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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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| Autors principals: | , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Medknow Publications & Media Pvt Ltd
2011
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3277078/ https://ncbi.nlm.nih.gov/pubmed/22347332 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1793-5482.92171 |
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