pituicytoma
An extremely rare, WHO grade I, circumscribed and slow-growing tumor that arises from the neurohypophysis or infundibulum and described in adults. It is characterized by the presence of elongated, spindle-shaped neoplastic glial cells that form storiform patterns or interlacing fascicular arrangements. Signs and symptoms include visual disturbances, headache, amenorrhea, and decreased libido. [ NCIT:C94524 ]
Term info
- UMLS:C2986550 (Orphanet:251623/e)
- Orphanet:251623 (MONDO:equivalentTo)
- EFO:1000477 (MONDO:equivalentTo)
- ONCOTREE:PTCY (MONDO:equivalentTo)
- ICD9:237.0 (MONDO:relatedTo)
- DOID:0081280 (MONDO:equivalentTo)
- NCIT:C94524 (MONDO:equivalentTo)
- SCTID:608817003 (MONDO:equivalentTo)
- ICDO:9432/1 (NCIT:C94524)
ordo_disease
An extremely rare, WHO grade I, circumscribed and slow-growing tumor that arises from the neurohypophysis or infundibulum and described in adults. It is characterized by the presence of elongated, spindle-shaped neoplastic glial cells that form storiform patterns or interlacing fascicular arrangements. Signs and symptoms include visual disturbances, headache, amenorrhea, and decreased libido.
http://purl.obolibrary.org/obo/NCIT_C94524, http://linkedlifedata.com/resource/umls/id/C2986550, http://purl.obolibrary.org/obo/DOID_0081280, http://identifiers.org/snomedct/608817003, http://purl.obolibrary.org/obo/Orphanet_251623
pituicytoma, pituicytoma (WHO grade I), posterior pituitary astrocytoma
PTCY
MONDO:0006372