ea0063p296 | Pituitary and Neuroendocrinology 1 | ECE2019
Dogansen Sema Ciftci
, Gunaldi Omur
, Tanrıverdi Osman
, Cakir Ilkay
, Mert Meral
Idiopathic granulomatoushypophysitis is a rare inflammatory disease which is characterized by inflammation and cellular infiltration of the pituitary gland. The infiltration may cause pituitary insufficiency, compression symptoms due to mass effect and diabetes insipidus. We report the case of a 33-year-old female patient who presenting with weakness, fatigue, amenorrhea and worsening of headaches about 3 months. The patient did not have blurring vision and polyuria-polydipsia...