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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Veröffentlicht in:	Internal Medicine 2022/10/15, Vol.61(20), pp.3095-3100
Hauptverfasser:	Muto, Yutaka, Hagiwara, Eri, Baba, Tomohisa, Sato, Yozo, Sakayori, Masashi, Tabata, Erina, Sekine, Akimasa, Komatsu, Shigeru, Okudela, Koji, Sayama, Koichi, Ogura, Takashi
Format:	Artikel
Sprache:	eng
Schlagworte:	Alveoli Amino Acyl-tRNA Synthetases anti-glycyl tRNA synthetase antibody Autoimmune Diseases Bronchiectasis Bronchoalveolar Lavage Embolization Hemoptysis Humans Hyperplasia Immunosuppressive agents Internal medicine interstitial lung disease Lung diseases Lung Diseases, Interstitial - complications Male Middle Aged Oxygen Oxygenation Polymyositis Polymyositis - complications Polymyositis - diagnosis pulmonary alveolar proteinosis Pulmonary Alveolar Proteinosis - complications Pulmonary Alveolar Proteinosis - diagnosis tRNA whole-lung lavage
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