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胃类癌及其前驱病变。23例的组织学和免疫组化研究。

Gastric carcinoids and their precursor lesions. A histologic and immunohistochemical study of 23 cases.

作者信息

Bordi C, Yu J Y, Baggi M T, Davoli C, Pilato F P, Baruzzi G, Gardini G, Zamboni G, Franzin G, Papotti M

机构信息

Institute of Pathological Anatomy, University of Parma, Italy.

出版信息

Cancer. 1991 Feb 1;67(3):663-72. doi: 10.1002/1097-0142(19910201)67:3<663::aid-cncr2820670323>3.0.co;2-l.

Abstract

A histologic and immunohistochemical study was carried out in 23 unselected nonantral gastric carcinoids and their precursor lesions classified according to Solcia et al. None of the patients showed Zollinger-Ellison syndrome. Two variants of carcinoids showing distinctive pathologic and pathogenetic characteristics were identified on the basis of presence or absence of associated chronic atrophic gastritis type A (A-CAG). Chronic atrophic gastritis type A was found in 19 cases showing either single or multiple neoplasms, tumor extension limited to the mucosa or submucosa, consistent endocrine cell precursor changes in extratumoral mucosa, and consistent hypergastrinemia and/or G cell hyperplasia. Associated precursor lesions were only hyperplastic in all but two cases with single carcinoids whereas they were also dysplastic in all but one case with multiple carcinoids. The four tumors arising in nonatrophic mucosa were all single, more aggressive, and not associated with extratumoral endocrine cell proliferations or with signs of gastrin hypersecretion. Tumor cells were diffusely immunoreactive for chromogranin A and synaptophysin but usually negative for chromogranin B or HISL-19. Scattered serotonin cells were found in ten carcinoids. They were more frequent in infiltrating than in intramucosal tumors as were the less represented pancreatic polypeptide cells whereas the reverse was found for alpha-subunit-containing cells. These results are of relevance for tumor pathogenesis and may provide the rationale for a less aggressive therapeutic approach in the patients.

摘要

对23例未经选择的非胃窦部胃类癌及其根据索尔恰等人分类的前驱病变进行了组织学和免疫组织化学研究。所有患者均未表现出卓 - 艾综合征。根据是否存在相关的A型慢性萎缩性胃炎(A-CAG),鉴定出了具有独特病理和发病机制特征的两种类癌变体。在19例病例中发现了A型慢性萎缩性胃炎,这些病例表现为单发或多发肿瘤,肿瘤扩展局限于黏膜或黏膜下层,肿瘤外黏膜存在一致的内分泌细胞前驱变化,以及一致的高胃泌素血症和/或G细胞增生。除两例单发性类癌外,所有病例的相关前驱病变均仅为增生性,而除一例多发性类癌外,所有病例的相关前驱病变也有发育异常。在非萎缩性黏膜中发生的4个肿瘤均为单发,侵袭性更强,且与肿瘤外内分泌细胞增殖或胃泌素分泌过多的体征无关。肿瘤细胞对嗜铬粒蛋白A和突触素呈弥漫性免疫反应,但对嗜铬粒蛋白B或HISL-19通常呈阴性。在10个类癌中发现了散在的5-羟色胺细胞。它们在浸润性肿瘤中比在黏膜内肿瘤中更常见,含胰多肽细胞的情况也较少,而含α亚基的细胞则相反。这些结果与肿瘤发病机制相关,可能为患者采用侵袭性较小的治疗方法提供理论依据。

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