Bedoya Alvaro, Garay Jone, Sanzón Fernando, Bravo Luis E, Bravo Juan C, Correa Hernan, Craver Randall, Fontham Elizabeth, Du Joanna X, Correa Pelayo
Hospital Infantil, Pasto, Colombia.
Hum Pathol. 2003 Mar;34(3):206-13. doi: 10.1053/hupa.2003.43.
Infection with Helicobacter pylori has been recognized as a cause of gastric carcinoma. Although the neoplasia is always detected in adults, the infection starts in childhood. It has been reported that early age at first infection is a determinant of gastric cancer risk. In this study, we examined the histopathology of the gastric mucosa in infected children from a population at high risk for gastric cancer (Pasto, Colombia) and compared it with that of a lower-risk population (New Orleans, LA). Gastric biopsies obtained from antrum and corpus were stained with hematoxylin and eosin and Steiner's silver method. Immunohistochemical stains were used to identify B lymphocytes (CD20), T lymphocytes (CD3 and CD8), macrophages (CD68), and polymorphonuclear neutrophil myeloperoxidase. Morphometric techniques were used to evaluate the immunohistochemical stains. In both populations, the inflammatory lesions were seen predominantly in the antrum. Compared with children from the lower-risk populations, children from the higher-risk population exhibited more severe polymorphonuclear neutrophil infiltration, stromal and intraepithelial lymphocyte infiltration, mucus depletion, and H. pylori colonization density. Regenerative activity was significantly more marked in the lower-risk population. Morphometric analysis of immunohistochemical stains showed increased representation of T lymphocytes and macrophages in the higher-risk population. Most T lymphocytes stained positive for CD8, a marker of suppressor/cytotoxic cells. B lymphocytes were relatively more abundant in the lower-risk population. The possibility that the aforementioned characteristics of H. pylori infection in children are related to cancer risk in adults is discussed.
幽门螺杆菌感染已被确认为胃癌的一个病因。尽管肿瘤总是在成年人中被检测到,但感染始于儿童期。据报道,初次感染时的低龄是胃癌风险的一个决定因素。在本研究中,我们检查了来自胃癌高风险人群(哥伦比亚帕斯托)的受感染儿童胃黏膜的组织病理学,并将其与低风险人群(路易斯安那州新奥尔良)的进行比较。从胃窦和胃体获取的胃活检组织用苏木精和伊红以及施泰纳银染色法进行染色。免疫组织化学染色用于识别B淋巴细胞(CD20)、T淋巴细胞(CD3和CD8)、巨噬细胞(CD68)和多形核中性粒细胞髓过氧化物酶。形态计量学技术用于评估免疫组织化学染色。在这两个人群中,炎症病变主要见于胃窦。与低风险人群的儿童相比,高风险人群的儿童表现出更严重的多形核中性粒细胞浸润、基质和上皮内淋巴细胞浸润、黏液缺失以及幽门螺杆菌定植密度。低风险人群的再生活性明显更显著。免疫组织化学染色的形态计量学分析显示,高风险人群中T淋巴细胞和巨噬细胞的比例增加。大多数T淋巴细胞CD8染色呈阳性,CD8是抑制/细胞毒性细胞的标志物。B淋巴细胞在低风险人群中相对更丰富。文中讨论了儿童幽门螺杆菌感染的上述特征与成人癌症风险相关的可能性。