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比较六种免疫组织化学标志物在 Barrett 食管肿瘤组织学诊断中的应用。

Comparison of six immunohistochemical markers for the histologic diagnosis of neoplasia in Barrett's esophagus.

机构信息

Institute for Laboratory Medicine and Pathobiochemistry, Charité-University Medical Center, Berlin, Germany.

出版信息

Virchows Arch. 2010 Nov;457(5):537-45. doi: 10.1007/s00428-010-0972-y. Epub 2010 Sep 16.

Abstract

In esophageal neoplasms, the histopathologic differentiation between Barrett's esophagus with or without intraepithelial neoplasia and adenocarcinoma is often challenging. Immunohistochemistry might help to differentiate between these lesions. The expression of CDX2, LI-cadherin, mucin 2 (MUC2), blood group 8 (BG8, Lewis(y)), claudin-2, and villin was investigated in normal gastroesophageal (n = 23) and in Barrett's (n = 17) mucosa, in low-grade (n = 12) and high-grade (n = 9) intraepithelial neoplasia (IEN) as well as in esophageal adenocarcinoma (n = 16), using immunohistochemistry. For CDX2 and LI-cadherin, the immunoreactivity score was highest in IEN while for MUC2, BG8, and villin, it dropped gradually from Barrett's via IEN to adenocarcinoma, and expression of Claudin-2 was only weak and focal in all lesions. The expression of MUC2 and LI-cadherin differed significantly between all examined lesions except between low-grade and high-grade IEN. MUC2 and LI-cadherin are useful immunohistochemical markers for the differentiation between normal glandular mucosa, Barrett's mucosa, IEN, and invasive carcinoma of the esophagus; however, none of the examined markers was helpful for the differentiation between low-grade and high-grade IEN.

摘要

在食管肿瘤中,巴雷特食管伴或不伴上皮内瘤变与腺癌的组织病理学鉴别常常具有挑战性。免疫组织化学可能有助于区分这些病变。本研究应用免疫组织化学方法检测了正常胃食管(n=23)和巴雷特(n=17)黏膜、低级别上皮内瘤变(n=12)和高级别上皮内瘤变(n=9)以及食管腺癌(n=16)中 CDX2、LI-钙黏蛋白、黏蛋白 2(MUC2)、血型抗原 8(BG8,Lewis(y))、claudin-2 和微管相关蛋白 2(villin)的表达情况。对于 CDX2 和 LI-钙黏蛋白,免疫反应评分在 IEN 中最高,而对于 MUC2、BG8 和 villin,则从巴雷特依次递降到腺癌,claudin-2 的表达在所有病变中均较弱且局限。MUC2 和 LI-钙黏蛋白在除低级别和高级别 IEN 之外的所有检查病变之间的表达差异有统计学意义。MUC2 和 LI-钙黏蛋白是区分正常腺黏膜、巴雷特黏膜、IEN 和食管浸润性癌的有用免疫组织化学标志物;然而,检查的标志物均无助于区分低级别和高级别 IEN。

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