Molecular Subtype
GLI1-Altered Soft Tissue Tumor
CI-CAN-00002777GAESTTExplore in graph →
Non-malignant5 evidence items
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Molecular Subtype
CI-CAN-00002777GAESTTExplore in graph →
Data completeness1 / 7 dimensions
Computed from entity_counters.completeness · refreshed after each connector run
Definition
A rare mesenchymal neoplasm of uncertain histogenesis characterized by the presence of nests and sheets of neoplastic epithelioid cells separated by a rich delicate arborizing vascular network, and GLI1 gene rearrangement. It arises from soft tissue and viscera and presents as a slow-growing painless mass. The majority of cases have an indolent clinical course following complete excision. Distant metastases have been reported in a minority of cases.
Data updated 22 days agoSource updated 26.08e
Taxonomy
Several hierarchies coexist; edges are listed per hierarchy type with their source.
Parents
Children (2)
5 descendants in total; counters on this page aggregate over all of them.
Anatomy
Data updated 16 minutes 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 16 minutes agoSource updated unknownregistry figures: none · counters aggregate over descendants