Small intestinal neuroendocrine tumours (SI-NETs) are rare lesions with a prevalence of 1 per 100 000 patients per year
1. They typically grow slowly and without initial symptoms, resulting in the majority of patients presenting with advanced local disease, multiple primary tumours, and distant metastases
2–4. Staging of SI-NETs is of paramount importance, as curative surgery is indicated only for patients with resectable disease. In general, tumour resection is not commonly undertaken in asymptomatic patients with unresectable metastatic disease
5.