Web2 feb. 2024 · Approximately 50% of idiopathic inflammatory myopathies (IIMs) are associated with interstitial lung disease (ILD). Typically, IIM-ILD manifests as nonspecific … Web1 okt. 2024 · 1. Introduction. Pulmonary alveolar proteinosis (PAP) is a rare and progressive disease. This disease is characterized by the accumulation of a large …
Alveolar Proteinosis in COVID-19: Clinical Case
Web1 okt. 2024 · A pulmonary alveoli-filling disease, characterized by dense phospholipoproteinaceous deposits in the alveoli, cough, and dyspnea. This disease is … Web2 dagen geleden · Abstract. Pulmonary alveolar proteinosis (PAP) is a syndrome characterized by the accumulation of pulmonary surfactant resulting in reduced oxygen … frey vision
Autoimmune pulmonary alveolar proteinosis and idiopathic …
http://scielo.sld.cu/scielo.php?script=sci_arttext&pid=S0034-75312011000400009 WebIlektra Voulgareli, ...Clio P. Mavragani, in Handbook of Systemic Autoimmune Diseases, 2024 Lymphocytic interstitial pneumonia. Lymphocytic interstitial pneumonia, which may be considered both a lymphoproliferative disorder and an interstitial pneumonia [54, 64] is characterized by a diffuse, polyclonal lymphoid cell infiltrate surrounding airways and … Web1.Introduction. Pulmonary alveolar proteinosis (PAP), a rare diffuse lung disease characterized by surfactant lipid and protein accumulation in the air spaces, leads to impaired gas exchange through decreased levels or function of granulocyte-macrophage colony-stimulating factor (GM-CSF) and impaired surfactant processing by alveolar … freyvogel photography