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Histopathology of the idiopathic interstitial pneumonias (IIP): A review
(Asian Pacific Society of Respirology, 2015)
The 2013 American Thoracic Society/European Respiratory Society consensus classification update of the idiopathic interstitial pneumonias (IIP) included several important modifications to the organization and spectrum of ...
Acute exacerbation of interstitial lung disease as a sequela of COVID-19 pneumonia
Interstitial lung disease (ILD) is a heterogeneous group of disorders characterized by
dyspnea and bilateral infiltrations of the lung. While some cases are idiopathic (e.g., idiopathic
pulmonary fibrosis), others are ...
Desaturation - distance ratio: a new concept for a functional assessment of interstitial lung diseases
(Faculdade de Medicina / USP, 2010)
INTRODUCTION: The functional evaluation has become increasingly important in the understanding and management of patients with interstitial lung diseases. The cardiopulmonary exercise test and the six-minute walk test ...
Autoimmune pulmonary proteinosis in a Chilean teenager, a rare aetiology of interstitial lung disease
(2014)
Interstitial lung disease (ILD) is rare and encompasses a heterogeneous group of diseases, and is even rarer in children than in adults. ILDs compromise more than 100 different entities, including pulmonary alveolar ...
A Case of Interstitial Lung Disease With Apical Pleural Thickening: Idiopathic Pleuroparenchymal Fibroelastosis
(Sociedad Española de Neumología y Cirugia Torácica, 2014)
Idiopathic pleuroparenchymal fibroelastosis (IPPFE) is a very rare, recently described condition, characterised by fibrotic thickening of the pleural and subpleural parenchyma, predominantly in the upper lobes.1 Clinical ...
A Case of Interstitial Lung Disease With Apical Pleural Thickening: Idiopathic Pleuroparenchymal Fibroelastosis
(Sociedad Española de Neumología y Cirugia Torácica, 2014)
Idiopathic pleuroparenchymal fibroelastosis (IPPFE) is a very rare, recently described condition, characterised by fibrotic thickening of the pleural and subpleural parenchyma, predominantly in the upper lobes.1 Clinical ...
Persistent interstitial lung abnormalities in post-covid-19 patients: A case series
(2021-01-01)
A new concept of multisystem disease has emerged as a long-term condition following mild-severe COVID-19 infection. The main symptoms of this affection are breathlessness, chest pain, and fatigue. We present here the ...
Small Airway Remodeling in Idiopathic Interstitial Pneumonias: A Pathological Study
(KARGER, 2010)
Background: Few studies have addressed small airway (SA) histopathological changes and their possible role in the remodeling process in idiopathic interstitial pneumonias. Objectives: To study morphological, morphometrical ...
Epithelial mesenchymal transition in fibroblastic foci of different fibrosing lung diseases: Repair or remodeling?
(European Respiratory Soc Journals Ltd, 2013-09-01)
Interstitial lung disease and microscopic polyangiitis in chilean patients
(Mattioli 1885, 2020)
Objective: To describe the clinical and serological patients characteristics with Microscopic Polyangiitis (MPA) and Interstitial lung disease (ILD). Methods: Of all the patients with AAV diagnosed between 2007-2017 at the ...