Pituitary hyperplasia resulting from primary hypothyroidism

We report an unusual case of pituitary hyperplasia secondary to primary hypothyroidism clinically masquerading pituitary apoplexy. A 22-year-old female presented with intermittent headache, easy fatigability, facial puffiness, coarseness of facial features, and hoarseness of voice for six months dur...

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Detalles Bibliográficos
Autores principales: Agrawal, Amit, Diwan, S. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3277078/
https://www.ncbi.nlm.nih.gov/pubmed/22347332
http://dx.doi.org/10.4103/1793-5482.92171

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3277078/
https://www.ncbi.nlm.nih.gov/pubmed/22347332
http://dx.doi.org/10.4103/1793-5482.92171

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