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首页> 外文期刊>American Journal of Surgical Pathology >Diagnostic Challenges Caused by Endoscopic Biopsy of Colonic Polyps A Systematic Evaluation of Epithelial Misplacement With Review of Problematic Polyps From the Bowel Cancer Screening Program, United Kingdom
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Diagnostic Challenges Caused by Endoscopic Biopsy of Colonic Polyps A Systematic Evaluation of Epithelial Misplacement With Review of Problematic Polyps From the Bowel Cancer Screening Program, United Kingdom

机译:结肠息肉的内窥镜活检引起的诊断挑战上皮错位的系统评价,并从英国肠癌筛查计划中对有问题的息肉进行回顾

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Endoscopic mucosal biopsy may misplace mucosal elements into the submucosa of colonic adenomas, mimicking invasive adenocarcinoma. Biopsy-related misplacement can be more challenging to recognize than typical misplaced epithelium (pseudoinvasion) in pedunculated polyps. We compared the features of 16 polyps with biopsy-related misplaced epithelium with those of 10 adenomas with pseudoinvasion and 10 adenomas with invasive adenocarcinoma and performed Ki67 and p53 immunostaining on all cases. Features of misplaced epithelium in polyps referred to the Bowel Cancer Screening Program Expert Board in the United Kingdom were also evaluated for the same morphologic features. Biopsy-related epithelial misplacement occurred in adenomas throughout the colon and often appeared infiltrative (69%), including epithelial cells singly dispersed within reactive fibroinflammatory stroma or granulation tissue (44%). Misplaced epithelium displayed only low-grade cytologic features and was associated with extruded mucin (75%), tattoo pigment (63%), and misplaced normal glands (38%); scant lamina propria and muscularis mucosae were often present (88% and 44%, respectively). Cases referred to the Bowel Cancer Screening Program Expert Board also contained infiltrative-appearing misplaced epithelium (91%) that was cytologically low grade (72%), contained nondysplastic glands (11%), and showed other signs of injury. In contrast, misplaced epithelium in pedunculated polyps always had a lobular contour with a rim of lamina propria, hemorrhage, and/or hemosiderin. Invasive carcinomas showed malignant cytology and desmoplasia; most (70%) lacked features of trauma. Ki67 and p53 staining was patchy and weak in the misplaced epithelium, whereas invasive carcinomas showed increased staining for one or both markers. Pathologists should be aware that endoscopically manipulated adenomas may contain misplaced epithelium that simulates malignancy.
机译:内窥镜黏膜活检可能会将黏膜成分错位到结肠腺瘤的黏膜下层,模仿浸润性腺癌。与有蒂息肉中典型的错位上皮(假性浸润)相比,活检相关的错位可能更难以识别。我们比较了16例活检相关错位上皮的息肉与10例假浸润腺瘤和10例浸润性腺癌腺瘤的特征,并对所有病例进行了Ki67和p53免疫染色。还评估了英国肠癌筛查计划专家委员会在息肉中错位上皮细胞的特征是否具有相同的形态学特征。活检相关的上皮错放发生在整个结肠的腺瘤中,并且经常出现浸润(69%),包括单个散布在反应性纤维炎性基质或肉芽组织中的上皮细胞(44%)。错位的上皮仅表现出低级的细胞学特征,并与粘液挤出(75%),纹身颜料(63%)和错位的正常腺体(38%)有关;经常出现固有层固有层和黏膜肌层(分别为88%和44%)。移交给肠癌筛查计划专家委员会的病例还包含浸润出现的错位上皮(91%),其细胞学上较差(72%),含有非增生性腺体(11%),并显示出其他损伤迹象。相反,带蒂息肉的上皮放错位置总是呈小叶状,边缘有固有层,出血和/或含铁血黄素。浸润性癌表现为恶性细胞学和增生;大多数(70%)缺乏创伤特征。 Ki67和p53染色在错位的上皮细胞中斑片状且微弱,而浸润性癌显示一种或两种标记物的染色增加。病理学家应意识到,内窥镜下操作的腺瘤可能包含模拟恶性肿瘤的错位上皮。

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