JOURNAL OF NEURO-OPHTHALMOLOGY, cilt.21, sa.1, ss.34-36, 2001 (SCI-Expanded)
A 53-year-old woman with symptoms of hypopituitarism and ophthalmoplegia was diagnosed as having idiopathic granulomatous hypophysitis and later developed bilateral optic neuritis. She responded well to steroid treatment. Granulomatous hypophysitis is a rare entity, and this is the first reported case associated with optic neuritis.