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对可能伴有癌变的壶腹绒毛状腺瘤的治疗。

Treatment of ampullary villous adenomas that may harbor carcinoma.

作者信息

Jordan Paul H, Ayala Gustavo, Rosenberg Wade R, Kinner Beatriz M

机构信息

Department of Surgery, Baylor College of Medicine, Houston, Texas, USA.

出版信息

J Gastrointest Surg. 2002 Sep-Oct;6(5):770-5. doi: 10.1016/s1091-255x(02)00040-9.

Abstract

Villous adenoma of the ampulla of Vater is a rare tumor. It is a deceptive tumor because it is a premalignant lesion and biopsies of the lesion are false negative in 25% to 56% of patients. The primary focus of this report is 23 of 30 patients with villous adenoma of the ampulla of Vater who underwent Whipple operations. Paraffin blocks from 22 patients were available. In eight patients, blocks of the biopsies and the corresponding resected specimens were available. Immunohistochemical studies using antibodies to p53 and Ki-67 were performed to determine whether accumulation of these antibodies in the biopsy specimens would identify false negative biopsies. There was one operative death. The 2-, 5-, and 10-year survival rates for the 22 patients surviving a Whipple operation were 74%, 57%, and 35%, respectively. Three patients died of cancer. The mean p53 expression index was increased in adenomas to 88 (P = 0.001) and in carcinomas to 114 (P = 0.01), compared with 12.6 for normal ampullary epithelium adjacent to tumor. Significant differences in the Ki-67 proliferation index were noted between normal adjacent epithelium (13%), adenoma (34%, P = 0.0002), and carcinoma (53%, P = 0.034), as well as between adenomatous epithelium and carcinoma (34% vs. 53%, P = .012). Villous ampullary adenocarcinoma was present in 65% of patients with villous adenoma (87% if patients with carcinoma in situ in resected specimens are included). Because of the high false negative rate of ampullary biopsies, and the inability to accurately stage these lesions, we recommend pancreaticoduodenectomy in most patients. Studies with p53 and Ki-67 markers suggest that they may be helpful in the recognition of ampullary villous cancer not identified on routine biopsies.

摘要

Vater壶腹绒毛状腺瘤是一种罕见的肿瘤。它是一种具有欺骗性的肿瘤,因为它是一种癌前病变,在25%至56%的患者中,该病变的活检结果为假阴性。本报告的主要研究对象是30例接受了Whipple手术的Vater壶腹绒毛状腺瘤患者中的23例。有22例患者的石蜡块可供使用。在8例患者中,活检组织块和相应的切除标本均可供使用。使用抗p53和Ki-67抗体进行免疫组织化学研究,以确定这些抗体在活检标本中的积累是否能识别出假阴性活检。有1例手术死亡。22例接受Whipple手术后存活的患者,其2年、5年和10年生存率分别为74%、57%和35%。3例患者死于癌症。与肿瘤旁正常壶腹上皮的12.6相比,腺瘤中的平均p53表达指数增加到88(P = 0.001),癌中的平均p53表达指数增加到114(P = 0.01)。在正常相邻上皮(13%)、腺瘤(34%,P = 0.0002)和癌(53%,P = 0.034)之间,以及腺瘤上皮和癌之间(34%对53%,P = 0.012),Ki-67增殖指数存在显著差异。绒毛状壶腹腺癌在绒毛状腺瘤患者中占65%(如果包括切除标本中有原位癌的患者,则为87%)。由于壶腹活检的假阴性率高,且无法准确分期这些病变,我们建议大多数患者行胰十二指肠切除术。对p53和Ki-67标志物的研究表明,它们可能有助于识别常规活检未发现的壶腹绒毛状癌。

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