Hebbard P C, Macmillan A, Huntsman D, Kaurah P, Carneiro F, Wen X, Kwan A, Boone D, Bursey F, Green J, Fernandez B, Fontaine D, Wirtzfeld D A
Department of Surgery, Memorial University, St John's, NL, Canada.
Ann Surg Oncol. 2009 Jul;16(7):1890-5. doi: 10.1245/s10434-009-0471-z. Epub 2009 May 1.
BACKGROUND: Hereditary diffuse gastric cancer (HDGC) results from truncating mutations of the CDH1 (E-cadherin) gene. It is an autosomal dominant cancer susceptibility syndrome with a lifetime risk of diffuse gastric cancer (DGC) of 60-80%, with a mean age of onset of 37 years. There exists no adequate screening test for DGC. Early intramucosal diffuse/signet-ring cell carcinomas have been found in prophylactic total gastrectomy (PTG) specimens following normal preoperative endoscopy. Total gastrectomy has been advocated on a prophylactic basis. The aim of this study was to report our experience with PTG in 23 patients from the Canadian province of Newfoundland and Labrador. This is the largest series worldwide. METHODS: A retrospective study of consecutive patients undergoing PTG for HDGC was performed. All patients were confirmed to have a truncating mutation of the CDH1 gene. RESULTS: Twenty-three patients underwent PTG between February 2006 and November 2008. Major complications were found in 4/23 patients (17%), with no mortality. Two of 23 patients (9%) had positive mucosal biopsies on preoperative EGD. Twenty-two of 23 patients (96%) had evidence of diffuse/signet-ring carcinoma on final standardized pathological evaluation. Therefore, 21/23 (91%) were not picked up by preoperative EGD screening. CONCLUSIONS: PTG can be performed in patients with HDGC with a low rate of serious complications. Methods of reconstruction incorporating a pouch reservoir and preservation of the postgastric branches of the vagus nerves need to be explored. More refined penetrance estimates, effective screening protocols, and long-term psychological and functional outcomes following PTG require organized multicenter collaborative efforts.
背景:遗传性弥漫性胃癌(HDGC)由CDH1(E-钙黏蛋白)基因的截短突变引起。它是一种常染色体显性癌症易感综合征,终生患弥漫性胃癌(DGC)的风险为60 - 80%,平均发病年龄为37岁。目前尚无针对DGC的充分筛查试验。在术前内镜检查正常的情况下,预防性全胃切除术(PTG)标本中发现了早期黏膜内弥漫性/印戒细胞癌。预防性全胃切除术已被提倡。本研究的目的是报告我们在加拿大纽芬兰和拉布拉多省对23例患者进行PTG的经验。这是全球最大的系列研究。 方法:对连续接受PTG治疗HDGC的患者进行回顾性研究。所有患者均被证实存在CDH1基因的截短突变。 结果:2006年2月至2008年11月期间,23例患者接受了PTG。4/23例患者(17%)出现主要并发症,无死亡病例。23例患者中有2例(9%)术前上消化道内镜检查黏膜活检呈阳性。23例患者中有22例(96%)在最终标准化病理评估中有弥漫性/印戒癌证据。因此,21/23例(91%)未被术前内镜筛查检出。 结论:HDGC患者可进行PTG,严重并发症发生率较低。需要探索结合袋状贮器重建和保留迷走神经胃后支的方法。更精确的外显率估计、有效的筛查方案以及PTG后的长期心理和功能结果需要有组织的多中心协作努力。
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