Pulmonary Alveolar Proteinosis due to Familial Myelodysplastic Syndrome with resolution after stem cell transplant

Pulmonary alveolar proteinosis (PAP) is a rare lung disease with an incidence of 0.2 cases per million. PAP has multiple causes, including autoimmune, hereditary, congenital, or secondary. The latter includes hematologic conditions and exposure to different kinds of dust. Most patients present fever...

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Detalles Bibliográficos
Autores principales: Basheer, Amjad, Padrao, Eduardo Messias Hirano, Huh, Kangwook, Parker, Susan, Shah, Tejal, Gerardi, Daniel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hospital Universitário da Universidade de São Paulo 2022
Materias:
Clinical Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9135379/
https://www.ncbi.nlm.nih.gov/pubmed/35642204
http://dx.doi.org/10.4322/acr.2021.382

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9135379/
https://www.ncbi.nlm.nih.gov/pubmed/35642204
http://dx.doi.org/10.4322/acr.2021.382

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