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直肠保留手术可能适用于双等位基因突变 MutYH 相关息肉病。

Rectum-sparing surgery may be appropriate for biallelic MutYH-associated polyposis.

机构信息

Department of Medical and Surgical Sciences, University of Brescia, Brescia, Italy.

出版信息

Dis Colon Rectum. 2010 Dec;53(12):1670-5. doi: 10.1007/DCR.0b013e3181ee3d6b.

Abstract

PURPOSE

The risk of cancer or severe polyposis of the rectal stump after total colectomy for MutYH-associated polyposis is scarcely defined. To evaluate this risk, we describe the findings of endoscopic surveillance of the rectal stump in a series of patients with biallelic MutYH mutations and polyposis.

METHODS

This is a retrospective, observational, multicenter case series derived from 2 familial cancer registries. Biallelic, germ-line MutYH mutations were found in 14 patients with no adenomatous polyposis coli gene mutations. Eleven of them underwent total colectomy with ileorectal anastomosis and yearly proctoscopic surveillance thereafter. Phenotype and histology of rectal polyps were recorded at diagnosis and during follow-up. Development of adenomas and carcinomas during endoscopic surveillance of the rectal stump was observed.

RESULTS

At diagnosis, 6 patients had attenuated polyposis (10-100 adenomas), 5 patients had classical polyposis, 8 patients had colon carcinoma, and no patient had rectal carcinoma. The mean number of rectal polyps at diagnosis was 2.64 ± 2.11 (range, 0-6). No patients had rectal cancer. The most frequent MutYH mutations were Y165C/Y165C and G382D/G382D in 6 and 2 patients, respectively. During surveillance of the rectal stump after surgery (median duration, 5 y; range, 2-23 y), no patient developed rectal cancer. The mean number of adenomas per proctoscopy was 1.23 ± 2.19 (range, 0-10 adenomas per proctoscopy). This study was limited by the small size and retrospective nature of the case series.

CONCLUSION

Total colectomy with ileorectal anastomosis may be appropriate for patients with MutYH-associated polyposis, provided that they have no rectal cancer or severe rectal polyposis at presentation and that they undergo yearly endoscopic surveillance thereafter.

摘要

目的

全结肠切除术后,由于 MutYH 相关息肉病导致直肠残端发生癌症或严重息肉病的风险尚不清楚。为了评估这种风险,我们描述了一系列双等位 MutYH 突变和息肉病患者直肠残端内镜监测的结果。

方法

这是一项来自 2 个家族性癌症登记处的回顾性、观察性、多中心病例系列研究。在 14 名无腺瘤性结肠息肉病基因突变的患者中发现了双等位、种系 MutYH 突变。其中 11 人接受了全结肠切除术和回肠直肠吻合术,此后每年进行直肠内窥镜监测。在诊断时和随访期间记录直肠息肉的表型和组织学。观察直肠残端内镜监测期间腺瘤和癌的发展情况。

结果

诊断时,6 例患者有轻度息肉病(10-100 个腺瘤),5 例患者有经典息肉病,8 例患者有结肠癌,无患者有直肠癌。诊断时直肠息肉的平均数量为 2.64±2.11(范围,0-6)。无患者患有直肠癌。最常见的 MutYH 突变是 Y165C/Y165C 和 G382D/G382D,分别在 6 例和 2 例患者中发现。手术后直肠残端监测期间(中位随访时间 5 年;范围,2-23 年),无患者发生直肠癌。每次直肠镜检查的平均腺瘤数量为 1.23±2.19(范围,每次直肠镜检查 0-10 个腺瘤)。本研究受到病例系列小样本量和回顾性的限制。

结论

对于无直肠癌或严重直肠息肉病且术后每年接受内镜监测的 MutYH 相关息肉病患者,全结肠切除术和回肠直肠吻合术可能是合适的选择。

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