Results 51 to 60 of about 889,501 (198)
Korean Guidelines for Diagnosis and Management of Interstitial Lung Diseases [PDF]
Tuberculosis and Respiratory DiseasesInterstitial lung disease (ILD) comprises a heterogeneous group of disorders characterized by interstitial compartment proliferation, inflammatory infiltration, and potential fibrosis with abnormal collagen deposition.
Chul Park +7 more
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Pulmonary Interstitial Emphysema
, 2022 Pulmonary interstitial emphysema (PIE) is a rare, abnormal pathology that occurs more commonly in neonates but can be seen in adults as well. The increased air pressure within the alveoli and alveolar airspaces can disrupt the adjacent lung interstitial ...
Anjum, Fatima, Jalota Sahota, Ruchi
core +1 more source
Pulmonary Artery Aneurysm Thrombosis with Combined Pulmonary Fibrosis and Emphysema: A Case Report [PDF]
Journal of Clinical and Diagnostic Research, 2016 We report a rare case of Pulmonary Artery Aneurysm (PAA) thrombosis with Combined Pulmonary Fibrosis and Emphysema (CPFE) with pulmonary hypertension. A 75-year-old male presented with haemoptysis, dyspnoea, clubbing and bilateral fine end inspiratory ...
Mitali Bharat Agrawal +1 more
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Association between Image Characteristics on Chest CT and Severe Pleural Adhesion during Lung Cancer Surgery. [PDF]
PLoS ONE, 2016 The aim of this study was to investigate the association between image characteristics on preoperative chest CT and severe pleural adhesion during surgery in lung cancer patients.
Kwang Nam Jin +6 more
doaj +1 more source
Advanced Science, EarlyView.High‐throughput Differential Dynamic Microscopy measures frequency‐resolved mechanical fingerprints from 3 to 10 μL$\umu{\rm L}$ mucus samples using only a few minutes of operator attention per sample. This automated analysis enables scalable mucus phenotyping for translational research by distinguishing mechanical heterogeneity among donors, disease ...
Feng Ling +18 more
wiley +1 more source
Evaluation of the Interstitial Histological Lesions in Pulmonary Langerhans Cell Histiocytosis
Türk Patoloji Dergisi, 2023 Objective: Pulmonary Langerhans cell histiocytosis is a cystic lung disease characterized by the proliferation of parenchymal dendritic cells. The disease can become chronic or even cause pulmonary fibrosis.
Halide Nur URER, Hatice DINCER
doaj +1 more source
Combined Pulmonary Fibrosis and Emphysema: When Scylla and Charybdis Ally
Cells, 2023 Combined pulmonary fibrosis and emphysema (CPFE) is a recently recognized syndrome that, as its name indicates, involves the existence of both interstitial lung fibrosis and emphysema in one individual, and is often accompanied by pulmonary hypertension.
Marija Gredic +5 more
doaj +1 more source
Arthritis &Rheumatology, EarlyView.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
Respiratory Medicine Case Reports, 2018 Myeloperoxidase antineutrophil cytoplasmic autoantibody (MPO-ANCA) is well-known as a serological marker for small-vessel vasculitis. However, when a smoker with interstitial lung disease (ILD) exhibits serum ANCA positivity without systemic vasculitis ...
Masahiro Nemoto +7 more
doaj +1 more source
Differentiating Smoking-Related Interstitial Fibrosis (SRIF) from Usual Interstitial Pneumonia (UIP) with Emphysema Using CT Features Based on Pathologically Proven Cases. [PDF]
PLoS ONE, 2016 To differentiate smoking-related interstitial fibrosis (SRIF) from usual interstitial pneumonia (UIP) with emphysema on CT in combined pulmonary fibrosis and emphysema (CPFE) patients.This study was approved by the institutional review board and informed
Kum Ju Chae +7 more
doaj +1 more source