Respiratory Medicine Case Reports · 2011 · 10 citations · 6 references
MedicineInfectious DiseasesPathologyInnate ImmunityMedical MicrobiologyPulmonologyPulmonary InfectionsPulmonary PathologyPulmonary TuberculosisRespiratory DiseaseRespiratory InfectionsRespiratory PathologyAlveolar Macrophage FunctionClinical SymptomsMacrophage Function AlterationMycobacterium Tuberculosis InfectionPulmonary Alveolar Proteinosis ImagingPulmonary Tuberculosis DiagnosisSurfactant Protein DeficiencyTuberculosis Pathology
Pulmonary alveolar proteinosis (PAP) is a rare and diffuse lung process, characterized by the presence of alveolar spaces filled with amorphous eosinophilic material. Impaired macrophage function and impaired host defence due to abnormalities of surfactant proteins may favor the growth of microorganisms. The association of alveolar proteinosis with mycobacterial infections is rarely reported. The PAP and superinfection with pulmonary tuberculosis is defined by radiologic and histopathologic in a 46 year-old patient. The patients with PAP should be monitored for superinfection. It may cause the disease progression and radiological, clinical symptoms may improve with treatment of superinfection.
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Pulmonary Alveolar Proteinosis
Samuel H. Rosen, Benjamin Castleman, Averill A. Liebow et al. · New England Journal of Medicine · 1958 · 1.2K citations
Pulmonary alveolar proteinosis: CT findings.
J. David Godwin, Néstor L. Müller, Julie E. Takasugi · Radiology · 1988 · 155 citations