Results 51 to 60 of about 172,093 (166)

Adult Onset Still’s Disease: A Case Report with a Rare Clinical Manifestation and Pathophysiological Correlations

Case Reports in Medicine, 2013
Adult-onset Still’s disease is an inflammatory multisystemic disease of unknown etiology. Pleuritis is the most common pulmonary manifestation and pleural effusions are usually exudates with a predominance of neutrophils.
Katerina M. Antoniou, George A. Margaritopoulos, Ioannis Giannarakis, Christianna Choulaki, Nikos Fountoulakis, Nikos M. Siafakas, Prodromos Sidiropoulos   +6 more
doaj   +1 more source

Characteristics of lung cancer among patients with idiopathic pulmonary fibrosis and interstitial lung disease – analysis of institutional and population data

Respiratory Research, 2018
Background Lung Cancer is occasionally observed in patients with Idiopathic Pulmonary Fibrosis (IPF). We sought to describe the epidemiologic and clinical characteristics of lung cancer for patients with IPF and other interstitial lung disease (ILD ...
Joo Heung Yoon, Mehdi Nouraie, Xiaoping Chen, Richard H Zou, Jacobo Sellares, Kristen L Veraldi, Jared Chiarchiaro, Kathleen Lindell, David O Wilson, Naftali Kaminski, Timothy Burns, Humberto Trejo Bittar, Samuel Yousem, Kevin Gibson, Daniel J Kass   +14 more
doaj   +1 more source

A first look at the reliability, validity and responsiveness of L-PF-35 dyspnea domain scores in fibrotic hypersensitivity pneumonitis

BMC Pulmonary Medicine
Background Dyspnea impairs quality of life (QOL) in patients with fibrotic hypersensitivity pneumonitis (FHP). The Living with Pulmonary Fibrosis questionnaire (L-PF) assesses symptoms, their impacts and PF-related QOL in patients with any form of PF ...
Jeffrey J. Swigris, Kerri Aronson, Evans R. Fernández Pérez   +2 more
doaj   +1 more source

Occupational exposures in sarcoidosis: a protocol for a multicentre regional case–control study in the UK

BMJ Open Respiratory Research
Background Sarcoidosis is a multisystem granulomatous disease of unclear cause. An environmental trigger in a genetically susceptible individual resulting in immune dysregulation is suspected.
Alice Margaret Turner, Sherwood Burge, Gareth I Walters, Christopher C Huntley   +3 more
doaj   +1 more source

Remote Patient Monitoring for Managing Interstitial Lung DiseaseTake-Home Points

CHEST Pulmonary
Background: Hybrid health care delivery uses a combination of in-person and telehealth visits to deliver interstitial lung disease (ILD) care efficiently and flexibly.
Genevieve Gillett, MD, Rupal J. Shah, MD, Alison M. DeDent, MD, Erica Farrand, MD   +3 more
doaj   +1 more source

Does bronchoalveolar lavage lymphocytosis predict prognosis in fibrotic hypersensitivity pneumonitis, and is this relationship influenced by low-dose immunomodulatory therapy at the time of BAL?

Frontiers in Medicine
BackgroundBronchoalveolar lavage (BAL) lymphocytosis is associated with improved prognosis in fibrotic hypersensitivity pneumonitis (fHP), although its prognostic value is unclear in patients receiving immunomodulatory treatment.
Punchalee Kaenmuang, Punchalee Kaenmuang, Punchalee Kaenmuang, Fiammetta Danzo, Fiammetta Danzo, Simon Bax, Richard J. Hewitt, Richard J. Hewitt, Richard J. Hewitt, Maria Kokosi, Maria Kokosi, Vasileios Kouranos, Vasileios Kouranos, Felix Chua, Felix Chua, Peter M. George, Peter M. George, Gisli Jenkins, Gisli Jenkins, Athol U. Wells, Athol U. Wells, Carmel J. W. Stock, Carmel J. W. Stock, Piersante Sestini, Elisabetta A. Renzoni, Elisabetta A. Renzoni   +25 more
doaj   +1 more source

Interstitial Lung Disease [PDF]

Proceedings of the Royal Society of Medicine, 1977
openaire   +2 more sources

The role of transbronchial biopsy in the diagnosis of diffuse parenchymal lung diseases: Con

Revista Portuguesa de Pneumologia (English Edition), 2012
G.A. Margaritopoulos, A.U. Wells
doaj   +3 more sources

Factors influencing long-term outcomes in fibrotic interstitial lung disease (F-ILD) diagnosed through multidisciplinary discussion (MDD): a prospective cohort study

European Journal of Medical Research
Background The diagnostic process for fibrotic interstitial lung disease (F-ILD) is notably intricate, necessitating a multidisciplinary discussion to achieve consensus based on both clinical and radiological features.
Yu-Wan Liao, Ming-Cheng Liu, Yu-Cheng Wu, Chiann-Yi Hsu, Wen-Nan Huang, Yi-Hsing Chen, Pin-Kuei Fu   +6 more
doaj   +1 more source

Patient-centered care in pulmonary fibrosis: access, anticipate, and act

Respiratory Research
Comprehensive care integrates individual patient needs and is highly valued for patients with pulmonary fibrosis (PF). The importance of a patient-centered care approach is rooted in the unpredictable progressiveness of the disease course in PF.
Delian E. Hofman, Tonia Magrì, Catharina C. Moor, Luca Richeldi, Marlies S. Wijsenbeek, Yuko Waseda   +5 more
doaj   +1 more source