Aziret, MehmetÇetinkunar, SüleymanAktaş, ElifeIrkorucu, OktayBali, İlhanErdem, Hasan2022-05-112022-05-1120151941-5923https://hdl.handle.net/20.500.11776/8145Objective: Rare disease Background: Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors in the gastrointestinal system. These types of tumors originate from any part of the tract as well as from the intestine, colon, omentum, mesentery or retroperitoneum. GIST is a rare tumor compared to other types of tumors, accounting for less than 1% of all gastrointestinal tumors. Case Report: A 56-year-old male patient was hospitalized due to an upper gastrointestinal hemorrhage and the start of abdominal pain on the same day. In the upper gastrointestinal endoscopy that was performed, a solitary mass was found in the second section of the duodenum and a blood vessel (Forrest type 2a) was seen. The extent and location of the mass was detected by abdominal tomography. After hemodynamic recovery, a Whipple procedure was performed without any complications. A subsequent histopathological examination detected a c-kit-positive (CD117) pancreatic GIST with high mitotic index. Conclusions: The most effective treatment method for GISTs is surgical resection. In patients with a head of pancreatic GIST, the Whipple procedure can be used more safely and effectively.eninfo:eu-repo/semantics/openAccessGastrointestinal Stromal TumorsPancreaticoduodenectomyReceptor Protein-Tyrosine KinasesImatinib MesylateResistanceResectionPatientEraReview Article16509513N/AWOS:0003743300001102-s2.0-8493877112426237079Q3