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[溃疡性结肠炎并发癌。8例日本病例分析]

[Carcinoma complicating ulcerative colitis. Analysis of 8 Japanese cases].

作者信息

Imamura S

机构信息

Second Department of Pathology, Faculty of Medicine, Kyushu University, Fukuoka.

出版信息

Fukuoka Igaku Zasshi. 1990 Jan;81(1):5-19.

PMID:2323716
Abstract

Eight patients with ulcerative colitis complicated by carcinoma were investigated histopathologically on their resected colorectal specimens. Four patients carried multiple tumors, another four patients a solitary tumor. The age at the onset of the colitis in patients with multiple carcinoma was younger in average (27 years old) than that in the patients with a solitary carcinoma (45 years old). Duration of the disease before surgery exceeded 10 years in six of the eight patients. A total of eight tumors of 10 mm or more in dimension were found in four multiple cases, six of them being located in the rectum. These tumors presented peculiar macroscopic features, such as villous, putty-like, nodular, or flat, and were advanced histopathologically, well or moderately differentiated adenocarcinomas in most cases. Six of the eight accompanied areas of epithelial dysplasia adjacent to the carcinoma, the border between carcinoma and dysplasia being vague in three of the six. All multiple cases showed active changes of ulcerative colitis or chronic inflammatory processes such as thickening of the muscularis mucosa, submucosal fibrosis and Paneth cell metaplasia in the crypts. Furthermore, all multiple cases had minute adenocarcinomas, less than 10 mm in diameter, the tumor being restricted to the mucosa or to the mucosa and submucosa. Four of the nine minute carcinomas coexisted with epithelial dysplasia, suggesting that carcinoma developed from dysplasia. On the contrary, the remaining carcinomas carried no dysplasic area with a possibility that carcinoma developed also from nondysplastic atrophic mucosa. Three of the four solitary tumors were conventional adenocarcinomas associated with chronic inflammatory or dysplastic change in the bowel. The specific stainings by lectins and high-iron-diamine (HID) gave no appreciable help in diagnosing the epithelial dysplasia because of unsettled staining results. A large number of argyrophil cells were present in dysplastic epithelia, although the number of such cells was small in carcinomas.

摘要

对8例溃疡性结肠炎合并癌患者的结直肠切除标本进行了组织病理学研究。4例患者为多发肿瘤,另外4例为单发肿瘤。多发癌患者的结肠炎发病年龄平均(27岁)比单发癌患者(45岁)年轻。8例患者中有6例术前病程超过10年。4例多发病例中共发现8个直径10mm或更大的肿瘤,其中6个位于直肠。这些肿瘤呈现出特殊的大体特征,如绒毛状、油灰样、结节状或扁平状,在大多数情况下,组织病理学上为进展期、高分化或中分化腺癌。8例中有6例在癌旁伴有上皮发育异常区域,其中6例中有3例癌与发育异常之间的边界模糊。所有多发病例均显示溃疡性结肠炎的活动改变或慢性炎症过程,如黏膜肌层增厚、黏膜下纤维化和隐窝内潘氏细胞化生。此外,所有多发病例均有直径小于10mm的微小腺癌,肿瘤局限于黏膜或黏膜及黏膜下层。9个微小癌中有4个与上皮发育异常共存,提示癌由发育异常发展而来。相反,其余的癌没有发育异常区域,有可能癌也由非发育异常的萎缩黏膜发展而来。4个单发肿瘤中有3个是与肠道慢性炎症或发育异常改变相关的传统腺癌。由于染色结果不稳定,凝集素和高铁二胺(HID)的特异性染色对诊断上皮发育异常没有明显帮助。发育异常上皮中存在大量嗜银细胞,尽管癌中此类细胞数量较少。

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