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Annals of the Rheumatic Diseases 2003;62:97-99; doi:10.1136/ard.62.2.97
Copyright © 2003 BMJ Publishing Group Ltd & European League Against Rheumatism.
Annals of the Rheumatic Diseases 2003;62:97-99
© 2003 by BMJ Publishing Group & European League Against Rheumatism

LEADER

Systemic sclerosis

Predictors of end stage lung disease in systemic sclerosis

V Steen

Georgetown University, Washington DC, USA

Correspondence to:
Correspondence to:
Professor V Steen;
steenv@georgetown.edu


Recognition of the two types of lung disease is important because their predictors and treatment differ

Keywords: scleroderma; predictors; pulmonary function; manuscript submission

The first 150 words of the full text of this article appear below.

Pulmonary disease is now the leading cause of death in patients with scleroderma. Of the 2000 patients in the Pittsburgh scleroderma databank, 211 patients have died of lung disease over the past 20 years. One hundred and thirteen died from isolated pulmonary hypertension and 98 died of pulmonary interstitial fibrosis. These account for 21.5% of the 981 deaths and 44% of the scleroderma related deaths. Recently, progress has been made in the treatment of specific lung problems in scleroderma so it is imperative that we have a better understanding of the predictors of these complications. Most important is the acknowledgement and recognition that there are two types of lung disease in scleroderma which are very different in their pathogenesis, clinical associations, predictive factors, and treatment. The investigators of "Predictors of end stage lung disease in a cohort of patients with scleroderma" in this issue of the Annals admit . . . [Full text of this article]


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