Subtype
Pancreatic Neuroendocrine Tumor
CI-CAN-00003588Explore in graph →
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Subtype
CI-CAN-00003588Explore in graph →
Data completeness2 / 7 dimensions
Computed from entity_counters.completeness · refreshed after each connector run
Definition
A well-differentiated, low-, intermediate-, or high-grade neoplasm with neuroendocrine differentiation that arises from the pancreatic islets (islets of Langerhans). According to the presence or absence of clinical syndromes that result from hormone hypersecretion, pancreatic neuroendocrine tumors are classified either as functional or nonfunctional.
Data updated 22 days agoSource updated 26.08e
Taxonomy
Several hierarchies coexist; edges are listed per hierarchy type with their source.
Parents
Children (16)
Anatomy
32 descendants in total; counters on this page aggregate over all of them.
Data updated 18 hours agoSource updated unknowncounters aggregate over descendants
Names
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Key figures
Each figure carries its unit, period and source; ranks link to "Why this rank?".
No registry-level ancestor: burden figures are published for the mutually exclusive top-level site groups only, and this entity does not descend from one. Global figures (IARC / GLOBOCAN) stay under license review and SEER awaits credentials.
Data updated 18 hours agoSource updated unknownregistry figures: none · counters aggregate over descendants