首页 | 本学科首页   官方微博 | 高级检索  
     


Peutz-Jeghers syndrome
Authors:Cervantes Bustamante Roberto  Ocampo del Prado Luis Carlos  Zárate Mondragón Flora  Mata Rivera Norberto  Ramírez-Mayans Jaime A  Mora Tiscareño María Antonieta  García Campos L N
Affiliation:Servicio de Gastroenterología y Nutrición Pediátrica, Instituto Nacional de Pediatría (INP), Insurgentes Sur 3700-C, Col. Insurgentes Cuicuilco, 04530 México, D.F. Correo.
Abstract:
Peutz-Jeghers syndrome is an autonomic dominant disease characterized by hamartomatous polyps and mucocutaneous hyperpigmentation. We present 16 cases; females were more affected. The most common presenting complaints were of gastrointestinal tract. All polyps found were hamartomatous with general distribution through gastrointestinal tract. Endoscopic polypectomy should be carried out for treatment. Radiologic, endoscopic and histologic studies should be conducted for long-term follow-up, because of high risk of malignancy.
Keywords:
本文献已被 PubMed 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号