Secondary Pulmonary Alveolar Proteinosis Development during the Treatment for Anti-aminoacyl-tRNA Synthetase Antibody-positive Interstitial Lung Disease
Author:
Affiliation:
1. Department of Respiratory Medicine, NHO Okayama Medical Center, Japan
Publisher
Japanese Society of Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/advpub/0/advpub_3327-23/_pdf
Reference12 articles.
1. 1. The JRS Clinical Practice Guideline for Pulmonary Alveolar Proteinosis 2022, 2022 (in Japanese).
2. 2. Akasaka K, Tanaka T, Kitamura N, et al. Outcome of corticosteroid administration in autoimmune pulmonary alveolar proteinosis: a retrospective cohort study. BMC Pulm Med 15: 88, 2015.
3. 3. Ishii H, Tazawa R, Kaneko C, et al. Clinical features of secondary pulmonary alveolar proteinosis: pre-mortem cases in Japan. Eur Respir J 37: 465-468, 2011.
4. 4. Seymour JF, Presneill JJ, et al. Pulmonary alveolar proteinosis: progress in the first 44years. Am J Respir Crit Care Med 166: 215-235, 2002.
5. 5. Imura Y, Yukawa N, Handa T, et al. Two cases of autoimmune and secondary pulmonaryalveolar proteinosis during immunosuppressive therapy in dermatomyositis with interstitial lung disease. Mod Rheumatol 28: 724-729, 2018.
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