TableĀ 3.
Clinical and Histopathologic Correlative Characteristics
| Patient | Disease | Time Since Sclerosis | Degree of Infiltrate | Prednisone | Transcriptomic Group |
|---|---|---|---|---|---|
| U1 | Unaffected | None | Unaffected | Yes | Unaffected |
| U2 | Unaffected | None | Unaffected | Yes | Unaffected |
| U3 | Unaffected | None | Unaffected | Yes | Unaffected |
| U4 | Unaffected | None | Unaffected | Yes | Unaffected |
| U5 | Unaffected | None | Unaffected | No | Unaffected |
| U6 | Unaffected | None | Unaffected | No | Unaffected |
| U7 | Unaffected | None | Unaffected | Yes | Unaffected |
| U8 | Unaffected | None | Unaffected | No | Unaffected |
| U9 | Unaffected | None | Unaffected | No | Unaffected |
| A1 | Affected | Late | Mild | Yes | 1 (fibrotic) |
| A2 | Affected | Early | Moderate | No | 5 (fibroinflammatory) |
| A3 | Affected | Late | Mild | Yes | 1 (fibrotic) |
| A4 | Affected | Early | Moderate | Yes | 4 (fibroinflammatory) |
| A5 | Affected | Late | Mild | Yes | ungrouped |
| A6 | Affected | Late | Mild | Yes | 3 (fibroinflammatory) |
| A7 | Affected | Late | Mild | No | 3 (fibroinflammatory) |
| A8 | Affected | Early | Mild | Yes | 1 (fibrotic) |
| A9 | Affected | Late | Mild | Yes | 1 (fibrotic) |
| A10 | Affected | Early | Mild | Yes | 2 (fibroinflammatory) |
| A11 | Affected | Early | Mild | Yes | 2 (fibroinflammatory) |
| A12 | Affected | Late | Mild | Yes | 4 (fibroinflammatory) |
| A13 | Affected | Early | Moderate | No | 5 (fibroinflammatory) |
| A14 | Affected | Early | Mild | Yes | 2 (fibroinflammatory) |
| A15 | Affected | Late | Moderate | Yes | 1 (fibrotic) |
| A16 | Affected | Early | Moderate | No | 5 (fibroinflammatory) |
| A17 | Affected | Early | Mild | Yes | 3 (fibroinflammatory) |
Abbreviations: A, affected; U, unaffected.
The term Early indicates <1 year since sclerosis onset; Late indicates >1 year. For the degree of infiltrate, mild indicates scattered immune cells either in a perivascular or interface pattern and moderate indicates a moderate inflammatory cell infiltrate in the dermis and/or a combination of a perivascular and interface inflammatory cell infiltrate. For prednisone, current use is described.