文献类型：期刊文献

中文题名：Two different mutational types of familial gastrointestinal stromal tumors:Two case reports

作者：Xiao-Ke Wang[1];Lu-Fan Shen[2];Xin Yang[1];He Su[3];Tao Wu[3];Peng-Xian Tao[3];Hong-Ying Lv[2];Tong-Han Yao[1];Lin Yi[2];Yuan-Hui Gu[3]

第一作者：Xiao-Ke Wang

机构：[1]The First School of Clinical Medical,Gansu University of Chinese Medicine,Lanzhou 730000,Gansu Province,China;[2]School of Traditional Chinese and Western Medicine,Gansu University of Chinese Medicine,Lanzhou 730000,Gansu Province,China;[3]Department of General Surgery,Gansu Provincial Hospital,Lanzhou 730000,Gansu Province,China

第一机构：甘肃中医药大学

年份：2024

卷号：16

期号：9

起止页码：4028

中文期刊名：World Journal of Gastrointestinal Oncology

外文期刊名：世界胃肠肿瘤学杂志（英文版）（电子版）

收录：Scopus;PubMed

基金：National Natural Science Foundation of China,No.82160842;Clinical Research Project of Research Fund of Gansu Provincial Hospital,No.23GSSYD-17;General Program of the Joint Scientific Research Fund,No.23JRRA1521.

语种：英文

中文关键词：Gastrointestinal stromal tumor;Familial gastrointestinal stromal tumor;Wild-type gastrointestinal stromal tumors;PDGFRA;Imatinib;Treatment;Case report

摘要：BACKGROUND Gastrointestinal stromal tumors(GISTs)are the most common mesenchymal tumors of the gastrointestinal(GI)tract,and cases of GISTs tend to be of the disseminated type,with a global incidence of 10 to 15 cases/million each year.The rarer familial GISTs,which often represent a population,differ in screening,diagnosis,and treatment.Familial GISTs include primary familial GISTs with predominantly KIT/PDGFRA mutations and wild-type GISTs.However,whether the same genetic family has different phenotypes has not been reported.CASE SUMMARY We report two cases of rare GISTs in the same family:A male patient with the V561D mutation in exon 12 of the PDGFRA gene,who has been taking the targeted drug imatinib since undergoing surgery,and a female patient diagnosed with wild-type GIST,who has been taking imatinib for 3 years since undergoing surgery.The favorable prognosis of these patients during the 7-year follow-up period validates the accuracy of our treatment strategy,and we have refined the entire process of diagnosis and treatment of familial GISTs in order to better manage this rare familial disease.CONCLUSION Different mutation types of familial GISTs in the same family are very rare,thus it is very important to make the correct diagnosis and treatment strategies according to the results of molecular detection for the management of familial GISTs.