Cronkhite–Canada syndrome tends to be accompanied by colorectal cancer: Report of seven cases

IF 1.7 Q3 GASTROENTEROLOGY & HEPATOLOGY
JGH Open Pub Date : 2024-10-02 DOI:10.1002/jgh3.70032
Masayuki Shimoyama, Hiroyoshi Iwagami, Kosuke Minaga, Takuji Akamatsu, Yoshito Uenoyama, Yukitaka Yamashita
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引用次数: 0

Abstract

Cronkhite–Canada syndrome (CCS) can be difficult to diagnose. To diagnose CCS, it is important to perform endoscopic examination for patients with chronic diarrhea, check for the presence or absence of polyposis, and evaluate inflammation in the mucosa between the polyps. This study reported seven cases of CCS. The age of the patients, which included four men and three women, ranged 48–72 years, and all patients were Asian. The most common symptom among these patients was chronic diarrhea. Three of the patients had rectal cancer. In two patients, the lesions were detected at an early stage and resected via endoscopic treatment. CCS is associated with a high risk of malignant gastrointestinal lesions, especially rectal cancers, and periodic surveillance endoscopy and careful observation are required.

Abstract Image

克朗凯特-加拿大综合征往往伴有结肠直肠癌:七个病例的报告。
克朗凯特-加拿大综合征(CCS)很难诊断。要诊断 CCS,必须对慢性腹泻患者进行内窥镜检查,检查是否存在息肉病,并评估息肉之间粘膜的炎症情况。本研究报告了 7 例慢性腹泻患者。患者年龄在 48-72 岁之间,其中男性 4 人,女性 3 人,均为亚洲人。这些患者最常见的症状是慢性腹泻。其中三名患者患有直肠癌。其中两名患者在早期发现病变,并通过内窥镜治疗进行了切除。CCS 与胃肠道恶性病变(尤其是直肠癌)的高风险相关,因此需要定期进行内镜监测和仔细观察。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JGH Open
JGH Open GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
3.40
自引率
0.00%
发文量
143
审稿时长
7 weeks
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