Journal article
Rare presentation of Wegener's granulomatosis in the pituitary gland: Case report and literature review
SM Baird, U Pratap, C McLean, CP Law, N Maartens
International Journal of Surgery Case Reports | ELSEVIER SCI LTD | Published : 2017
Abstract
Introduction Wegener's granulomatosis (WG) is a systemic vasculitis that can affect a variety of organs including ear, nose and throat, lungs and kidneys. However WG is unusual in the pituitary and rare in the central nervous system. Presentation of case A 56-year-old male with likely WG presented with polyuria and polydipsia despite six months of conservative medical management. MRI scanning revealed an enlarging heterogeneously enhancing pituitary gland. Following endoscopic transsphenoidal pituitary biopsy and debulking, final tissue pathology was diagnostic for WG in the pituitary gland. Discussion Diagnosis remains difficult but most patients present with central diabetes insipidus (CDI..
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