[High and low grade gastric epithelial dysplasia: clinical management, endoscopic assessment of p53].

Gianni Testino, Matteo Cornaggia, Fabio De Iaco, Daniela Gada
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Abstract

Epithelial dysplasia is considered the only one true histological marker of gastric cancer. In the present study we have evaluated the real clinical importance of epithelial dysplasia divided into low-grade (70 patients, mean age 59.2 years) and high-grade (50 patients, mean age 58 years) dysplasia. Furthermore, it has been made a comparison with the corresponding endoscopic picture and an evaluation of the real meaning of p53 positivity. The clinical outcome subdivision of epithelial dysplasia was effected according to the criteria of Rugge: association with or progression to gastric cancer, persistence or regression. The endoscopic patterns have been divided into ulcerous lesions and non-ulcerous lesions. The immunohistochemical study has been carried out with the utilization of a p53 antibody (Dako, Glostrup, Denmark). From the analysis of the data it comes out that low-grade dysplasia is associated with or progressed to gastric cancer in a low percentage of cases (about 8.5%), while high-grade dysplasia is associated with or progressed to gastric cancer in a high percentage of cases (about 74%), by this proving itself to be a real histological marker of gastric cancer. The cases of epithelial dysplasia associated with or progressed to gastric cancer are significantly associated with an endoscopic picture of gastric ulcer (ulcer-cancer). Nonetheless, the cases of epithelial dysplasia in correspondence of non-ulcerous lesions have been noticed to be associated with or progressed to advanced gastric cancer. The evaluation of p53 did not positively correlate with the clinical progression of the epithelial dysplasia and with TNM classification in case of gastric cancer. Therefore, the evaluation of p53 does not represent a useful marker in the clinical practice.

[高、低度胃上皮发育不良:临床管理,内镜下p53的评估]。
上皮异常增生被认为是胃癌唯一真正的组织学标志。在本研究中,我们评估了上皮性发育不良的实际临床重要性,将其分为低度(70例,平均年龄59.2岁)和高度(50例,平均年龄58岁)发育不良。并与相应的内镜图片进行对比,评价p53阳性的真实意义。根据ruge标准对上皮异常增生的临床结果进行细分:与胃癌相关或进展,持续或消退。内镜模式分为溃疡性病变和非溃疡性病变。免疫组织化学研究利用p53抗体(Dako, Glostrup,丹麦)进行。从资料分析中发现,低级别非典型增生与胃癌相关或进展为胃癌的病例比例较低(约8.5%),而高级别非典型增生与胃癌相关或进展为胃癌的病例比例较高(约74%),这证明了它是胃癌的真正组织学标志。与胃癌相关或进展为胃癌的上皮发育不良病例与胃溃疡(溃疡-癌症)的内镜图像显著相关。尽管如此,与非溃疡性病变相对应的上皮异常增生病例已被注意到与晚期胃癌相关或进展为晚期胃癌。在胃癌病例中,p53的评价与上皮异常增生的临床进展和TNM分型无正相关。因此,p53的评估在临床实践中并不代表一个有用的指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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