ORGAN MANIFESTATIONS IN 100 PATIENTS WITH PROGRESSIVE SYSTEMIC SCLEROSIS: A COMPARISON BETWEEN THE CREST SYNDROME AND DIFFUSE SCLERODERMA

Rheumatology ◽  
1989 ◽  
Vol 28 (4) ◽  
pp. 281-286 ◽  
Author(s):  
ANITA ÅKESSON ◽  
F. A. WOLLHEIM
2002 ◽  
Vol 6 (1) ◽  
pp. 28-32
Author(s):  
Betsie Van der Walt ◽  
Irma Van de Werke ◽  
Zarina Lockhat

Scleroderma or progressive systemic sclerosis is a diffuse disease characterised by excessive deposition of collagen and small-vessel arteritis. Systemic sclerosis is divided into two groups.1. Diffuse scleroderma, where interstitial pulmonary fibrosis is common,  and2. The CREST syndrome, which is characterised more commonly by vasculitis with pulmonary hypertension.The CREST syndrome consists of calcinosis of the skin, Raynaud's phenomenon, sclerodactyly, telangiectasis and oesophageal dysmotility.This case describes a 48-year-old woman with known scleroderma demonstrating some of the less common radiological features.


1984 ◽  
Vol 77 (3) ◽  
pp. 489-496 ◽  
Author(s):  
William P. Follansbee ◽  
Edward I. Curtiss ◽  
Thomas A. Medsger ◽  
Gregory R. Owens ◽  
Virginia D. Steen ◽  
...  

1984 ◽  
Vol 310 (3) ◽  
pp. 142-148 ◽  
Author(s):  
William P. Follansbee ◽  
Edward I. Curtiss ◽  
Thomas A. Medsger ◽  
Virginia D. Steen ◽  
Barry F. Uretsky ◽  
...  

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