI)结肠镜检查来评估息肉样病变的检出率。

患者与方法

纳入109例患者(98例错配修复基因存在功能相关突变,11例符合严格的阿姆斯特丹标准)。47例患者先进行标准结肠镜检查,随后进行靛胭脂染色结肠镜检查。62例患者先进行NBI检查,随后进行染色结肠镜检查。

结果

共检测到128个增生性病变和52个腺瘤性病变。在第一组中,标准结肠镜检查平均每位患者发现0.5个病变,染色结肠镜检查平均每位患者发现1.5个病变(P < 0.001)。在第二组中,NBI结肠镜检查平均每位患者发现0.7个病变,染色结肠镜检查平均每位患者发现1.8个病变(P = 0.01)。标准结肠镜检查和NBI结肠镜检查分别在15%的患者中检测到至少一个腺瘤,而染色结肠镜检查在28%的患者中检测到至少一个腺瘤。

结论

根据本研究,与标准白光结肠镜检查或NBI相比,染色结肠镜检查能显著检测到更多的增生性病变,尤其是腺瘤性病变。

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