Publication:
Pituitary carcinoma: A clinicopathological review

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dc.contributor.authorsScheithauer, BW; Kurtkaya-Yapicier, O; Kovacs, KT; Young, WF; Lloyd, RV
dc.date.accessioned2022-03-12T17:22:20Z
dc.date.accessioned2026-01-10T20:49:23Z
dc.date.available2022-03-12T17:22:20Z
dc.date.issued2005
dc.description.abstractPITUITARY CARCINOMAS ARE rare tumors; less than 100 well-documented cases have been reported to date. Such tumors are aggressive and associated with a high mortality rate. The molecular events leading to the development of pituitary carcinomas are largely unknown. Recent studies have only begun to shed light on the probable mechanisms of tumor initiation and progression. A review of the clinicopathological and molecular genetic characteristics of pituitary carcinomas is presented.
dc.identifier.doi10.1227/01.NEU.0000157926.72826.DB
dc.identifier.eissn1524-4040
dc.identifier.issn0148-396X
dc.identifier.pubmed15854256
dc.identifier.urihttps://hdl.handle.net/11424/228405
dc.identifier.wosWOS:000229054300057
dc.language.isoeng
dc.publisherOXFORD UNIV PRESS INC
dc.relation.ispartofNEUROSURGERY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectdiagnosis
dc.subjectgenetics
dc.subjectmetastasis
dc.subjectpituitary carcinoma
dc.subjecttreatment
dc.subjectNEOPLASTIC HUMAN PITUITARIES
dc.subjectGENE-EXPRESSION
dc.subjectCORTICOTROPH CARCINOMA
dc.subjectTUMOR BEHAVIOR
dc.subjectADENOMAS
dc.subjectMETASTASES
dc.subjectGLAND
dc.subjectTUMORIGENESIS
dc.subjectINVASIVENESS
dc.subjectDISSEMINATION
dc.titlePituitary carcinoma: A clinicopathological review
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage1074
oaire.citation.issue5
oaire.citation.startPage1066
oaire.citation.titleNEUROSURGERY
oaire.citation.volume56

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