Peutz–Jeghers syndrome with intermittent upper intestinal obstruction: A case report and review of the literature

RATIONALE: Peutz–Jeghers syndrome (PJS) is an autosomal dominant genetic syndrome characterized by a unique type of gastrointestinal hamartomatous polyp associated with oral and anal mucocutaneous pigmentations. Peutz–Jeghers polyps occur most numerously in the small intestine but frequently in the...

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Detalles Bibliográficos
Autores principales: Duan, Shou-Xing, Wang, Guang-Huan, Zhong, Jun, Ou, Wen-Hui, Fu, Ma-Xian, Wang, Fu-Sheng, Ma, Shu-Hua, Li, Jian-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
7100
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413220/
https://www.ncbi.nlm.nih.gov/pubmed/28445255
http://dx.doi.org/10.1097/MD.0000000000006538

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413220/
https://www.ncbi.nlm.nih.gov/pubmed/28445255
http://dx.doi.org/10.1097/MD.0000000000006538

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