Unilateral Autoimmune Pulmonary Alveolar Proteinosis with Polymyositis-related Interstitial Lung Disease

A 61-year-old patient with cystic bronchiectasis and bronchial artery hyperplasia in the left lung was diagnosed with polymyositis-related interstitial lung disease. After nine months of immunosuppressive therapy, he developed unilateral autoimmune pulmonary alveolar proteinosis (APAP) in the right...

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Detalles Bibliográficos
Autores principales: Muto, Yutaka, Hagiwara, Eri, Baba, Tomohisa, Sato, Yozo, Sakayori, Masashi, Tabata, Erina, Sekine, Akimasa, Komatsu, Shigeru, Okudela, Koji, Sayama, Koichi, Ogura, Takashi
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/PMC9646339/
https://www.ncbi.nlm.nih.gov/pubmed/35370233
http://dx.doi.org/10.2169/internalmedicine.9015-21

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9646339/
https://www.ncbi.nlm.nih.gov/pubmed/35370233
http://dx.doi.org/10.2169/internalmedicine.9015-21

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