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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...

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Detalles Bibliográficos
Autores principales: Gultekin, Sakir, Kargi, Atil Y, Barrera, Francisco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9625738/
http://dx.doi.org/10.1210/jendso/bvac150.1098