首页> 美国卫生研究院文献>Bosnian Journal of Basic Medical Sciences >INCOMPLETE INTESTINAL METAPLASIA AS AN INDICATOR FOR EARLY DETECTION OF GASTRIC CARCINOMA IN THE EVENTS OF HELICOBACTER PYLORI POSITIVE CHRONIC ATROPHIC GASTRITIS
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INCOMPLETE INTESTINAL METAPLASIA AS AN INDICATOR FOR EARLY DETECTION OF GASTRIC CARCINOMA IN THE EVENTS OF HELICOBACTER PYLORI POSITIVE CHRONIC ATROPHIC GASTRITIS

机译:肠上皮不全为早期检测幽门螺杆菌阳性慢性萎缩性胃炎胃癌的指标

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摘要

The aim of the study was to ascertain the existence of intestinal metaplasia in gastric mucosa of patients with gastric carcinoma coupled with H. pylori positive chronic atrophic gastritis and possible connection of IM with the development of gastric carcinoma. The paper presents prospective study that included 50 patients with gastric carcinoma and 50 patients with chronic atrophic H. pylori positive gastritis. All the patients were subjected to gastroscopy as well as biopsy targeted at antrum, lesser curvature and corpus and at the area 1-2 cm removed from tumor lesion. Biopsy samples were sliced by microtome and stained. We analyzed presence, frequency and severity of inflammatory-regenerative, metaplastic and dysplastic changes in the mucosa and evaluated their prognostic value. We typed IM immunohistochemically. This study confirmed responsibility of H. pylori for inflammatory events in gastric mucosa in patients with gastric carcinoma. According to our findings incomplete IM of types IIa and IIb as precancerous lesion is responsible for the development of gastric carcinoma and is associated with chronic atrophic gastritis grade I and II (92% of subjects, p=0,0097, h=1, p=0,01). Thus, the finding of incomplete intestinal metaplasia may be used as an indicator for early gastric carcinoma detection. Patients with patho-histologicaly verified incomplete intestinal metaplasia associated with active chronic atrophic gastritis of levels I and II represent risk group for the development of gastric carcinoma of intestinal type.
机译:该研究的目的是确定胃癌合并幽门螺杆菌阳性的慢性萎缩性胃炎的患者胃黏膜中存在肠上皮化生以及IM与胃癌发展的可能联系。本文提出了一项前瞻性研究,包括50例胃癌患者和50例慢性萎缩性幽门螺杆菌阳性胃炎患者。所有患者均接受胃镜检查以及针对胃窦,小弯度和体以及从肿瘤病变处移出的1-2 cm区域的活检。通过切片机将活检样品切片并染色。我们分析了粘膜炎性再生,化生和发育异常改变的存在,频率和严重性,并评估了其预后价值。我们通过免疫组织化学方法输入了IM。这项研究证实了幽门螺杆菌对胃癌患者胃黏膜炎性事件的责任。根据我们的发现,由于癌前病变,IIa和IIb型IM的不完整是导致胃癌发展的原因,并且与I和II级慢性萎缩性胃炎有关(92%的受试者,p = 0,0097,h = 1,p = 0,01)。因此,发现不完全的肠上皮化生可以用作早期胃癌检测的指标。经病理组织学证实的肠上皮化生不全,伴有活跃的I级和II级慢性萎缩性胃炎的患者代表发生肠型胃癌的危险人群。

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