Pancreatic endocrine tumor, also known as pancreatic neuroendocrine tumor (PNET), describes a group of endocrine tumors originating in the pancreas that are usually indolent and benign, but may have the potential to be malignant. They can be functional, exhibiting a hormonal hypersecretion syndrome, but can be non-functional presenting with non-specific symptoms and include insulinoma, glucagonoma, VIPoma, somatostatinoma (SSoma), PPoma and Zollinger-Ellison syndrome (ZES, or gastrinoma) and other ectopic hormone producing tumors (such as GRFoma).
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pancreatic delta cell neuroendocrine tumor
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small intestine neuroendocrine tumor, well differentiated, low or intermediate grade
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gastrin-producing neuroendocrine tumor
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pancreatic gastrin-producing neuroendocrine tumor
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esophageal neuroendocrine tumor
MONDO:0003649
L-cell glucagon-like peptide-producing neuroendocrine tumor
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