| Literature DB >> 24071055 |
Qasim Husain1, Alexandros Zouzias2, Vivek V Kanumuri1, Jean Anderson Eloy3, James K Liu4.
Abstract
Idiopathic granulomatous hypophysitis (IGH) is an extremely rare chronic inflammatory lesion of the pituitary gland. This condition typically presents with chronic onset of headache and slow development of visual deficits. Pituitary apoplexy is a clinical syndrome characterized by sudden onset of headache, vision loss, opthalmoplegia, and signs of meningeal irritation. Although IGH has been previously described in the literature, its presentation as clinical pituitary apoplexy is novel. We report, to our knowledge, the first patient with IGH manifesting as clinical pituitary apoplexy. Physicians involved in the treatment of pituitary disease should be aware of this rare entity.Entities:
Keywords: Granulomatous hypophysitis; Macroadenoma; Pituitary apoplexy; Skull base; Transsphenoidal
Mesh:
Year: 2013 PMID: 24071055 DOI: 10.1016/j.jocn.2013.05.002
Source DB: PubMed Journal: J Clin Neurosci ISSN: 0967-5868 Impact factor: 1.961