Pancreatic neuroendocrine tumor
MONDO:0019954Pancreatic 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).
Also known as: islet cell tumor, islet cell tumors - pancreas, islet cell tumors of the pancreas, islet cell tumour, islet cell tumours - pancreas, islet cell tumours of the pancreas, pancreatic NET, pancreatic neuroendocrine tumor
1556 clinical trials for this condition and its sub-types, 60 tagged with Pancreatic neuroendocrine tumor itself.
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Sub-types of Pancreatic neuroendocrine tumor
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Functional pancreatic neuroendocrine tumor 1 trial · 14 incl. sub-types
3 sub-types
- Pancreatic insulinoma 13 trials
- Pancreatic ACTH-producing neuroendocrine tumor 0 trials
- Pancreatic gastrinoma 0 trials
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Pancreatic insulin-producing neuroendocrine tumor 0 trials · 13 incl. sub-types
1 sub-type
- Pancreatic insulinoma 13 trials
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Somatostatinoma 6 trials
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Pancreatic neuroendocrine tumor G1 1 trial · 5 incl. sub-types
1 sub-type
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1 sub-type
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Glucagonoma 2 trials
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1 sub-type
- Pancreatic gastrinoma 0 trials
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PPoma 1 trial
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VIPoma 1 trial
2 sub-types
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GRFoma 0 trials
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2 sub-types
- Pancreatic non-functioning delta cell tumor 0 trials
- Pancreatic somatostatinoma 0 trials