Gastrinoma | |
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Micrograph of a neuroendocrine tumour of the stomach. H&E stain. | |
Specialty | General surgery |
Gastrinomas are neuroendocrine tumors (NETs), usually located in the duodenum or pancreas, that secrete gastrin and cause a clinical syndrome known as Zollinger–Ellison syndrome (ZES).[1][2][3] A large number of gastrinomas develop in the pancreas or duodenum, with near-equal frequency, and approximately 10% arise as primary neoplasms in lymph nodes of the pancreaticoduodenal region (gastrinoma triangle).[4]
Most gastrinomas are sporadic (75–80%), whereas approximately 20–25% are associated with multiple endocrine neoplasia type 1 (MEN-1).[5] Over 50% of gastrinomas are malignant and can metastasize to regional lymph nodes and liver. One fourth of gastrinomas are related to multiple endocrine neoplasia type 1, Zollinger–Ellison syndrome, peptic ulcer disease.[6]
Gastrinomas overproduce gastrin, resulting in increased gastric acid production, which in turn leads to the Zollinger-Ellison syndrome, characterized by (severe) peptic ulcers, gastroesophageal reflux and diarrhea.
Cingam Botejue Hoilat Karanchi 2022 p.
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