Uncommon skeletal findings in systemic sclerosis (scleroderma)

SA Journal of Radiology

 
 
Field Value
 
Title Uncommon skeletal findings in systemic sclerosis (scleroderma)
 
Creator van der Walt, Betsie van de Werke, Irma Lockhat, Zarina
 
Subject — —
Description 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.
 
Publisher AOSIS
 
Contributor
Date 2002-03-31
 
Type info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion — —
Format application/pdf
Identifier 10.4102/sajr.v6i1.1458
 
Source South African Journal of Radiology; Vol 6, No 1 (2002); 28-32 2078-6778 1027-202X
 
Language eng
 
Relation
The following web links (URLs) may trigger a file download or direct you to an alternative webpage to gain access to a publication file format of the published article:

https://sajr.org.za/index.php/sajr/article/view/1458/1830
 
Coverage — — —
Rights Copyright (c) 2018 Betsie van der Walt, Irma van de Werke, Zarina Loekhat https://creativecommons.org/licenses/by/4.0
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