Peutz-Jeghers syndrome |
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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 |
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Affiliation: | Servicio de Gastroenterología y Nutrición Pediátrica, Instituto Nacional de Pediatría (INP), Insurgentes Sur 3700-C, Col. Insurgentes Cuicuilco, 04530 México, D.F. Correo. |
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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. |
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