Table 3 . Association between different scleroderma patterns and clinical or laboratory features .
Features | Scleroderma pattern | ||||
Early pattern n (%) | Active pattern n (%) | Late pattern n (%) | Non-specific pattern n (%) | p | |
Symptoms and signs, % |
|||||
Fever | 1(16.7%) | 3(50%) | 1(16.7%) | 1(16.7%) | 0.20 |
Heliotrope rash | 0 | 6(50%) | 4(33.3%) | 2(16.7%) | 1 |
Gottron papules | 1(4.3%) | 8(34.8%) | 11(47.8%) | 3(13%) | 1 |
Gottron's sign | 0 | 8(42.1%) | 10(52.6%) | 1(5.3%) | 0.56 |
V sign | 1(4.3%) | 2(28.6%) | 3(42.9%) | 1(14.3%) | 0.76 |
Shawl sign | 0 | 2(66.7%) | 1(33.3%) | 0 | 0.41 |
Preorbital edema | 1(16.7%) | 2(33.3%) | 2(33.3%) | 1(16.7%) | 0.53 |
Calcification | 0 | 5(50%) | 4(40%) | 1(10%) | 0.60 |
Mechanic hand | 1(8.3%) | 4(33.3%) | 6(50%) | 1(8.3%) | 0.60 |
Facial erythema | 1(16.7%) | 7(46.7%) | 6(40%) | 1(6.7%) | 0.06 |
Arthritis | 1(25%) | 1(25%) | 1(25%) | 1(25%) | 0.71 |
Polyarthralgia | 1(16.7%) | 7(46.7%) | 6(40%) | 1(6.7%) | 0.06 |
ILD* | 0 | 3(33.3%) | 4(44.4%) | 2(22.2%) | 0.41 |
Dysphasia | 0 | 3(37.5%) | 4(50%) | 1(12.5%) | 1 |
Muscle weakness | 0 | 9(45%) | 9(45%) | 2(10%) | 0.56 |
Laboratory findings, % | |||||
CK† | 25% | 17.9% | 7.1% | 50% | 0.29 |
ESR‡ | 1(5.5%) | 8(44.5%) | 7(38.9%) | 2(11.1%) | 0.16 |
CRP§ | 0 | 2(40%) | 2(40%) | 1(20%) | 1 |
ANA|| | 1(7.7%) | 5(38.5%) | 7(53.8%) | 0 | 0.11 |
Anti RO antibody | 0 | 0 | 4(100%) | 0 | 0.46 |
Anti JO1 antibody | 0 | 2(50%) | 2(50%) | 0 | 0.71 |
Myopathic EMG¶ | 1(5.3%) | 9(47.3%) | 8(42.1%) | 1(5.3%) | 0.015 |
*ILD: Interstitial lung disease, †CK: creatine kinase, ‡ESR: Erythrocyte sedimentation rate. A level of >12 in male and >18 in female was considered abnormal [52]. §CRP: C-Reactive Protein. A level of >5 mg/L was considered as abnormal.
||ANA: Antinuclear antibody, ¶EMG: electromyography