Case report of multiple rectal neuroendocrine tumors in a context of ulcerative colitis
- PMID: 35091352
- PMCID: PMC8803596
- DOI: 10.1016/j.ijscr.2022.106760
Case report of multiple rectal neuroendocrine tumors in a context of ulcerative colitis
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.
Keywords: Inflammatory bowel disease; Rectal neuroendocrine tumor; Ulcerative colitis.
Copyright © 2022. Published by Elsevier Ltd.
Conflict of interest statement
All authors disclose no financial and personal relationships with other people or organizations that could inappropriately influence (bias) this work.
The authors declare no conflict of interest.
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