Utility of anti-GM-CSF antibodies in the diagnosis of pulmonary alveolar proteinosis: a case report

INTRODUCTION: Pulmonary alveolar proteinosis (PAP) is a disease characterized by the accumulation of lipoprotein-aceous material in the alveoli as a consequence of deficient processing of pulmonary surfactant. It is classified into primary, secondary, and congenital forms. Primary PAP (autoimmune or...

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Detalles Bibliográficos
Autores principales: Sierra-Rivera, Antonio, Ferriz-Vivancos, Jorge, Fandos-Sánchez, Marta, Timoneda-Timoneda, Pilar Teresa, Marcaida-Benito, Goitzane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Communications and Publications Division (CPD) of the IFCC 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349312/
https://www.ncbi.nlm.nih.gov/pubmed/37455842

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