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Two cases of immunoglobulin G4 (IgG4)-related hypophysitis diagnosed without pituitary biopsy
BACKGROUND: Immunoglobulin G4-related hypophysitis (IgG4-RH) is a rare disease, diagnosis of which typically depends on histopathology following an invasive pituitary biopsy, possibly leading to permanent hypopituitarism. Herein, we report two cases of IgG4-RH with favorable responses to glucocortic...
Tallennettuna:
| Julkaisussa: | Ther Adv Endocrinol Metab |
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| Päätekijät: | , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
SAGE Publications
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7323263/ https://ncbi.nlm.nih.gov/pubmed/32637064 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2042018820924556 |
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