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- W2210368918 abstract "A 59-year-old man, ex-smoker, was diagnosed with pulmonary aspergillosis according to chest radiography findings of a fungus ball and Aspergillus fumigatus detection in the bronchial lavage fluid. Two years after anti-fungal therapy, he was diagnosed with autoimmune pulmonary alveolar proteinosis (APAP) according to a crazy paving pattern in computed tomography scans of the chest, milky bronchoalveolar lavage effluent, and positive anti-granulocyte-macrophage colony-stimulating factor (GM-CSF) autoantibody in the serum. The patient ultimately died of respiratory failure caused by APAP four months after GM-CSF therapy commenced. Aspergillus infection may thus be associated with the onset and progression of APAP and tolerance to GM-CSF therapy." @default.
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- W2210368918 date "2015-01-01" @default.
- W2210368918 modified "2023-09-24" @default.
- W2210368918 title "Autoimmune Pulmonary Alveolar Proteinosis Following Pulmonary Aspergillosis" @default.
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- W2210368918 doi "https://doi.org/10.2169/internalmedicine.54.5034" @default.
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