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Bronchoalveolar Lavage Cell Data in Alveolar Proteinosis

โœ Scribed by Milleron, Bernard J.; Costabel, Ulrich; Teschler, Helmut; Ziesche, Rolf; Cadranel, Jacques L.; Matthys, Heinrich; Akoun, Georges M.


Book ID
111683197
Publisher
American Thoracic Society
Year
1991
Tongue
English
Weight
290 KB
Volume
144
Category
Article
ISSN
1073-449X

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Pulmonary alveolar proteinosis (PAP) is a rare disorder characterized by surfactant component accumulation in the alveolar space. Primary PAP is likely an autoimmune disorder caused by antibodies to granulocyte-macrophage colony stimulating factor (GM-CSF). When an underlying disease causes PAP, thi