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胃窦和胃体小肠化生发展过程中的组织病理学差异。

Histopathological differences in the development of small intestinal metaplasia between antrum and body of stomach.

作者信息

Ikeda Yoshiyuki, Nishikura Ken, Watanabe Hidenobu, Watanabe Gen, Ajioka Yoichi, Hatakeyama Katsuyoshi

机构信息

Division of Molecular and Diagnostic Pathology, Department of Molecular Genetics, Niigata University Graduate School of Medical and Dental Science, Niigata, Japan.

出版信息

Pathol Res Pract. 2005;201(7):487-96. doi: 10.1016/j.prp.2005.05.008.

Abstract

This study used mucin immunohistochemistry to investigate differences in the properties of intestinal metaplasia between the antrum and body of the stomach in 28 resected specimens. Intestinal metaplasia was classified as: (1) small intestinal metaplasia (SIM) with a tubule, including CD10-positive brush border on a background of MUC5AC-/ HGM-negative cells; or (2) goblet cell metaplasia (GCM) with MUC2-positive and CD10-negative cells. In the antrum, frequencies of SIM and GCM were nearly equal irrespective of metaplasia grade. Frequency and length of remnant pyloric gland for SIM were significantly greater in the antrum than in the body. In the proliferative zone, there existed a lower level in SIM than in non-intestinalized tubules. These findings suggest that the proliferative zone shifts from the neck zone toward the bottom of the tubule during the SIM process in the antrum. In the body, however, the grade of SIM grade was significantly higher than that of GCM. The proliferative zone was located higher in the fundic gland, pseudopyloric gland and SIM, in that order. Almost all remnant pyloric glands for SIM were negative for pepsinogen I. These facts indicate that SIM in the body originates in a proliferative zone that shifted downward to an area near the bottom of the tubule, with atrophic pyloric glands originating from pseudopyloric gland metaplasia.

摘要

本研究采用黏蛋白免疫组织化学方法,对28例切除标本胃窦和胃体肠化生的特性差异进行了研究。肠化生分为:(1)小肠化生(SIM),呈小管状,在MUC5AC-/HGM阴性细胞背景下有CD10阳性刷状缘;或(2)杯状细胞化生(GCM),有MUC2阳性和CD10阴性细胞。在胃窦,无论化生程度如何,SIM和GCM的发生率几乎相等。胃窦中SIM的残余幽门腺频率和长度显著高于胃体。在增殖区,SIM中的水平低于非肠化生的小管。这些发现表明,在胃窦的SIM过程中,增殖区从颈部向小管底部移动。然而,在胃体中,SIM的程度显著高于GCM。增殖区依次位于胃底腺、假幽门腺和SIM的较高位置。几乎所有SIM的残余幽门腺胃蛋白酶原I均为阴性。这些事实表明,胃体中的SIM起源于向下移动到小管底部附近区域的增殖区,萎缩性幽门腺起源于假幽门腺化生。

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