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PMON100 IgG4 hypophysitis with granulomatous histopathology
BACKGROUND: IgG4-related disease is characterized by a dense lymphoplasmacytic infiltrate rich in IgG4 plasma cells that may be accompanied by elevated serum IgG4 levels, presence of granulomatous histopathology with multinucleated giant cells has not been reported in patients with IgG4 related hypo...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9625738/ http://dx.doi.org/10.1210/jendso/bvac150.1098 |