Myocardial function and perfusion in the CREST syndrome variant of progressive systemic sclerosis

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 77 (9) ◽  
pp. 793-794 ◽  
Author(s):  
S M Burge ◽  
T J Ryan ◽  
R P R Dawber

A case of progressive systemic sclerosis (CREST syndrome), which began in childhood, is described. Juvenile onset CREST syndrome is extremely rare; there are few well documented cases and no published series of children with this form of progressive systemic sclerosis. An anticentromere antibody was recently detected in this case and its significance is discussed.


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.


1991 ◽  
Vol 14 (4) ◽  
pp. 439-446 ◽  
Author(s):  
Kozo Onami ◽  
Yutaka Kikuta ◽  
Tomoe Nishimaki ◽  
Reiji Kasukawa

1986 ◽  
Vol 48 (4) ◽  
pp. 652-655
Author(s):  
Kouzou OOKAWA ◽  
Jiro ARATA ◽  
Jingo SATO

Sign in / Sign up

Export Citation Format

Share Document