Publication:
MAGNETIC-RESONANCE-IMAGING IN THE DIAGNOSIS OF IDIOPATHIC GIANT-CELL GRANULOMATOUS HYPOPHYSITIS - A RARE CAUSE OF HYPERPROLACTINEMIA

dc.contributor.authorsPAMIR, MN; ZIRH, TA; OZEK, MM; SAV, A; ERZEN, C; ERBENGI, T
dc.date.accessioned2022-03-12T16:56:03Z
dc.date.accessioned2026-01-11T08:17:38Z
dc.date.available2022-03-12T16:56:03Z
dc.date.issued1993
dc.description.abstractIdiopathic giant cell granulomatous hypophysitis is a rare disorder of pituitary gland characterised by a chronic inflammatory process. It can also be an extremely rare cause of hyperprolactinaemia. In this paper, we present our experience with two cases of idiopathic giant cell granulomatous hypophysitis manifested by hyperprolactinaemia, and their neuroradiological evaluation including preoperative MRI studies in one of them, and discuss our findings in the light of the literature.
dc.identifier.doidoiWOS:A1993KK80100006
dc.identifier.issn0028-3819
dc.identifier.pubmed8446292
dc.identifier.urihttps://hdl.handle.net/11424/226647
dc.identifier.wosWOS:A1993KK80100006
dc.language.isoeng
dc.publisherGEORG THIEME VERLAG
dc.relation.ispartofNEUROCHIRURGIA
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectGRANULOMATOUS HYPOPHYSITIS
dc.subjectHYPERPROLACTINEMIA
dc.subjectHYPOPITUITARISM
dc.titleMAGNETIC-RESONANCE-IMAGING IN THE DIAGNOSIS OF IDIOPATHIC GIANT-CELL GRANULOMATOUS HYPOPHYSITIS - A RARE CAUSE OF HYPERPROLACTINEMIA
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage25
oaire.citation.issue1
oaire.citation.startPage20
oaire.citation.titleNEUROCHIRURGIA
oaire.citation.volume36

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