Idiopathic granulomatous hypophysitis: a systematic review of 82 cases in the literature.

Idiopathic granulomatous hypophysitis (IGH) is a rare inflammatory disease of the pituitary. There is debate in the scientific literature as to whether IGH represents a continuum of disease with lymphocytic hypophysitis or has a distinct pathogenesis. Due to the rare nature of the disease, previous...

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Detalhes bibliográficos
Main Authors: Hunn, B, Martin, W, Simpson, S, Mclean, C
Formato: Journal article
Idioma:English
Publicado em: Springer US 2014