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活动性自身免疫性胃炎,无腺体完全萎缩

Active autoimmune gastritis without total atrophy of the glands.

作者信息

Stolte M, Baumann K, Bethke B, Ritter M, Lauer E, Eidt H

机构信息

Institut für Pathologie, Klinikum Bayreuth, Bundesrepublik Deutschland.

出版信息

Z Gastroenterol. 1992 Oct;30(10):729-35.

PMID:1441676
Abstract

To date, autoimmune gastritis has been diagnosed for the most part only when total atrophy of the oxyntic glands is detected. On the basis of 40 patients without total atrophy of the glands, and with parietal cell antibodies in the serum, we show that the diagnosis of type A gastritis is also possible in the pre-atrophic stage. The histological criteria for the diagnosis of active autoimmune gastritis without total atrophy of the glands are 1. usually dense, diffuse locally emphasized lymphocytic infiltration of the lamina propria between the glands in the oxyntic mucosa, 2. focal destruction of individual glands in the corpus of the stomach by lymphocytes, and 3. reactive pseudohypertrophy of the parietal cells. A comparison with a group of patients with autoimmune gastritis and total atrophy of the glands shows that in active autoimmune gastritis, too, women are more frequently affected than men (in both groups, the sex ratio is approximately 3:1). Patients without atrophy of the glands are, on average, about 12 years younger than those with "burnt out" type A gastritis (average age 69.98:57.80 years). While in the case of burnt out type A gastritis, no colonisation with Helicobacter pylori was to be found, such colonisation was demonstrated for the corpus mucosa in 22.5%, and for the antral mucosa in 15.0%. In 27.5% a minimal or low-grade inactive superficial gastritis, as may be seen after eradication of Helicobacter pylori, was additionally diagnosed in the antrum. A knowledge of the histological appearance of the pre-atrophic stage of type A gastritis might be of importance for the possible prevention of pernicious anaemia.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

迄今为止,自身免疫性胃炎大多仅在检测到胃体腺完全萎缩时才得以诊断。基于40例腺体未完全萎缩且血清中存在壁细胞抗体的患者,我们发现,在萎缩前期也可诊断出A型胃炎。诊断无腺体完全萎缩的活动性自身免疫性胃炎的组织学标准为:1. 通常致密、弥漫且局部强化的胃体黏膜腺体间固有层淋巴细胞浸润;2. 胃体部个别腺体被淋巴细胞局灶性破坏;3. 壁细胞反应性假肥大。与一组患有自身免疫性胃炎且腺体完全萎缩的患者相比,结果显示,在活动性自身免疫性胃炎中,女性受累也比男性更常见(两组的性别比均约为3:1)。腺体未萎缩的患者平均比患有“终末期”A型胃炎的患者年轻约12岁(平均年龄69.98岁比57.80岁)。在“终末期”A型胃炎病例中未发现幽门螺杆菌定植,但在胃体黏膜中发现22.5%有幽门螺杆菌定植,在胃窦黏膜中为15.0%。在27.5%的患者中,胃窦还额外诊断出根除幽门螺杆菌后可能出现的轻度或低度非活动性浅表性胃炎。了解A型胃炎萎缩前期的组织学表现可能对预防恶性贫血具有重要意义。(摘要截选于250词)

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