Concurrent linear scleroderma and systemic lupus erythematosus: a report of two cases. J Invest Dermatol 1979 Nov;73(5):368-72
Date
11/01/1979Pubmed ID
315439DOI
10.1111/1523-1747.ep12550429Scopus ID
2-s2.0-0018612979 (requires institutional sign-in at Scopus site) 35 CitationsAbstract
Two patients with linear scleroderma (en coup de sabre) developed systemic lupus erythematosus (SLE). This association has been well documented in only one previous case. The presence of high titer antibodies to ribonucleoprotein (RNP) initially led to the diagnosis of the mixed connective tissue disease. Development of more serious clinical involvement and antibodies to Sm (case 1) or native deoxyribonucleic acid (nDNA) (case 2) helped establish a diagnosis of SLE. Use of these studies in the differential diagnosis of systemic rheumatic diseases is disucssed briefly. The presence of anti-RNAP antibodies in patients with localized scleroderma may herald a more serious rheumatic disease.
Author List
Mackel SE, Kozin F, Ryan LM, Sheth KJ, Jordon REAuthor
Lawrence M. Ryan MD Emeritus Professor in the Medicine department at Medical College of WisconsinMESH terms used to index this publication - Major topics in bold
AdultAntibodies, Antinuclear
Biopsy
Child
Diagnosis, Differential
Female
Humans
Lupus Erythematosus, Systemic
Mixed Connective Tissue Disease
Ribonucleoproteins
Scleroderma, Systemic









