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Autor:
Lisa Lancaster, Peter Fernandes, Parag Shah, Ganesh Raghu, Hunter Gillies, Bo Kim, J.E. Loyd, Kevin R. Flaherty, Roger A. Alvarez, Jeffrey J. Swigris, Neil A. Ettinger, Steven D. Nathan, Marilyn K. Glassberg
Publikováno v:
Chest. 158(2)
Background The interstitial lung diseases include a variety of disorders, many of which are characterized by fibrotic changes (fILD). Of the fILDs, Idiopathic pulmonary fibrosis is the most common. Pulmonary hypertension (PH) frequently complicates f
Autor:
Anders Heiervang Tennøe, Cathrine Brunborg, Øyvind Midtvedt, Trond Mogens Aaløkken, Øyvind Molberg, Thor Ueland, Pål Aukrust, May Britt Lund, Anna-Maria Hoffmann-Vold, Torhild Garen, Aurelija Abraityte
Publikováno v:
Chest. 150:299-306
Markers for early identification of progressive interstitial lung disease (ILD) in systemic sclerosis (SSc) are in demand. Chemokine CCL18, which has been linked to pulmonary inflammation, is an interesting candidate, but data have not been consisten
Autor:
Geertje M. de Boer, Leon M. van den Toorn, Peter Th. W. van Hal, Carla E. M. Hollak, Rogier A.S. Hoek, Michael A. den Bakker, Dennis A. Hesselink, Laura van Dussen
Publikováno v:
Chest. 149:e1-e5
Gaucher disease (GD), a lysosomal storage disorder, may result in end-stage lung disease. We report successful bilateral lung transplantation in a 49-year-old woman with GD complicated by severe pulmonary hypertension and fibrotic changes in the lung
Autor:
Vincent Cottin, Jean-François Cordier
Publikováno v:
Chest
Chest, American College of Chest Physicians, 2009, 136 (1), pp.1-2. ⟨10.1378/chest.09-0538⟩
Chest, American College of Chest Physicians, 2009, 136 (1), pp.1-2. ⟨10.1378/chest.09-0538⟩
Combined pulmonary fibrosis and emphysema (CPFE) is a recently identified syndrome occurring almost exclusively in smokers or ex-smokers, characterized by severe dyspnea and limitation to exercise capacity. Tobacco smoking is the main etiologic facto