SciELO - Scientific Electronic Library Online

 
vol.81 issue2Therapeutic approach to electric burn with platelet rich plasma, grafts and hyperbaric oxygenation author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

  • Have no cited articlesCited by SciELO

Related links

  • Have no similar articlesSimilars in SciELO

Share


Medicina (Buenos Aires)

Print version ISSN 0025-7680On-line version ISSN 1669-9106

Abstract

PENSA, Lucila A. et al. Pulmonary alveolar proteinosis. Medicina (B. Aires) [online]. 2021, vol.81, n.2, pp.301-303. ISSN 0025-7680.

Pulmonary alveolar proteinosis (PAP) is a rare, diffuse pulmonary disease due to abnormal surfactant homeostasis. We present the case of a 69-year-old woman who was admitted to the hospital for progressive dyspnea with marked limitation in activity, and non-productive cough, of three months of evolution. Type I respiratory failure was confirmed. Chest tomography findings were interlobular and intralobular septal thickening, ground glass opacities and bilateral consolidation. Histological diagnosis was made and whole-lung lavage was performed with clinical improvement. We highlight the need to keep in mind differential diagnoses of respiratory failure and pulmonary infiltrates during COVID-19 pandemic, even rare entities such as PAP.

Keywords : Pulmonary alveolar proteinosis; Surfactant; Macrophage; Pulmonary lavage.

        · abstract in Spanish     · text in Spanish     · Spanish ( pdf )