Literature DB >> 18051739

Granulomatous hypophysitis--an interesting and rare cause mimicking pituitary mass.

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.

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Year:  2007        PMID: 18051739

Source DB:  PubMed          Journal:  J Assoc Physicians India        ISSN: 0004-5772


  4 in total

1.  A case of idiopathic granulomatous hypophysitis.

Authors:  Chul Ho Chung; Min Soo Song; Hyun Deuk Cho; Du Shin Jeong; Yeo Joo Kim; Hack Gun Bae; Sang Jin Kim
Journal:  Korean J Intern Med       Date:  2012-09-01       Impact factor: 2.884

2.  Adult hypopituitarism: Are we missing or is it clinical lethargy?

Authors:  K S Brar; M K Garg; K M Suryanarayana
Journal:  Indian J Endocrinol Metab       Date:  2011-07

3.  Postpartum Granulomatous Hypophysitis: A Case Study, Review of the Literature, and Discussion of Pathogenesis.

Authors:  Upasana Joneja; D Craig Hooper; James J Evans; Mark T Curtis
Journal:  Case Rep Pathol       Date:  2016-08-24

Review 4.  Idiopathic granulomatous hypophysitis presenting with galactorrhea, headache, and nausea in a woman: a case report and review of the literature.

Authors:  Guive Sharifi; Mohammad Reza Mohajeri-Tehrani; Behrouz Navabakhsh; Bagher Larijani; Touraj Valeh
Journal:  J Med Case Rep       Date:  2019-11-16
  4 in total

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