| Literature DB >> 18051739 |
M M Mehndiratta1, P Phul, A K Singh, S Garg, Renu Bali.
Abstract
Idiopathic granulomatous hypophysitis is a rare entity. The usual clinical presentation is that of an expanding mass lesion with varying degree of hypopituitarism. This patient described presented to us with severe headache along with panhypopituitarism and post-operative diabetes insipidus.Entities:
Mesh:
Year: 2007 PMID: 18051739
Source DB: PubMed Journal: J Assoc Physicians India ISSN: 0004-5772