Leukemia & lymphoma/Leukemia and lymphoma · 2003 · 24 citations · 16 references
Acute Lung InjuryInflammatory Lung DiseaseAdvanced Lung DiseaseConsolidation ChemotherapyImmunologyPulmonary Alveolar ProteinosisPathologyEosinophilic DisorderImmunotherapyOncologyPeriodic-acid SchiffHematologyGranulocyteG-csf TherapyPulmonary FibrosisAutoimmunityPulmonary MedicinePulmonary BlastomaLung CancerPulmonary DiseaseBronchial NeoplasmMedicine
Pulmonary alveolar proteinosis (PAP) is the intra-alveolar accumulation of periodic-acid schiff (PAS) positive material. PAP is one of the underrecognized causes of pulmonary infiltrates in patients with hematologic malignancies. Here, we present a patient with acute lymphoid leukemia (ALL) in first remission that developed fever and diffuse pulmonary infiltrates during the neutropenic stage of consolidation chemotherapy. The histopathologic examination of bronchoalveolar lavage (BAL) fluid and transbronchial biopsy specimen demonstrated the presence of PAS-positive eosinophilic material. Empirical antibiotherapy and granulocyte-colony stimulating factor (G-CSF) were given. After the correction of neutropenia with G-CSF, the patient's fever disappeared, acute phase reactants decreased, pulmonary infiltrates resolved. We present this case because it was the first patient in whom the correction of neutropenia with G-CSF was followed by resolution of PAP.
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Pulmonary Alveolar Proteinosis
Samuel H. Rosen, Benjamin Castleman, Averill A. Liebow et al. · New England Journal of Medicine · 1958 · 1.1K citations
Pulmonary Pathology, Advanced Lung Disease, Pneumothorax +14
J.A. Huffman, William M. Hull, Glenn Dranoff et al. · Journal of Clinical Investigation · 1996 · 261 citations · Full text
Inflammatory Lung Disease, Lung Inflammation, Gm-csf-hull Mutant Mice +21