Gastrointestinal Stromal Tumors with KIT Mutation Coexisting with Wild-type Gastrointestinal Stromal Tumors in a Patient with Neurofibromatosis Type 1  

作　　者：Yang Li Zhi-Dong Gao Xiao-Dong Yang Ying-Jiang Ye Shan Wang Ke-Wei Jiang 

机构地区：[1]Laboratory of Surgical Oncology, Peking University People's Hospital, Beijing 100044, China [2]Department of Gastrointestinal Surgery, Peking University People's Hospital, Beijing 100044, China

出　　处：《Chinese Medical Journal》2018年第18期2244-2245,共2页中华医学杂志（英文版）

摘　　要：To the Editor： Neurofibromatosis type 1 （NFI） is one of the most common autosomal dominant inherited disorders with a prevalence of approximately 1 in 3000 individuals, Gastrointestinal stromal tumors （GISTs） are the most common mesenchymal tumors of the gastrointestinal tract. Studies have suggested that NF 1 associated GISTs （NF 1-GISTs） manifest at younger ages than sporadic GISTs.To the Editor： Neurofibromatosis type 1 （NFI） is one of the most common autosomal dominant inherited disorders with a prevalence of approximately 1 in 3000 individuals, Gastrointestinal stromal tumors （GISTs） are the most common mesenchymal tumors of the gastrointestinal tract. Studies have suggested that NF 1 associated GISTs （NF 1-GISTs） manifest at younger ages than sporadic GISTs.

分 类 号：Q51[生物学—生物化学] S966.4[农业科学—水产养殖]