Background: This document provides clinical recommendations for the diagnosis of
idiopathic pulmonary fibrosis (IPF). It represents a collaborative effort between the American …

Hypersensitivity pneumonitis (HP), also known as extrinsic allergic alveolitis, is a complex
syndrome of varying intensity, clinical presentation, and natural history [1, 2]. Numerous …

Background Given the phenotypic similarities between rheumatoid arthritis (RA)–associated
interstitial lung disease (ILD) (hereafter, RA-ILD) and idiopathic pulmonary fibrosis, we …

DLCO: Difusión pulmonar de monóxido de carbono. C6M: Caminata de 6 minutos. PDGF:
Factor de crecimiento derivado de las plaquetas. VEGF: Factor de crecimiento vascular …

Idiopathic pulmonary fibrosis (IPF) is a lethal lung disorder of unknown etiology. The disease
is likely the result of complex interactions between genetic and environmental factors. …

The etiology of idiopathic pulmonary fibrosis (IPF) remains poorly understood, but some studies
have suggested that cigarette smoking or other occupational or environmental exposures…

Además de la fibrosis pulmonar idiopática (FPI), otras enfermedades pulmonares intersticiales
difusas (EPID) desarrollan fibrosis pulmonar, lo cual ocurre en una proporción variable …

Objetivo Identificar las causas más frecuentes de hemorragia alveolar difusa (HAD) y conocer
la evolución de los casos durante su hospitalización. Pacientes y método Revisión de …

Background Chronic hypersensitivity pneumonitis (cHP) represents a severe lung disease
often evolving to fibrosis with the subsequent destruction of the lung parenchyma. There are …

Background: This American Thoracic Society, European Respiratory Society, Japanese
Respiratory Society, and Asociación Latinoamericana de Tórax guideline updates prior …