Unilateral Autoimmune Pulmonary Alveolar Proteinosis with Polymyositis-related Interstitial Lung Disease
Author:
Affiliation:
1. Department of Respiratory Medicine, Kanagawa Cardiovascular and Respiratory Center, Japan
2. Department of Pathology, Yokohama City University School of Medicine, Japan
3. Department of Respiratory Medicine, Kawasaki Municipal Hospital, Japan
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/61/20/61_9015-21/_pdf
Reference22 articles.
1. 1. Bonfield TL, Russell D, Burgess S, Malur A, Kavuru MS, Thomassen MJ. Autoantibodies against granulocyte macrophage colony-stimulating factor are diagnostic for pulmonary alveolar proteinosis. Am J Respir Cell Mol Biol 27: 481-486, 2002.
2. 2. Trapnell BC, Nakata K, Bonella F, et al. Pulmonary alveolar proteinosis. Nat Rev Dis Prim 5: 16, 2019.
3. 3. Frazier AA, Franks TJ, Cooke EO, Mohammed TH, Pugatch FRD, Galvin JR. From the archives of the AFIP pulmonary alveolar proteinosis. Radiographics 28: 883-899, 2008.
4. 4. Prakash UBS, Barham SS, Carpenter HA, Dines DE, Marsh HM. Pulmonary alveolar phospholipoproteinosis: experience with 34 cases and a review. Mayo Clin Proc 62: 499-518, 1987.
5. 5. Oh SJ, Choo JY, Lee KY, Kim JH, Yeom SK. Localized pulmonary alveolar proteinosis: two case reports. Balkan Med J 31: 257-260, 2014.
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