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Case report of multiple rectal neuroendocrine tumors in a context of ulcerative colitis

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, giv...

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Detalles Bibliográficos
Autores principales: Manhal, Kalaji, Christophe, Remue, Radu, Bachmann, Daniel, Leonard, Jeremy, Schoelinck, Alex, Kartheuser
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8803596/
https://www.ncbi.nlm.nih.gov/pubmed/35091352
http://dx.doi.org/10.1016/j.ijscr.2022.106760
Descripción
Sumario: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.