Literature DB >> 9388826

Acquired hypophysitis in adolescence.

H J Heinze1, B B Bercu.   

Abstract

Lymphocytic and granulomatous hypophysitis are rare causes of anterior pituitary dysfunction, diabetes insipidus and hyperprolactinemia. The clinical, radiographic, and laboratory features of hypophysitis in two adolescent girls are presented along with a review of the medical literature. These subjects represent the youngest cases of autoimmune (lymphocytic) and granulomatous hypophysitis reported to date. While hypophysitis remains an unusual cause of pituitary dysfunction, it may also occur in early adolescence.

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Year:  1997        PMID: 9388826     DOI: 10.1515/jpem.1997.10.3.315

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  2 in total

Review 1.  Lymphocytic hypophysitis: disease spectrum and approach to diagnosis and therapy.

Authors:  Juan-Andres Rivera
Journal:  Pituitary       Date:  2006       Impact factor: 3.599

2.  Primary central nervous system vasculitis preceded by granulomatous hypophysitis: Case report with a review of the literature.

Authors:  Meng Huang; William J Steele; David S Baskin
Journal:  Surg Neurol Int       Date:  2015-09-28
  2 in total

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