Katayama Y, Kimura M, Konn M
Am J Surg Pathol. 1985 Jan;9(1):65-71. doi: 10.1097/00000478-198501000-00011.
A 52-year-old man with the clinical features of Cronkhite-Canada syndrome developed rectal cancer. Radiologic and endoscopic examinations revealed gastrointestinal polyposis. Histologic examination of the biopsied polyps showed cystic dilatation of glands with an inflammatory stroma. A later biopsy from a rectal polyp proved to be an adenocarcinoma. The totally resected colon and upper rectum had an ulcerated rectal cancer and numerous polyps; most of the polyps showed histological changes typical of the syndrome. Only three polyps had adenomatous changes at their surfaces. Adenomatous and carcinomatous changes of epithelia can occur in non-neoplastic polyposis of Cronkhite-Canada syndrome from which presumably a carcinoma can develop, as in the present case.
一名患有加拿大克朗凯特综合征临床特征的52岁男性患了直肠癌。影像学和内镜检查显示胃肠道息肉病。对活检息肉的组织学检查显示腺体囊性扩张伴炎性间质。后来对一个直肠息肉的活检证实为腺癌。完全切除的结肠和上段直肠有一个溃疡性直肠癌和许多息肉;大多数息肉显示出该综合征典型的组织学变化。只有三个息肉表面有腺瘤样改变。上皮的腺瘤样和癌样改变可发生在加拿大克朗凯特综合征的非肿瘤性息肉病中,正如本例所示,推测由此可能发展为癌。