%0 Case Reports
%T A Case of Autoimmune Pulmonary Alveolar Proteinosis with Pulmonary Fibrosis and Asbestosis-Like Features.
%A Nakamura M
%A Okamoto M
%A Fujimoto K
%A Shimizu S
%A Tominaga M
%A Tsuneyoshi S
%A Zaizen Y
%A Nouno T
%A Sakamoto S
%A Kawayama T
%A Hoshino T
%J Kurume Med J
%V 66
%N 1
%D Jul 2020 1
%M 32336733
暂无%R 10.2739/kurumemedj.MS661005
%X A 78-year-old man who had worked in the building industry visited our hospital because of groundglass opacity with smoothly thickened, intralobular interstitial lines and interlobular septal lines on chest high-resolution computed tomography (HRCT). HRCT image also showed a focal area of reticulation and pleural thickening. Lung specimens obtained by surgical lung biopsy showed accumulations of intra-alveolar periodic acid-Schiffpositive materials, usual interstitial pneumonia (UIP)-like subpleural lung fibrosis and asbestos bodies (1 body/cm2 in high-power field, ×400). Serum granulocyte-macrophage colony stimulating factor autoantibody was positive. The patient was diagnosed as having autoimmune pulmonary alveolar proteinosis (PAP) and needed differential diagnosis from secondary PAP caused from pulmonary asbestosis and UIP. Careful observation of the manifestations of pulmonary asbestosis and the progression of fibrosis using HRCT will be necessary in this patient.