Benign neoplasm: Endocrine pancreas

Description

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) (see these terms).

Data source
FinnGen phenocode CD2_BENIGN_ENDOCRINE_PANCREAS
Hospital Discharge registry ICD-10: D137
Cause of Death registry ICD-10: D137
Level in the ICD-hierarchy 3
First defined in version DF2
Ontology
DOID 1799
GWAS catalog 1000045

Key figures

Sex All Female Male
Number of individuals 22 10 12
Unadjusted prevalence (%) 0.02 0.01 0.02
Mean age at first event (years) 57.9 50.8 63.82
Median number of events / individual 1 1 1

Clinical metrics

Sex All Female Male
Recurrence within 6 months (%) 31.82 30.0 33.33
Case fatality at 5-years (%) 9.09 20.0 0.0

Associations