Abstract Background Pulmonary alveolar proteinosis (PAP) is a rare lung disease characterized by accumulation of phospholipoproteinaceous material in the alveoli. The presentation is nonspecific but typically includes dyspnea; the spectrum of disease includes rapidly progressive hypoxic respiratory failure. Whole lung lavage (WLL) is the treatment of choice in symptomatic PAP, but transient worsening of oxygenation sometimes requires salvage modalities of support such as extracorporeal membrane oxygenation (ECMO). Granulocyte macrophage colony-stimulating factor (GM-CSF) plays a role in the pathophysiology of PAP. We highlight a case of severe PAP treated with exogenous GM-CSF and sequential lobar lavage due to the unavailability of salvage...
Alveolar proteinosis (AP) is characterized by excessive surfactant accumulation, and most cases are ...
The current mainstay of treatment for pulmonary alveolar proteinosis (PAP ) is whole-lung lavage. Th...
International audiencePAP is an ultra-rare disease in which surfactant components, that impair gas e...
Pulmonary Alveolar Proteinosis (PAP) is a rare disease, 3.2-6.7 cases per million. It is caused by P...
GM-CSF therapy in pulmonary alveolar proteinosis Treatment with granulocyte-macrophage colony stimul...
Pulmonary alveolar proteinosis (PAP) is a rare disorder in which lipoproteinaceous material is depos...
Pulmonary alveolar proteinosis is a rare condition characterized by the accumulation of lipoproteina...
Pulmonary alveolar proteinosis (PAP) is characterized by accumulation of lipoproteinaceous material ...
ABSTRACT Background: Pulmonary Alveolar Proteinosis (PAP) is a rare pulmonary disorder caused by a c...
Abstract: Pulmonary alveolar proteinosis is a rare condition characterized by the accumulation of li...
Whole lung lavage (WLL) is currently the standard therapy for pulmonary alveolar proteinosis (PAP). ...
Pulmonary Alveolar Proteinosis (PAP) is a rare syndrome characterized by pulmonary surfactant accumu...
Alveolar proteinosis can be primary or secondary. The secondary alveolar proteinosis was observed in...
Background: Pulmonary alveolar proteinosis (PAP) is a rare disease in children, characterized by int...
ABSTRACT: Pulmonary Alveolar Proteinosis (PAP) is a rare syndrome characterized by pulmonary surfact...
Alveolar proteinosis (AP) is characterized by excessive surfactant accumulation, and most cases are ...
The current mainstay of treatment for pulmonary alveolar proteinosis (PAP ) is whole-lung lavage. Th...
International audiencePAP is an ultra-rare disease in which surfactant components, that impair gas e...
Pulmonary Alveolar Proteinosis (PAP) is a rare disease, 3.2-6.7 cases per million. It is caused by P...
GM-CSF therapy in pulmonary alveolar proteinosis Treatment with granulocyte-macrophage colony stimul...
Pulmonary alveolar proteinosis (PAP) is a rare disorder in which lipoproteinaceous material is depos...
Pulmonary alveolar proteinosis is a rare condition characterized by the accumulation of lipoproteina...
Pulmonary alveolar proteinosis (PAP) is characterized by accumulation of lipoproteinaceous material ...
ABSTRACT Background: Pulmonary Alveolar Proteinosis (PAP) is a rare pulmonary disorder caused by a c...
Abstract: Pulmonary alveolar proteinosis is a rare condition characterized by the accumulation of li...
Whole lung lavage (WLL) is currently the standard therapy for pulmonary alveolar proteinosis (PAP). ...
Pulmonary Alveolar Proteinosis (PAP) is a rare syndrome characterized by pulmonary surfactant accumu...
Alveolar proteinosis can be primary or secondary. The secondary alveolar proteinosis was observed in...
Background: Pulmonary alveolar proteinosis (PAP) is a rare disease in children, characterized by int...
ABSTRACT: Pulmonary Alveolar Proteinosis (PAP) is a rare syndrome characterized by pulmonary surfact...
Alveolar proteinosis (AP) is characterized by excessive surfactant accumulation, and most cases are ...
The current mainstay of treatment for pulmonary alveolar proteinosis (PAP ) is whole-lung lavage. Th...
International audiencePAP is an ultra-rare disease in which surfactant components, that impair gas e...