Protein estimation in whole lung lavage fluid in hereditary pulmonary alveolar proteinosis due to a novel GM‐CSF receptor mutation
Sign Up to like & getrecommendations! Published in 2022 at "Pediatric Pulmonology"
DOI: 10.1002/ppul.25932
Abstract: Pulmonary alveolar proteinosis (PAP) is associated with abnormal surfactant accumulation in alveoli, leading to respiratory failure if untreated. This article is protected by copyright. All rights reserved. read more here.
Keywords: estimation whole; pulmonary alveolar; whole lung; alveolar proteinosis ... See more keywords
Pediatric Lung MRI in Pulmonary Alveolar Proteinosis: An Alternative to CT as a Radiation-Free Modality
Sign Up to like & getrecommendations! Published in 2022 at "Indian Journal of Pediatrics"
DOI: 10.1007/s12098-022-04089-0
Abstract: A 9-y-old girl presented with lethargy, fatigue, and progressive exertional dyspnea for the last two–three years, and rapid breathing for the past six months. Chest radiograph showed confluent air-space opacities in both lungs. Chest computed… read more here.
Keywords: lung; alveolar proteinosis; modality; pulmonary alveolar ... See more keywords
Hematopoietic stem cell transplantation for pulmonary alveolar proteinosis associated with primary immunodeficiency disease
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DOI: 10.1007/s12185-017-2375-1
Abstract: Pulmonary alveolar proteinosis (PAP) is a rare disorder that is characterized by the excessive accumulation of surfactant-like materials in the alveoli, leading to hypoxemic respiratory failure. We describe two Japanese infants with PAP associated with… read more here.
Keywords: pulmonary alveolar; cell transplantation; primary immunodeficiency; stem cell ... See more keywords
Relevance of Pulmonary Alveolar Echinococcosis
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DOI: 10.1016/j.arbres.2019.07.014
Abstract: Abstract Background Pulmonary alveolar echinococcosis (PAE) is a chronic disease caused by Echinococcus multilocularis with very low incidence in developed countries. Methods This single-center, retrospective study included 34 patients who were diagnosed with PAE between… read more here.
Keywords: echinococcosis; relevance pulmonary; pulmonary alveolar; three patients ... See more keywords
PROGRESSION OF PULMONARY ALVEOLAR MICROLITHIASIS TO PULMONARY HYPERTENSION AND COR PULMONALE
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DOI: 10.1016/j.chest.2019.08.1597
Abstract: RONAK SHAH AND PAUL STRACHAN W E D N E S D A Y F E L L O W S C A S E R E P O R T P O S T… read more here.
Keywords: pulmonary alveolar; cor pulmonale; pulmonary hypertension; alveolar microlithiasis ... See more keywords
Autoimmune pulmonary alveolar proteinosis in an adolescent successfully treated with inhaled rhGM-CSF (molgramostim)
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DOI: 10.1016/j.rmcr.2018.02.005
Abstract: Autoimmune pulmonary alveolar proteinosis (aPAP) is a rare parenchymal lung disease characterized by accumulation of surfactant in the airways with high levels of granulocyte-macrophage colony stimulating factor (GM-CSF) antibodies in blood. Disease leads to hypoxemic… read more here.
Keywords: pulmonary alveolar; csf; alveolar proteinosis; successfully treated ... See more keywords
The effectiveness of N-acetylcysteine for an adult case of pulmonary alveolar proteinosis: A case report
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DOI: 10.1016/j.rmcr.2019.100883
Abstract: Introduction Pulmonary alveolar proteinosis is a rare disease that is characterized by accumulation of surfactant and phospholipids in the pulmonary alveoli. The current mainstay of treatment is whole lung lavage. There have been rare reports… read more here.
Keywords: pulmonary alveolar; effectiveness acetylcysteine; acetylcysteine adult; case ... See more keywords
Exacerbation of autoimmune pulmonary alveolar proteinosis that improved with lone treatment of complicating nontuberculous mycobacterial infection: A case report
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DOI: 10.1016/j.rmcr.2021.101521
Abstract: Herein, we present the case of a 63-year-old man with autoimmune pulmonary alveolar proteinosis (APAP) complicated by Mycobacterium avium complex (MAC) infection. APAP was diagnosed based on serum anti-granulocyte-macrophage colony-stimulating factor antibody, bronchoalveolar lavage fluid… read more here.
Keywords: pulmonary alveolar; case; alveolar proteinosis; autoimmune pulmonary ... See more keywords
iPSC-Derived Macrophages Effectively Treat Pulmonary Alveolar Proteinosis in Csf2rb-Deficient Mice
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DOI: 10.1016/j.stemcr.2018.07.006
Abstract: Summary Induced pluripotent stem cell (iPSC)-derived hematopoietic cells represent a highly attractive source for cell and gene therapy. Given the longevity, plasticity, and self-renewal potential of distinct macrophage subpopulations, iPSC-derived macrophages (iPSC-Mφ) appear of particular… read more here.
Keywords: pulmonary alveolar; alveolar proteinosis; ipsc derived; derived macrophages ... See more keywords
An in vitro cytotoxicities comparison of 16 priority polycyclic aromatic hydrocarbons in human pulmonary alveolar epithelial cells HPAEpiC.
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DOI: 10.1016/j.toxlet.2018.03.005
Abstract: In present study, we compared for the first time the cytotoxicities of the 16 priority polycyclic aromatic hydrocarbons (PAHs) in human pulmonary alveolar epithelial cells HPAEpiC. Moreover, we examined the effects of each PAH on… read more here.
Keywords: pulmonary alveolar; priority polycyclic; aromatic hydrocarbons; human pulmonary ... See more keywords
Statin as a novel pharmacotherapy of pulmonary alveolar proteinosis
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DOI: 10.1038/s41467-018-05491-z
Abstract: Pulmonary alveolar proteinosis (PAP) is a syndrome of reduced GM-CSF-dependent, macrophage-mediated surfactant clearance, dysfunctional foamy alveolar macrophages, alveolar surfactant accumulation, and hypoxemic respiratory failure for which the pathogenetic mechanism is unknown. Here, we examine the… read more here.
Keywords: pulmonary alveolar; alveolar macrophages; statin; alveolar proteinosis ... See more keywords