Abstract

SummaryBackgroundsThe incidence of rectal neuroendocrine tumors (NETs) diagnosed during screening colonoscopy is rising. The features and outcomes of these patients and their difference from colonic adenocarcinoma are unknown.MethodsData on subjects who underwent screening colonoscopy as part of a health checkup during a five‐year period were retrospectively analyzed. The prevalence and outcomes of the patients with rectal NETs were evaluated. The features of the patients with histopathologically proven NET and colonic adenocarcinoma were compared.ResultsA total of 8,278 subjects were enrolled. Rectal NETs were detected and diagnosed by histopathologic analysis in 13 patients (0.16%). The mean tumor size was 0.4 ± 0.25 cm and 7.7% of the patients had chronic diarrhea. Colonic adenocarcinoma was diagnosed in 24 patients (0.29%). Patients with rectal NETs were significantly younger than those with colonic adenocarcinoma (mean age: 49.4 ± 14.2 years versus 59.5 ± 11.5 years, p = 0.033) and had fewer symptoms (92.3% versus 41.7%, p = 0.001). All of the rectal NETs were successfully resected endoscopically by snare polypectomy or ligation‐assisted endoscopic mucosal resection. Histopathological analysis revealed WHO 2010 grade I NETs in all patients. No recurrence was detected during a mean follow‐up of 33 ± 15.2 months.ConclusionsRectal NETs are not uncommon incidental findings of the colonic malignancies during screening colonoscopy. Those were younger and more asymptomatic as compared with colonic adenocarcinoma. Using endoscopic resection can successfully remove these small tumors without recurrence.Copyright © 2017, The Gastroenterological Society of Taiwan, The Digestive Endoscopy Society of Taiwan and Taiwan Association for the Study of the Liver.

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