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A Curious Case of Ileocaecal Mass: A Curious Case of Ileocaecal Mass

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Abstract

Background: Neuroendocrine tumours (NETs) of the ileocaecal junction are uncommon neoplasms and are frequently diagnosed
incidentally. Most gastrointestinal NETs are detected on histopathological examination following surgery for presumed benign
conditions such as appendicitis. Surgical resection remains the cornerstone of management, with the extent of surgery determined by
tumour size, location, and pathological features.
Case Presentation: We report the case of a 46-year-old male who presented with recurrent abdominal pain, vomiting, and significant
weight loss. Radiological evaluation revealed an ileocaecal mass causing luminal narrowing and features of subacute intestinal
obstruction. A CT-guided biopsy suggested a low-grade neuroendocrine tumour. The patient underwent a radical right hemicolectomy.
Histopathological and immunohistochemical evaluation confirmed a well-differentiated Grade 1 neuroendocrine tumour involving
the ileocaecal junction, terminal ileum, and appendix, with regional lymph node metastasis.
Conclusion: This case highlights the diagnostic challenge posed by ileocaecal neuroendocrine tumours due to their nonspecific
presentation. Routine histopathological examination of appendectomy and right hemicolectomy specimens is essential, as clinically
occult malignancies and NETs may otherwise be missed.

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