Endocrine Abstracts

Introduction: Idiopathic granulomatous hypophysitis (IGH) is a rare inflammatory disease that may present with radiological changes in the pituitary gland. Diagnosis with non-specific syndromes becomes challenging. Secondary causes of granulomatous hypophysitis include tuberculosis, sarcoidosis, syphilis, Langerhans cell histiocytosis, GPA, and Rathke’s cleft cyst rupture. GPA is a multisystem disease, characterized by necrotizing small-vessel vasculitis, mostly affecting...