Pulmonary alveolar proteinosis (PAP) is an uncommon disease of the lung. Clinical manifestations and imaging findings of 4 cases of PAP are reviewed: 3 primary and 1 secondary. Clinical symptoms are usually nonspecific and long term. Characteristic imaging findings are of an alveolar consolidation process involving different areas at different times. The condition is commonly misdiagnosed as pneumonia. Bronchoalveolar lavage is the best treatment up to now. PAP should be considered first in patients with characteristic imaging findings whose clinical symptoms are usually long term and nonspecific and too mild when correlated with imaging findings.