51. Case report of multiple rectal neuroendocrine tumors in a context of ulcerative colitis
- Author
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Kalaji Manhal, Remue Christophe, Bachmann Radu, Leonard Daniel, Schoelinck Jeremy, Kartheuser Alex, UCL - (SLuc) Centre du cancer, UCL - (SLuc) Service de chirurgie et transplantation abdominale, and UCL - SSS/IREC/CHEX - Pôle de chirgurgie expérimentale et transplantation
- Subjects
UC, ulcerative colitis ,IBD, inflammatory bowel disease ,Ulcerative colitis ,NET, neuroendocrine tumors ,Surgery ,Case Report ,Rectal neuroendocrine tumor ,Inflammatory bowel disease ,NEC, neuroendocrine carcinoma - Abstract
Introduction Neuroendocrine tumors (NETs) of the rectum are rare, with an estimated incidence of 0.1% of all colorectal cancers. However, it is crucial to diagnose NET, particularly in patients with ulcerative colitis, who seem to have a higher risk of cancerization according to recent studies, given the aggressiveness and poor prognosis of these tumors. Presentation of case We report the case of a 54-year-old man who developed multiple rectal NETs (approximately 10), measuring 1–6 mm, only 2 years after a primary diagnosis of ulcerative colitis. Discussion In the literature, all reported cases of NETs present patients with a long history of several years of inflammatory bowel disease; however, very little literature exists on this subject. Herein, we discussed the outcomes and a literature review of the pathology, prognosis, and management of NETs. Conclusion Despite advances in research on rectal NETs, many aspects about the disease remain unclear, partly due to its rarity., Highlights • A 54-year-old man developed NETs 2 years after ulcerative colitis diagnosis. • We discussed the pathology, prognosis, and management of NETs. • Ulcerative colitis seems to predispose patients to NET development. • Many aspects about multiple NETs remain unclear.
- Published
- 2021