Autoimmune pulmonary alveolar proteinosis with features similar to nonspecific interstitial pneumonia

A 58-year-old woman with cough and dyspnea who was suspected of having idiopathic interstitial pneumonia had been treated with corticosteroids and cyclosporine, but the symptoms had worsened. There were no findings to suspect pulmonary alveolar proteinosis (PAP) in the bronchoalveolar lavage fluid,...

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Detalles Bibliográficos
Autores principales: Fujii, Koki, Takeshima, Hideyuki, Nishimura, Taku, Sakatani, Toshio, Masuda, Yoshio, Morikawa, Teppei, Usui, Kazuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076885/
https://www.ncbi.nlm.nih.gov/pubmed/35535320
http://dx.doi.org/10.1016/j.rmcr.2022.101591

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076885/
https://www.ncbi.nlm.nih.gov/pubmed/35535320
http://dx.doi.org/10.1016/j.rmcr.2022.101591

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