Results 51 to 60 of about 13,102 (151)
Objective We evaluated baseline characteristics, treatment patterns, and outcomes in patients with systemic autoimmune rheumatic disease–associated progressive pulmonary fibrosis (SARD‐PPF) and evaluated whether outcomes differed by SARD subtype. Methods The ILD‐PRO Registry is a prospective multicenter US registry of patients with PPF.
Sonali J. Bracken +7 more
wiley +1 more source
Supplemental material, Reviewer_1_v.1 for Prognosis of combined pulmonary fibrosis and emphysema: comparison with idiopathic pulmonary fibrosis alone by Chun-guo Jiang, Qiang Fu and Chun-ming Zheng in Therapeutic Advances in Respiratory ...
Qiang Fu (129583) +2 more
core +1 more source
Analysis of external respiratory function disturbances in combined pulmonary fibrosis and emphysema
Aim. To analyze the features of indicators of the external respiration function and their dynamics in patients with a combined pulmonary fibrosis and emphysema (CPFE). Materials and methods.
Nikita V. Markov +7 more
doaj +1 more source
Combined pulmonary fibrosis and emphysema
Introduction: Pulmonary fibrosis is a disease that is characterized by an accumulation of excess fibrous connective tissue in the interstitium or alveoli. This process is called scarring. The main pathophysiological effect is reduction of oxygen supply
Aleksandrov, Veselin; Medical University of Varna +4 more
core +1 more source
Abstract Background Fibrillins provide a scaffold for elastic fiber formation, which enables lung recoil and aortic compliance. Abnormal fibrillin microfibrils, as in Marfan syndrome, lead to enlarged alveoli, vascular stiffening, and aneurysms. Our earlier studies suggested that fibrillin function depends on O‐glucosylation of its epidermal growth ...
Sanjiv Neupane +4 more
wiley +1 more source
Clinical Outcomes and Acute Exacerbation Incidence in Combined Pulmonary Fibrosis and Emphysema
This multicentre prospective study of 1016 patients demonstrated that CPFE, defined as ≥ 5% emphysema on visual CT assessment, identified a high‐risk phenotype with significantly worse 5‐year survival compared to non‐CPFE IIP patients (51.4% vs. 63.1%) and COPD patients (51.4% vs. 84.0%) and higher acute exacerbation incidence, validating international
Kazuya Tsubouchi +23 more
wiley +1 more source
Tissue Resident Memory Cells: Friend or Foe?
Tissue‐resident memory T cells (TRM cells) are specialised immune cells in barrier tissues like the lungs, skin and gut, providing rapid host defence and tumour surveillance. Their retention and differentiation are regulated by molecules such as CD69, CD103 and TGF‐β. Dysregulation of TRM cells can lead to chronic activation, driving conditions such as
Chidimma F. Chude +2 more
wiley +1 more source
Pathological and radiological correlation in an autopsy case of combined pulmonary fibrosis and emphysema [PDF]
We report an educational autopsy case of combined pulmonary fibrosis and emphysema. Radiological patterns of the upper lung were considered as mostly emphysema, but pathological observation revealed significant interstitial fibrosis of usual interstitial
Fukuoka, Junya +15 more
core +1 more source
Diffuse smoking-related lung diseases: insights from a radiologic-pathologic correlation
Cigarettes are well-recognized risk factors responsible for the emergence of a variety of pathologic conditions affecting both the airways and the lungs.
Célia Sousa +8 more
doaj +1 more source
Oral Health, Periodontitis, and Respiratory Diseases: Biological Pathways
This narrative review aims to provide a comprehensive update on the potential mechanisms by which poor oral health and periodontitis impact lung health, focusing on pneumonia, COPD, and asthma. ABSTRACT Poor oral hygiene and periodontitis influence lung diseases such as pneumonia, chronic obstructive pulmonary disease (COPD), COVID‐19, and asthma.
Raluca P. Vacaru +2 more
wiley +1 more source

