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遗传性非息肉病性结直肠癌相关的同步性早期结肠源性印戒细胞癌。一例黏膜内和一例黏膜下病例的形态学和免疫组化对比研究。

HNPCC-associated synchronous early-stage signet-ring cell carcinomas of colonic origin. A comparative morphological and immunohistochemical study of an intramucosal and a submucosal example.

作者信息

Klarskov Louise, Bernstein Inge, Holck Susanne

机构信息

Department of Pathology, HNPCC-register, Hvidovre Hospital, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.

出版信息

Virchows Arch. 2009 Jan;454(1):115-24. doi: 10.1007/s00428-008-0691-9. Epub 2008 Nov 11.

Abstract

Signet-ring cell carcinoma (SRCC) developing in the colorectum (CR) is infrequently identified at an early stage (no deeper than submucosa). Most such examples involve the submucosa. Merely 13 cases of intramucosal CR SRCC are at hand. We recently had the opportunity to study a specimen with two synchronous early-stage SRCC, developed in a 65-year-old hereditary nonpolyposis colorectal cancer male patient with a known disease-causing mutation in MLH1. A right hemicolectomy specimen comprised a 15-mm intramucosal cecal lesion, featuring zones of conventional tubular adenoma and intraepithelial SRCC as well as tumor cells multifocally permeating the lamina propria and a 12-mm submucosally expanding SRCC of the ascending colon. The intramucosal and intraepithelial as well as stromal lesional cells displayed a normal membranous expression of beta-catenin and E-cadherin; submucosally infiltrating cells featured alterations in this complex with loss of membranous expression of both proteins and a shift with nuclear accumulation of beta-catenin, suggesting a disruption of the Wingless signaling pathway taking place at the transition from the intramucosal to the submucosal level.

摘要

结直肠癌(CR)中发生的印戒细胞癌(SRCC)在早期(不超过黏膜下层)很少被发现。大多数此类病例累及黏膜下层。目前仅有13例黏膜内CR SRCC病例。我们最近有机会研究一份标本,该标本中有两例同时发生的早期SRCC,来自一名65岁的遗传性非息肉病性结直肠癌男性患者,其MLH1基因存在已知致病突变。右半结肠切除术标本包括一个15毫米的黏膜内盲肠病变,具有传统管状腺瘤区域和上皮内SRCC,以及肿瘤细胞多灶性浸润固有层,还有一个12毫米的升结肠黏膜下扩展型SRCC。黏膜内、上皮内以及间质病变细胞显示β-连环蛋白和E-钙黏蛋白呈正常膜表达;黏膜下浸润细胞在这一复合体中出现改变,两种蛋白的膜表达缺失,β-连环蛋白核内积聚,提示在从黏膜内到黏膜下水平的转变过程中Wingless信号通路发生了破坏。

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