期刊论文详细信息
Revista do Colégio Brasileiro de Cirurgiões
Síndrome de Peutz-Jeghers: relato de caso
Aderivaldo Coelho De Andrade2  Edílson Carvalho Júnior1  Karoline Da Silva Dantas2  Jocerlano Santos De Sousa2  Ricardo Keyson Paiva De Morais1 
[1] ,Universidade Federal do Piauí Faculdade de Medicina Hospital Getúlio Vargas
关键词: Peutz-Jeghers syndrome;    Hamartoma;    Colonic polyps;    Melanocytes;   
DOI  :  10.1590/S0100-69912008000300015
来源: SciELO
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【 摘 要 】

Peutz-Jeghers syndrome (PJS) is a dominant autosomal inherited disorder characterized by intestinal hamartomatous polyps in association with mucocutaneous melanocytic maculae. This syndrome is rare, and the frequency reaches from 1 in 60,000 to 1 in 300,000 people in the USA. The symptom presentations vary greatly in this disease. Some patients require minor clinical treatment while others undergo many hospitalizations and surgical treatments. In addition, patients with PJS have an increased risk for developing a variety of malignant tumors. The aim of the present study was to report one case studied of Peutz-Jeghers syndrome.

【 授权许可】

CC BY   
 All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License

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