Publication:
Magnetic resonance imaging in the diagnosis of idiopathic giant-cell granulomatous hypophysitis: A rare cause of hyperprolactinaemia

dc.contributor.authorsPamir M.N., Zirh T.A., Ozek M.M., Sav A., Erzen C., Erbengi T.
dc.date.accessioned2022-03-15T01:52:58Z
dc.date.accessioned2026-01-11T17:22:36Z
dc.date.available2022-03-15T01:52:58Z
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.doi10.1055/s-2008-1052286
dc.identifier.issn283819
dc.identifier.pubmed8446292
dc.identifier.urihttps://hdl.handle.net/11424/246213
dc.language.isoeng
dc.relation.ispartofNeurochirurgia
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectgranulomatous hypophysitis
dc.subjecthyperprolactinaemia
dc.titleMagnetic resonance imaging in the diagnosis of idiopathic giant-cell granulomatous hypophysitis: A rare cause of hyperprolactinaemia
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage25
oaire.citation.issue1
oaire.citation.startPage20
oaire.citation.titleNeurochirurgia
oaire.citation.volume36

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