Results 31 to 40 of about 3,166 (214)
Background The differential diagnosis fibrotic hypersensitivity pneumonitis (HP) versus idiopathic pulmonary fibrosis (IPF) is important but challenging.
Sabina A. Guler +5 more
doaj +1 more source
Epidemiology of occupational hypersensitivity pneumonitis; reports from the SWORD scheme in the UK from 1996 to 2015 [PDF]
Objective To estimate the reported incidence of occupational hypersensitivity pneumonitis (OHP) in the UK and to consider whether the pattern of attributed causation has changed over time.
Burton +18 more
core +1 more source
Organic Dust Toxic Syndrome (ODTS)
Organic dust toxic syndrome (ODTS) was manifestation of some acute symptoms, (same with acute hypersensitivity pneumonitis or extrinsic allergic alveolitis) with initially by flu like syndrome that were fever, malaise, myalgia, dry cough, dyspnea, and ...
Deva Bachtiar, Agus Dwi Susanto
doaj +1 more source
Bronchoalveolar lavage in occupational lung diseases [PDF]
Occupational lung diseases (OLDs) are related to the exposure and inhalation of organic, inorganic, and synthetic particles, fumes, gases, or infectious agents. From the long list of OLDs this article focuses the discussion on bronchoalveolar lavage (BAL)
Alfaro, TM +3 more
core +1 more source
Allergy, Volume 76, Issue 5, Page 1588-1591, May 2021.
Roy Gerth van Wijk +6 more
wiley +1 more source
Hypersensitivity pneumonitis - experiences in treatment so far and opening up new possibilities [PDF]
Introduction/Objective. Hypersensitivity pneumonitis is a diagnostic and therapeutic challenge. It occurs due to an excessive immune response to inhaling an antigen (bacteria, fungi, or protozoa) to which the patient was previously sensitized. This study
Vujičić Emilija +7 more
doaj +1 more source
Features of humidifier lung and comparison with summer‐type hypersensitivity pneumonitis
Respirology, Volume 26, Issue 4, Page 394-395, April 2021.
Masafumi Shimoda +8 more
wiley +1 more source
Progressive fibrotic interstitial lung disease [PDF]
Many interstitial lung diseases (ILDs) share mechanisms that result in a progressive fibrosing phenotype. In Brazil, the most common progressive fibrosing interstitial lung diseases (PF-ILDs) are chronic hypersensitivity pneumonitis, idiopathic pulmonary
Carlos A C Pereira +2 more
doaj +1 more source
Cosmetic Talc-Related Pulmonary Granulomatosis. [PDF]
Inhalation of cosmetic talc can lead to pulmonary foreign-body granulomatosis, though fewer than 10 cases of inhaled cosmetic talc-related pulmonary granulomatosis have been reported in adults.
Adams, Jason Y +3 more
core +1 more source
Diagnosis of Fibrotic Hypersensitivity Pneumonitis: Is There a Role for Biomarkers?
Hypersensitivity pneumonitis is a complex interstitial lung syndrome and is associated with significant morbimortality, particularly for fibrotic disease.
João O. Pereira +4 more
doaj +1 more source

