Peutz-Jeghers syndrome: a report of 5 cases

Wang Xingwei 1; Fan Chaoqiang 1; Que Dan 2; Guo Hong 1; Wang Lei 1; Ling Xianlong 1; Deng Lei 1; Zhao Xiaoyan 1 1 Department of Gastroenterology; Xinqiao Hospital; Third Military Medical University; Chongqing 400037; China 2 12th Student Team; Third Military Medical University; Chongqing 400037; China

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Peutz-Jeghers syndrome: a report of 5 cases

Updated：2026-03-12

- Peutz-Jeghers syndrome: a report of 5 cases
- Peutz-Jeghers syndrome: a report of 5 cases
- 解放军医学杂志（英文版） 2011年26卷第4期页码：238-241
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  中图分类号： R735.3
- 纸质出版：2011
- Accepted：
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Peutz-Jeghers syndrome: a report of 5 cases[J]. 解放军医学杂志（英文版）, 2011,26(4):238-241.

[1].Peutz-Jeghers syndrome: a report of 5 cases[J].Journal of Medical Colleges of PLA,2011,26(04):238-241.
Peutz-Jeghers syndrome: a report of 5 cases[J]. 解放军医学杂志（英文版）, 2011,26(4):238-241. DOI：

[1].Peutz-Jeghers syndrome: a report of 5 cases[J].Journal of Medical Colleges of PLA,2011,26(04):238-241. DOI：

摘要

Abstract

Peutz-Jeghers syndrome （PJS）

also known as hereditary intestinal polyposis syndrome

is an autosomal dominant genetic disease characterized by the development of benign hamartomatous polyps in the gastrointestinal tract and hyperpigmented macules on the lips and oral mucosa. Here

we reported 5 cases of PJS and our experience about its diagnosis and treatment.

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