Abstract
Gastrinomas are rare neuroendocrine tumours. A 9-year-old boy who initially presented with recurrent upper abdominal pain and was managed as hyperacidity syndrome was later diagnosed to have a primary, retroperitoneal, extra pancreatic gastrinoma after an asymptomatic period of 6 years is presented. At the second presentation, the contrast-enhanced CT revealed an epigastric mass and serum gastrin was grossly elevated. A complete excision of the mass was done; histopathological evaluation showed a well-differentiated neuroendocrine tumour. At a year follow up, the child is asymptomatic and the review imaging and serum gastrin levels are normal.
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Kattepura, S., Das, K., Correa, M.M.A. et al. Giant gastrinoma in a child: case report and review. Pediatr Surg Int 24, 1083–1085 (2008). https://doi.org/10.1007/s00383-008-2216-7
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DOI: https://doi.org/10.1007/s00383-008-2216-7