Subtype
Testicular Neuroendocrine Tumor, Prepubertal-Type
CI-CAN-00004088Explore in graph →
Non-malignant
- NCIt
- C6360
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Subtype
CI-CAN-00004088Explore in graph →
Data completeness0 / 7 dimensions
Computed from entity_counters.completeness · refreshed after each connector run
Definition
A rare, usually well-differentiated neuroendocrine neoplasm that arises from the testis. It usually affects adults, and a minority of patients have carcinoid syndrome. It may occur in isolation or, less frequently, be associated with testicular teratoma. The majority of cases are not associated with isochromosome 12p or germ cell neoplasia in situ. The clinical course is usually benign.
Data updated 22 days agoSource updated 26.08e
Taxonomy
Several hierarchies coexist; edges are listed per hierarchy type with their source.
Parents
Children (0)
Leaf node — no children.
Anatomy
Data updated 19 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 19 hours agoSource updated unknownregistry figures: none · counters aggregate over descendants