Multifocal small cell neuroendocrine carcinoma of the jejunum, ileum and caecum: A rare case with intestinal obstruction and perforation

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Authors: José Richard Tenazoa-Villalobos, Edgar Fermín Yan–Quiroz, Olga Mercedes Viviana Burgos-García, Gladys Llerena-Cobián
Cited by: 0
References: 25

Abstract

Neuroendocrine tumours of the small intestine are sporadic and may be of large- or small-cell type. The ileum and jejunum are most frequently affected by this malignant neoplasm, which exhibits a high tendency towards multifocality and metastatic spread. Diagnosis is often delayed because symptoms are non-specific, such as pain, carcinoid syndrome, or anaemia. They typically occur around the age of 60 years and affect women more often than men. At diagnosis, they are frequently locally advanced with nodal involvement, leading to mesenteric fibrosis that can result in intestinal obstruction or perforation. We present the case of a 72-year-old man who, during the COVID-19 pandemic, presented with non-specific symptoms and underwent exploratory laparotomy, including partial resection of the terminal jejunum, ileum, and cecum, end-to-lateral ileocolonic anastomosis, and creation of a double-barrel jejunostomy. Multiple tumours were found in the small intestine and caecum. However, the outcome was poor due to disease progression. Neuroendocrine tumours should be considered in the differential diagnosis for colonic and small intestinal neoplasms, regardless of the patient’s age or sex. This case highlights the significant challenges faced by surgeons in managing complex, multifocal tumours.

Fields of Study & Subjects

Neuroendocrine Tumor Research Advances Gastrointestinal Bleeding Diagnosis and Treatment Gastrointestinal Tumor Research and Treatment

Publication details

Journal / source
International Journal of Gastrointestinal Intervention
Volume
15
Issue
4
Pages
218–222
Publication date
26 February 2026
Language
EN