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首页> 外文期刊>Japanese Journal of Cancer Research >Paneth cell-rich flat adenoma of the rectum: report of a case.
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Paneth cell-rich flat adenoma of the rectum: report of a case.

机译:富含潘氏细胞的直肠扁平腺瘤:病例报告。

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摘要

A patient having familiar adenomatosis polyposis and an ileo-rectal anastomosis developed a flat mucosal lesion in the rectum. A punch biopsy revealed a villous adenoma with high-grade dysplasia. The subsequent surgical specimen indicated that the flat villous adenoma was rich in Paneth cells. Special stains included lysozyme muramidase (to visualize Paneth cells), MIB1 proliferation monoclonal antibody and single and multilabel immunohistochemistry for Paneth cells. Other methods included transmission electron microscopy and quantification with an image quantifier (Program Optilab 2.1) of lysozyme-stained Paneth cells. The subjective evaluation of hematoxylin-eosin-stained preparations demonstrated that the Paneth cells were mainly located in the lower half of the villi. Sections labeled with a specific stain (lysozyme muramidase) revealed more Paneth cells in the villi and electron microscopy showed even more in lysozyme-negative areas. Obviously some migrating dysplastic Paneth cells had retained their characteristic granules on their way towards the tip of the villi. Quantitative studies indicated that the lysozyme muramidase-positive material accounted for 41 of the adenomatous tissue. MIB1 revealed intense cell proliferation at the base of the adenoma and in the entire slopes of the villi. Despite the wide distribution of Paneth cells in intestinal metaplasia of the stomach, in the normal small intestine and in the large bowel with chronic inflammatory diseases, it is surprising that tumors arising in Paneth cells are extremely rare. The causes of the apparent natural resistance of Paneth cells to tumor development deserve to be investigated. This is the first case of Paneth cell-rich flat adenoma of the rectum in the literature.
机译:一名患有熟悉的腺瘤性息肉病和回肠直肠吻合术的患者在直肠中出现扁平粘膜病变。穿刺活检显示绒毛状腺瘤伴高度异型增生。随后的手术标本表明,扁平绒毛状腺瘤富含潘氏细胞。特殊染色剂包括溶菌酶壁酰胺酶(用于观察潘氏细胞)、MIB1增殖单克隆抗体以及潘氏细胞的单标记和多标记免疫组化。其他方法包括透射电子显微镜和使用图像定量器(Program Optilab 2.1)对溶菌酶染色的潘氏细胞进行定量。苏木精-伊红染色制剂的主观评价表明,潘氏细胞主要位于绒毛的下半部分。用特定染色剂(溶菌酶胞壁酰胺酶)标记的切片显示绒毛中有更多的潘氏细胞,电子显微镜检查显示溶菌酶阴性区域的潘氏细胞更多。显然,一些迁移的发育不良潘氏细胞在向绒毛尖端移动的过程中保留了其特征颗粒。定量研究表明,溶菌酶胞壁酰胺酶阳性物质占腺瘤组织的41%。MIB1 显示腺瘤底部和绒毛的整个斜坡处有强烈的细胞增殖。尽管潘氏细胞广泛分布在胃肠上皮化生、正常小肠和患有慢性炎症性疾病的大肠中,但令人惊讶的是,潘氏细胞中出现的肿瘤极为罕见。潘氏细胞对肿瘤发展具有明显的自然抗性的原因值得研究。这是文献中首例富含潘氏细胞的直肠扁平腺瘤。

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