Akbulut, SamiCakabay, BahriSezgin, ArsenalOzmen, Cihan2024-04-242024-04-2420100932-0067https://doi.org/10.1007/s00404-009-1102-4https://hdl.handle.net/11468/14429Gastrointestinal stromal tumors (GISTs) of the rectum are rare, and their clinical manifestations are variable. We report the case of a 23-year-old woman who was referred complaining of dyspareunia during coitus. We performed digital vaginal and rectal investigations, ultrasound, colonoscopy, and computed tomography. These examinations confirmed the presence of a lesion measuring about 6 x 5 x 5 cm in size attached to the posterolateral left rectum wall. We performed a circumanal excision, then arrived at the mass between the muscles of the pelvic floor. Pathological studies indicated that the tumor was a high-grade GIST, and was clear at the surgical margins. On follow-up, a GIST was found at the gastric fundus via an endoscopic biopsy. Imatinib treatment was initiated because the patient refused a second operation. The gastric lesion disappeared 6 months after imatinib treatment. Dyspareunia disappeared 1 month after operation.eninfo:eu-repo/semantics/closedAccessGastrointestinal Stromal TumorDyspareuniaRectumA rare cause of severe dyspareunia: a case report and literature reviewA rare cause of severe dyspareunia: a case report and literature reviewReview Article2811153155WOS:0002720176000312-s2.0-714490972691939661010.1007/s00404-009-1102-4Q2Q3