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Granulomatous hypophysitis: a case of severe headache
Idiopathic granulomatous hypophysitis (GH) is an uncommon inflammatory disease of the pituitary with impairment of pituitary gland function due to infiltration by lymphocytes, plasma cells and macrophages. We report the case of a 39-year-old woman who presented with worsening of headaches for 1 mont...
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| Vydáno v: | BMJ Case Rep |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMJ Publishing Group
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5020714/ https://ncbi.nlm.nih.gov/pubmed/27613264 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2016-216395 |
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