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加德纳综合征合并十二指肠球部癌:病例报告

Gardner's syndrome associated with carcinoma of the duodenal bulb: report of a case.

作者信息

Itoh H, Iida M, Kuroiwa S, Shigematsu A, Nakayama F

出版信息

Am J Gastroenterol. 1985 Apr;80(4):248-50.

PMID:3984991
Abstract

A 49-year-old woman with Gardner's syndrome, who underwent total proctocolectomy in 1982, was found to have a cancer of the duodenal bulb. Subsequently, resection of the stomach and duodenal bulb was performed in 1983. The surgical specimen showed an ulcerating tumor in the duodenal bulb which was a moderately differentiated adenocarcinoma histologically. Multiple adenomas were present in the gastric antrum and the duodenum. Duodenal cancer so far reported has been mostly confined to the periampullary region, and cancer of the duodenal bulb associated with familial polyposis coli has not been reported.

摘要

一名49岁患有加德纳综合征的女性,于1982年接受了全直肠结肠切除术,之后被发现患有十二指肠球部癌。随后,于1983年进行了胃和十二指肠球部切除术。手术标本显示十二指肠球部有一个溃疡性肿瘤,组织学检查为中度分化腺癌。胃窦和十二指肠存在多个腺瘤。迄今为止报道的十二指肠癌大多局限于壶腹周围区域,而与家族性结肠息肉病相关的十二指肠球部癌尚未见报道。

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