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Preliminary criteria for the classification of systemic sclerosis (scleroderma)

Arthritis & Rheumatism · 1980 · Vol. 23(5) · pp. 581–590
Alfonse T. Masi

Abstract

A multicenter, ongoing study of early-diagnosed cases of systemic sclerosis and comparison patients with systemic lupus erythematosus, polymyositis/dermatomyositis, and Raynaud's phenomenon was conducted in order to develop classification criteria for systemic sclerosis. Preliminary criteria are proposed namely, the finding of either the sole major criterion, i.e., proximal scleroderma, or two or more of the minor criteria, i.e., 1) sclerodactyly, 2) digital pitting scars of fingertips or loss of substance of the distal finger pad, and 3) bilateral basilar pulmonary fibrosis. When applied to the case and comparison patients included in this study, these proposed criteria had a 97% sensitivity for definite systemic sclerosis and 98% specificity.

Systemic Sclerosis and Related DiseasesInflammatory Myopathies and DermatomyositisSkin Diseases and DiabetesMedicineScleroderma (fungus)SclerodactylyPolymyositisDermatomyositisSystemic sclerodermaSystemic diseaseDermatologyInternal medicinePathology

MeSH terms

AdolescentAdultAgedConnective TissueDiagnosis, DifferentialFemaleFollow-Up StudiesHumansMaleMiddle AgedRaynaud DiseaseScleroderma, SystemicSkin
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