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克罗恩-加拿大综合征:一例罕见病例报告及文献复习。

Cronkhite-Canada syndrome: report of a rare case and review of the literature.

机构信息

Department of Nephrology, Juye County People's Hospital, Juye, China.

Department of Gastroenterology, Juye County People's Hospital, Juye, China.

出版信息

J Int Med Res. 2020 May;48(5):300060520922427. doi: 10.1177/0300060520922427.

Abstract

Cronkhite-Canada syndrome is rarely encountered in clinical practice. Notably, most patients with Cronkhite-Canada syndrome exhibit hypoalbuminemia. Because the cause of Cronkhite-Canada syndrome is unknown, no specific treatment method has been established. Here, we describe a 59-year-old woman with Cronkhite-Canada syndrome in whom clinical manifestations were considerably relieved after treatment with prednisone.

摘要

克罗恩-加拿大综合征在临床实践中很少见。值得注意的是,大多数克罗恩-加拿大综合征患者表现为低白蛋白血症。由于克罗恩-加拿大综合征的病因不明,尚未建立特定的治疗方法。在此,我们描述了一例 59 岁女性克罗恩-加拿大综合征患者,应用泼尼松治疗后临床症状明显缓解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94d3/7273782/34a730f27676/10.1177_0300060520922427-fig1.jpg

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