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食管发育异常与腺癌:一项针对肠型和胃型标志物的双重免疫染色研究

Esophageal dysplasia and adenocarcinoma: a study with double immunostaining for intestinal and gastric markers.

作者信息

Chlumská Alena, Mukenšnabl Petr, Waloschek Tomáš, Zámečník Michal

出版信息

Cesk Patol. 2018 Summer;54(2):81-85.

Abstract

Columnar lined esophagus is a complication of long term gastroesophageal reflux disease and the main precursor of esophageal adenocarcinoma. Incomplete intestinal metaplasia in reflux esophagitis represents one of the most important risk factors for neoplastic transformation through the metaplasia-dysplasia-adenocarcinoma sequence. However, recent studies suggest that cardiac type mucosa also shows molecular abnormalities which are similar to those of incomplete intestinal metaplasia. Immunohistochemically, three types of esophageal dysplasia and adenocarcinoma are recognized: adenomatous-intestinal, hybrid/mixed and foveolar gastric types. We are interested in the phenotypes of these dysplasias and adenocarcinomas, especially in the possible relationship between them. For this reason, we evaluated the immunohistochemical expression of intestinal and gastric markers in a series of 30 cases of esophageal high-grade dysplasia (high-grade intraepithelial neoplasia) and of 70 adenocarcinomas. For immunohistochemical classification, we used double immunohistochemical reactions CDX2/MUC5AC and CDX2/MUC6, respectively. In cases of incomplete intestinal metaplasia, hybrid/mixed high-grade dysplasia and hybrid/mixed adenocarcinoma, we found the expression of gastric mucins MUC5AC and MUC6 only in cells with intestinal differentiation (with nuclear positivity for CDX2). The double immunostaining excluded the presence of the cells with "pure" foveolar gastric phenotype in hybrid lesions. Thus, the hybrid category actually represents the intestinal type dysplasia/adenocarcinoma (which is known to have a better prognosis than the foveolar gastric type). Keywords: immunohistochemistry - double immunostaining - reflux esophagitis - Barrett esophagus - esophageal dysplasia - esophageal adenocarcinoma.

摘要

柱状上皮化生食管是长期胃食管反流病的并发症,也是食管腺癌的主要前驱病变。反流性食管炎中的不完全肠化生是通过化生-发育异常-腺癌序列发生肿瘤转化的最重要危险因素之一。然而,最近的研究表明,贲门型黏膜也表现出与不完全肠化生相似的分子异常。免疫组织化学上,可识别出三种类型的食管发育异常和腺癌:腺瘤性肠型、混合型和胃小凹型。我们对这些发育异常和腺癌的表型感兴趣,尤其是它们之间可能存在的关系。因此,我们评估了30例食管高级别发育异常(高级别上皮内瘤变)和70例腺癌中肠和胃标志物的免疫组织化学表达。对于免疫组织化学分类,我们分别使用了双重免疫组织化学反应CDX2/MUC5AC和CDX2/MUC6。在不完全肠化生、混合型高级别发育异常和混合型腺癌病例中,我们发现胃黏液蛋白MUC5AC和MUC6仅在具有肠化生的细胞中表达(CDX2核阳性)。双重免疫染色排除了混合性病变中存在“纯”胃小凹型细胞的情况。因此,混合型实际上代表肠型发育异常/腺癌(已知其预后比胃小凹型好)。关键词:免疫组织化学-双重免疫染色-反流性食管炎-巴雷特食管-食管发育异常-食管腺癌

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