Results 101 to 110 of about 9,034 (208)
Whole lung lavage for pulmonary alveolar proteinosis
A 26-year-old male presented with complaints of dry cough of six months and progressive breathlessness of three months duration. He was coughing out milky white sputum for two months and had lost 12 kg weight in two months.
Jayaraman S +5 more
doaj
Alveolar proteinosis is a disease of unknown etiology.
K. M. Shagidullina, E. I. Boglaevskaya
openaire +1 more source
La proteinosis alveolar pulmonar es una enfermedad rara, caracterizada por la acumulación de surfactante en el interior del espacio alveolar, que conduce a una alteración del intercambio gaseoso. El curso clínico es variable, abarcando desde la resolución espontánea hasta la falla respiratoria y la muerte.
Carlos Bula G. +4 more
openaire +2 more sources
Statin as a novel pharmacotherapy of pulmonary alveolar proteinosis
Pulmonary alveolar proteinosis (PAP) is associated with defective macrophage clearance of surfactant. Here, the authors show that patients with PAP have altered cholesterol-to-phospholipid ratio in their surfactant, and that more importantly, statin ...
Cormac McCarthy +13 more
doaj +1 more source
Pulmonary Alveolar Proteinosis in Children: A case series
Pulmonary Alveolar Proteinosis(PAP) is a rare disease of unknown etiology, characterized by the accumulation of proteinoceous material in the alveoli that is rich in lipid and is positive on periodic acid-Schiff(PAS) stain. PAP is rare in children.
seyyed Ahmad Tabatabaei +4 more
doaj
Acute pulmonary alveolar proteinosis due to exposure to cotton dust
Secondary pulmonary alveolar proteinosis (PAP) is rare but may occur in association with malignancy, certain infections, and exposure to inorganic or organic dust and some toxic fumes.
Thind Gurcharan
doaj
A lavagem pulmonar é uma técnica desenvolvida na década de 60 do século xx com o intuito de remoção física de material proteináceo dos brônquios, em doentes com proteinose alveolar, levando a uma melhoria clínica e funcional.
M Aguiar +6 more
doaj
Autoimmune pulmonary alveolar proteinosis (PAP) is characterized by antibodies to granulocyte–macrophage colony‐stimulating factor (GM‐CSF), alveolar macrophage dysfunction, and surfactant accumulation.
Ashesh Dhungana +6 more
doaj +1 more source
Inhaled GM-CSF in neonatal mice provides durable protection against bacterial pneumonia [PDF]
Morley, S. Celeste +3 more
core +2 more sources
The transbonchial lung biopsy for diagnosis of diffuse parenchymal lung disease; Pro [PDF]
The diagnosis of diffuse parenchymal lung disease (DPLD) may require invasive procedures after all noninvasive tools have failed. The clinical context in which these diseases develop and the radiological patterns are crucial for defining the timing and ...
Cancellieri, A +7 more
core

