Literature DB >> 23089377

[Hypophysitis: increasingly complex clinicopathological spectrum!].

I Allix1, V Rohmer.   

Abstract

Hypophysitis is a chronic inflammation of the pituitary gland that comprises an increasingly complex clinicopathological spectrum. Lymphocytic and granulomatous hypophysitis are the most common forms, but new variants have recently been reported such as IgG4-related hypophysitis that is identified by well-defined criteria. For the first time, hypophysitis in ANCA-associated vasculitides has been reported. Monoclonal antibodies directed against the cytotoxic T-lymphocyte antigen-4 (CTLA-4), investigated in metastatic melanoma, can induce hypophysitis. Hypophysitis's pathogenesis remains obscure but several candidate pituitary autoantigens have been described in the last decade, although none has proven useful as a diagnostic tool.
Copyright © 2012 Elsevier Masson SAS. All rights reserved.

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Year:  2012        PMID: 23089377     DOI: 10.1016/S0003-4266(12)70011-2

Source DB:  PubMed          Journal:  Ann Endocrinol (Paris)        ISSN: 0003-4266            Impact factor:   2.478


  1 in total

1.  Clinical presentation and management of hypophysitis: An observational study of case series.

Authors:  Marouan Karrou; Salma Benyakhlef; Achwak Alla; Najoua Messaoudi; Asmae Oulad Amar; Siham Rouf; Imane Kamaoui; Noureddine Oulali; Faycal Moufid; Naima Abda; Hanane Latrech
Journal:  Surg Neurol Int       Date:  2021-06-28
  1 in total

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