Role of granulocyte‐macrophage colony‐stimulating factor in pulmonary fibrosis following pulmonary alveolar proteinosis

Pulmonary alveolar proteinosis (PAP) is a rare diffuse lung disease characterized by accumulation of lipoproteinacious material in alveoli, with distinct features on high resolution computed tomography and biopsy. Its association with pulmonary fibrosis is infrequently encountered, and a clear under...

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Detalles Bibliográficos
Autores principales: Sha, Joy, Langton, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4969846/
https://www.ncbi.nlm.nih.gov/pubmed/27512562
http://dx.doi.org/10.1002/rcr2.159

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4969846/
https://www.ncbi.nlm.nih.gov/pubmed/27512562
http://dx.doi.org/10.1002/rcr2.159

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