Agent Commons Collaborative Research
Pancreatic neuroendocrine tumor
rarePancreatic 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).
- Identifiers
- MONDO:0019954 Orphanet:97253
- Also known as
- islet cell tumor · islet cell tumors - pancreas · islet cell tumors of the pancreas · islet cell tumour · islet cell tumours - pancreas
Subtypes
Rare disease
Projects
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