AI Article Synopsis

  • Somatostatinomas are rare neuroendocrine tumors primarily found in the pancreas or duodenum, occurring at a rate of about 1 in 40 million.
  • Duodenal somatostatinomas are often linked with conditions like neurofibromatosis type 1 (NF1), and while gastrointestinal stromal tumors (GIST) can occur with NF1, their connection to somatostatinomas is rare.
  • A case study involves a patient with NF1 who experienced obstructive jaundice due to nodules near the ampulla of Vater, leading to surgery that confirmed the presence of a somatostatinoma and GIST, highlighting the need to consider these tumors in similar cases.

Article Abstract

Somatostatinomas are rare neuroendocrine tumours, mostly located in the pancreas or duodenum, with an estimated incidence of 1 in 40 million. Duodenal somatostatinomas (DSs) are usually found in association with neurofibromatosis type 1 (NF1), tuberous sclerosis and Von Hippel-Lindau syndrome. Gastrointestinal stromal tumours (GIST) have also been described in NF1, but the association with somatostatinoma is very uncommon. We report the case of a patient with NF1 who presented with obstructive jaundice due to multiple firm nodules around the ampulla of Vater. A pancreaticoduodenectomy was performed and revealed a 1 cm duodenal/ampullary mass which stained positive for somatostatin, together with a GIST also found on the duodenal wall. Despite its rarity, ampullary somatostatinomas should be considered in the differential diagnosis of biliary tract dilation in patients with NF1.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6340528PMC
http://dx.doi.org/10.1136/bcr-2018-226702DOI Listing

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