Autoimmune Pulmonary Alveolar Proteinosis That Improved after a COVID-19 Episode
Author:
Affiliation:
1. Department of Internal Medicine, National Hospital Organization Kinki-Chuo Chest Medical Center, Japan
2. Clinical Research Center, National Hospital Organization Kinki-Chuo Chest Medical Center, Japan
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/62/15/62_1592-23/_pdf
Reference35 articles.
1. 1. Rosen SH, Castleman B, Liebow AA. Pulmonary alveolar proteinosis. N Engl J Med 258: 1123-1142, 1958.
2. 2. Inoue Y, Nakata K, Arai T, et al. Epidemiological and clinical features of idiopathic pulmonary alveolar proteinosis in Japan. Respirology 11: S55-S60, 2006.
3. 3. Inoue Y, Trapnell BC, Tazawa R, et al. Characteristics of a large cohort of patients with autoimmune pulmonary alveolar proteinosis in Japan. Am J Respir Crit Care Med 177: 752-762, 2008.
4. 4. Kitamura T, Tanaka N, Watanabe J, et al. Idiopathic pulmonary alveolar proteinosis as an autoimmune disease with neutralizing antibody against granulocyte/macrophage colony-stimulating factor. J Exp Med 190: 875-880, 1999.
5. 5. Uchida K, Beck DC, Yamamoto T, et al. GM-CSF autoantibodies and neutrophil dysfunction in pulmonary alveolar proteinosis. N Engl J Med 356: 567-579, 2007.
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