Document Detail


The 'CREST' syndrome. Comparison with systemic sclerosis (scleroderma).
MedLine Citation:
PMID:  508020     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The CREST syndrome refers to a disorder comprising the manifestations of calcinosis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, and telangiectasia. Thirteen CREST patients (two with CRST) were compared with 26 patients with systemic sclerosis but without the full manifestations of the CRST syndrome. No significant difference was found between the groups in the age of onset of Raynaud's phenomenon, degree of multiphasic digital color changes, ulcerations of fingers, sclerodactyly, or in the frequency of abnormal esophageal peristalsis or dysphagia. Laboratory results were similar, including the frequency of an elevated ESR. However, the CREST patients had a significantly lower frequency of arthralgia (54%) and arthritis (15%) than did those with scleroderma (88% and 65%, respectively). All but one of the CREST patients were women, which was a greater proportion than found among scleroderma cases (69%), and all were white (P less than .05). Most patients with the CREST syndrome had rather severe acrosclerosis. At last evaluation, four patients were chronically ill and three had died. The CREST and CRST syndromes are closely related disorders that seem to be part of the spectrum of systemic sclerosis.
Authors:
E E Velayos; A T Masi; M B Stevens; L E Shulman
Publication Detail:
Type:  Case Reports; Comparative Study; Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Archives of internal medicine     Volume:  139     ISSN:  0003-9926     ISO Abbreviation:  Arch. Intern. Med.     Publication Date:  1979 Nov 
Date Detail:
Created Date:  1980-01-28     Completed Date:  1980-01-28     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0372440     Medline TA:  Arch Intern Med     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  1240-4     Citation Subset:  AIM; IM    
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MeSH Terms
Descriptor/Qualifier:
Adult
Calcinosis / diagnosis*
Diagnosis, Differential
Esophageal Diseases / diagnosis*
Female
Fingers*
Humans
Middle Aged
Raynaud Disease / diagnosis*
Scleroderma, Systemic / diagnosis*
Syndrome
Telangiectasis / diagnosis*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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