Table 3

 Clinical features of pancreatic neuroendocrine tumours

TumourSymptomsMalignancySurvival
InsulinomaConfusion, sweating, dizziness, weakness, unconsciousness, relief with eating10% of patients develop metastasesComplete resection cures most patients
GastrinomaZollinger-Ellison syndrome of severe peptic ulceration and diarrhoeaMetastases develop in 60% of patients; likelihood correlated with size of primaryComplete resection results in 10 year survival of 90%; less likely if large primary
GlucagonomaNecrolytic migratory erythema, weight loss, diabetes mellitus, stomatitis, diarrhoeaMetastases develop in 60% or more patientsMore favourable with complete resection; prolonged even with liver metastases
VIPomaWerner-Morrison syndrome of profuse watery diarrhoea with marked hypokalaemiaMetastases develop in up to 70% of patients; majority found at presentationComplete resection with five year survival of 95%; with metastases, 60%
Somatostatinomacholelithiasis; weight loss; diarrhoea and steatorrhoea. Diabetes mellitusMetastases likely in about 50% of patientsComplete resection associated with five year survival of 95%; with metastases, 60%
Non-syndromic pancreatic neuroendocrine tumourSymptoms from pancreatic mass and/or liver metastasesMetastases develop in up to 50% of patientsComplete resection associated with five year survival of at least 50%