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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Detalles Bibliográficos
Autores principales: Hunn, Benjamin H. M., Martin, William G., Simpson, Steven, Mclean, Catriona A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2013
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4085501/
https://www.ncbi.nlm.nih.gov/pubmed/23990347
http://dx.doi.org/10.1007/s11102-013-0510-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4085501/
https://www.ncbi.nlm.nih.gov/pubmed/23990347
http://dx.doi.org/10.1007/s11102-013-0510-4

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