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GM‐CSF antibodies in artificial stone associated silicoproteinosis: A case report and literature review

Pulmonary alveolar proteinosis (PAP) is a rare lung disease where there is accumulation of surfactant in the alveoli. It can be classified based on the underlying aetiology into three categories: primary, secondary and congenital. Autoantibodies to granulocyte‐macrophage colony‐stimulating factor (G...

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Detalles Bibliográficos
Autores principales: Khan, Shana N. S., Stirling, Robert G., Mclean, Catriona A., Russell, Prudence A., Hoy, Ryan F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9366405/
https://www.ncbi.nlm.nih.gov/pubmed/35978719
http://dx.doi.org/10.1002/rcr2.1021