Gastric inflammatory myofibroblastic tumor, a rare mesenchymalneoplasm: A case report

查看全文 作　　者：Manuel Fernandez [1]Rodriguez;Pedro Joaquin Artuñedo [1]Pe;Alejandro Callejas [2]Diaz;Gala Silvestre [3]Egea;Cristián Grillo Marí[1]n;Eva Iglesias [1]Garcia;Jose Luis Lucena de La [1]Poza 机构地区：[1]Department of General and Digestive Surgery,Hospital Universitario Puerta de Hierro,Majadahonda,Madrid 28222,Spain;[2]Department of Internal Medicine,Hospital Universitario Puerta de Hierro,Majadahonda,Madrid 28222,Spain;[3]Department of Pathologycal Anatomy,Hospital Universitario Puerta de Hierro,Majadahonda,Madrid 28222,Spain 出　　处：《World Journal of Gastrointestinal Surgery》索引2023年第15卷第11期,共6页 摘　　要：BACKGROUND The inflammatory myofibroblastic tumor(IMT)is a rare mesenquimal tumor of doubtful biological behaviour.It’s characterised for affecting mainly children and young adults,although it can appear at any age,being the lungs the primary affected organ(in children it represents 20%of all primary pulmonary tumors).CASE SUMMARY We present the case of a 45 year old woman,with a computed tomography(CT)finding of injury on the anterior surface of the fundus/gastric body and a solid perigastric injury of 12 mm in the ecoendoscopy.The case is presented in the tumor committee deciding to perform a laparoscopic wedge resection.The histological diagnosis was a IMT.The diagnosis is based on imaging tests like the abdominal CT,abdominal ecography and the ecoendoscopy but to confirm the diagnosis a pathological study is necessary.CONCLUSION Due to the unpredictable nature of this tumor,surgical resection is the best therapeutic option. 关 键 词：Inflammatory myofibroblastic tumor GASTRIC Wedge resection ALK-mutation Case report