pancreatic neuroendocrine tumor
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). [ ]
Term info
pancreatic neuroendocrine tumor
- Islet cell tumors of the pancreas
- islet cell tumor
- islet cell tumors - pancreas
- islet cell tumors of the pancreas
- pancreatic NET
- pancreatic neuroendocrine tumor
- well differentiated pancreatic endocrine neoplasm
- well differentiated pancreatic endocrine tumor
- well-differentiated NEN of pancreas
- well-differentiated neuroendocrine neoplasm of pancreas
- well-differentiated pancreatic NEN
- well-differentiated pancreatic neuroendocrine neoplasm
disease_grouping, ordo_group_of_disorders
http://purl.obolibrary.org/obo/NCIT_C27720, http://purl.obolibrary.org/obo/Orphanet_97253
true
neuroendocrine tumor of pancreas, PANET, pancreatic endocrine tumor
EFO:1000045
https://icd.codes/icd10cm/E16.8
Laura Huerta
Term relations
- digestive system neuroendocrine tumor, grade 1/2
- islet cell tumor
- has_disease_location some (pancreas or part of some pancreas)