
A case of CREST syndrome (calcinosis, Raynaud's phenomenon, esophageal hypomotility, sclerodactyly, and telangiectasia) that initially showed Raynaud's phenomenon, sclerodactyly and polyarthralgias, 3 years later completing the process, associated to sicca syndrome, is presented. The esophageal affectation showed a loss of peristalsis of the inferior 2/3, as well as hypotonia of the gastroesophageal sphincter. We comment the prognostic relationship between CREST syndrome and the centromeric region antibodies.
Scleroderma, Systemic, Centromere, Calcinosis, Raynaud Disease, Syndrome, Middle Aged, Esophageal Diseases, Prognosis, Antibodies, Sjogren's Syndrome, Humans, Female, Telangiectasis
Scleroderma, Systemic, Centromere, Calcinosis, Raynaud Disease, Syndrome, Middle Aged, Esophageal Diseases, Prognosis, Antibodies, Sjogren's Syndrome, Humans, Female, Telangiectasis
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