A Case of CREST Syndrome with Extensive Calcinosis Cutis.
- Author:
Hee Jeung KIM
1
;
Gun PARK
;
Hyo Chan JANG
;
Hyun CHUNG
Author Information
1. Department of Dermatology, The Catholic University of Daegu School of Medicine, Daegu, Korea. g9563009@cu.ac.kr
- Publication Type:Case Report
- Keywords:
Calcinosis cutis;
CREST syndrome
- MeSH:
Aged;
Calcinosis*;
CREST Syndrome*;
Esophageal Motility Disorders;
Female;
Fingers;
Humans;
Pelvis;
Scleroderma, Systemic;
Shoulder;
Telangiectasis
- From:Korean Journal of Dermatology
2006;44(9):1102-1105
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
CREST syndrome is an indolent form of systemic sclerosis and refers to the manifestations of calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly and telangiectasias. We report a typical case of CREST syndrome in a 67-year-old woman, who presented with extensive, hard, calcified nodules and plaques on her shins, fingers, pelvis, and shoulder.