Transanal total mesorectal excision for treating a lower rectal inflammatory myofibroblastic tumor: A case report

Rectal inflammatory myofibroblastic tumors are extremely rare, with no reports of their preoperative diagnosis. A 17-year-old woman who presented with low-grade fever, repeated diarrhea, constipation, and a 1-month history of anal pain was referred to our hospital. Rectal examination revealed a palpable hard mass with a smooth surface at the posterior wall 4 cm from the anal verge. Colonoscopy revealed a 4.0-cm submucosal tumor in the upper edge of the anal canal. Computed tomography and magnetic resonance imaging revealed a 5.0 x 4.0 cmsized well-defined tumor contacting the rectum. Computed tomography-guided biopsy was performed, and an inflammatory myofibroblastic tumor was diagnosed. There have been no reports of surgery for a rectal inflammatory myofibroblastic tumor using transanal total mesorectal excision. We preoperatively diagnosed the patient with an inflammatory myofibroblastic tumor in the lower rectum and achieved anorectal preservation and curative resection with transanal total mesorectal excision, providing good view of the deep pelvis.