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
MESH D007340

Key figures

Sex All Female Male
Number of individuals 34 17 17
Unadjusted prevalence (%) 0.02 0.02 0.02
Mean age at first event (years) 56.31 49.69 62.92
Case fatality at 5-years (%) 5.88 11.76 0.0

Longitudinal metrics

Sex All Female Male
Median nb. of events per indiv. 2 1 2
Recurrence at 6 months (%) 44.12 41.18 47.06

Associations

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