Autoimmune Pulmonary Alveolar Proteinosis during the Treatment of Idiopathic Inflammatory Myopathy

Approximately 50% of idiopathic inflammatory myopathies (IIMs) are associated with interstitial lung disease (ILD). Typically, IIM-ILD manifests as nonspecific interstitial pneumonia. We herein report a rare case of a 78-year-old man with autoimmune pulmonary alveolar proteinosis (PAP) that develope...

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Detalles Bibliográficos
Autores principales: Shijubou, Naoki, Sawai, Takeyuki, Hatakeyama, Taku, Munakata, Satoru, Yamazoe, Masami, Chiba, Hirofumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9970810/
https://www.ncbi.nlm.nih.gov/pubmed/35831113
http://dx.doi.org/10.2169/internalmedicine.9558-22

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9970810/
https://www.ncbi.nlm.nih.gov/pubmed/35831113
http://dx.doi.org/10.2169/internalmedicine.9558-22

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