Literature DB >> 19956919

[Pulmonary fibrosis].

A Prasse1, J U Holle, J Müller-Quernheim.   

Abstract

Many, different diseases can result in pulmonary fibrosis and its prevalence is continuously increasing. Pulmonary fibrosis is defined by a diffuse accumulation of connective tissue in the interstitial space resulting in destruction of lung parenchyma. Older individuals are more often affected by this disease than younger. Approximately one half of all patients with pulmonary fibrosis suffer from rheumatic diseases. The classification of pulmonary fibrosis was revised 1998. Now 6 different types of interstitial pneumonia according to 6 different pathologic patterns are newly defined. Still, there is no efficient treatment known, which resolves fibrotic lung remodeling. However, immunosuppressive treatment strategies are established in pulmonary fibrosis evoked by inflammatory processes.

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Year:  2010        PMID: 19956919     DOI: 10.1007/s00108-009-2406-y

Source DB:  PubMed          Journal:  Internist (Berl)        ISSN: 0020-9554            Impact factor:   0.743


  15 in total

Review 1.  American Thoracic Society. Idiopathic pulmonary fibrosis: diagnosis and treatment. International consensus statement. American Thoracic Society (ATS), and the European Respiratory Society (ERS).

Authors: 
Journal:  Am J Respir Crit Care Med       Date:  2000-02       Impact factor: 21.405

Review 2.  [Therapy for idiopathic interstitial pneumonias: steroids--and what else?].

Authors:  A Prasse; J Müller-Quernheim
Journal:  Internist (Berl)       Date:  2006-12       Impact factor: 0.743

3.  Significance of bronchoalveolar lavage for the diagnosis of idiopathic pulmonary fibrosis.

Authors:  Shinichiro Ohshimo; Francesco Bonella; Ai Cui; Martin Beume; Nobuoki Kohno; Josune Guzman; Ulrich Costabel
Journal:  Am J Respir Crit Care Med       Date:  2009-02-26       Impact factor: 21.405

4.  High-dose acetylcysteine in idiopathic pulmonary fibrosis.

Authors:  Maurits Demedts; Juergen Behr; Roland Buhl; Ulrich Costabel; Richard Dekhuijzen; Henk M Jansen; William MacNee; Michiel Thomeer; Benoit Wallaert; François Laurent; Andrew G Nicholson; Eric K Verbeken; Johny Verschakelen; Christopher D R Flower; Frédérique Capron; Stefano Petruzzelli; Paul De Vuyst; Jules M M van den Bosch; Eulogio Rodriguez-Becerra; Giuseppina Corvasce; Ida Lankhorst; Marco Sardina; Mauro Montanari
Journal:  N Engl J Med       Date:  2005-11-24       Impact factor: 91.245

Review 5.  Smoking-related interstitial lung diseases: a concise review.

Authors:  J H Ryu; T V Colby; T E Hartman; R Vassallo
Journal:  Eur Respir J       Date:  2001-01       Impact factor: 16.671

Review 6.  Lung transplantation and interstitial lung disease.

Authors:  Raed Alalawi; Timothy Whelan; Ravinder S Bajwa; Tony N Hodges
Journal:  Curr Opin Pulm Med       Date:  2005-09       Impact factor: 3.155

7.  Mortality from pulmonary fibrosis increased in the United States from 1992 to 2003.

Authors:  Amy L Olson; Jeffrey J Swigris; Dennis C Lezotte; Jill M Norris; Carla G Wilson; Kevin K Brown
Journal:  Am J Respir Crit Care Med       Date:  2007-05-03       Impact factor: 21.405

8.  [How are interstitial lung diseases diagnosed in Germany? Results of the scientific registry for the exploration of interstitial lung diseases ("Fibrosis registry") of the WATL].

Authors:  H Schweisfurth; C Kieslich; N Satake; R Loddenkemper; N Schönfeld; I Mäder; D Treutler; W Matthiessen; C Schmidt; P Leonhardt; G Siemon; N deWall; U Gereke; U Costabel
Journal:  Pneumologie       Date:  2003-07

Review 9.  Pivotal clinical dilemmas in collagen vascular diseases associated with interstitial lung involvement.

Authors:  K M Antoniou; G Margaritopoulos; F Economidou; N M Siafakas
Journal:  Eur Respir J       Date:  2009-04       Impact factor: 16.671

Review 10.  Epidemiology of extra-articular manifestations in rheumatoid arthritis.

Authors:  C Turesson; L T H Jacobsson
Journal:  Scand J Rheumatol       Date:  2004       Impact factor: 3.641

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