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The fascia in systemic scleroderma
Journal of the American Academy of Dermatology
|July 1, 1980
Summary
Diffuse fasciitis and systemic scleroderma share fascial involvement. Deep fascia biopsies in systemic scleroderma patients revealed thickening and fibrosis, indicating this is not unique to diffuse fasciitis.
Area of Science:
- Rheumatology
- Dermatology
- Pathology
Background:
- Diffuse fasciitis (DF) and systemic scleroderma (SS) exhibit overlapping clinical and pathological characteristics.
- Deep fascial involvement is considered a hallmark of DF, but its presence in SS is less understood.
Purpose of the Study:
- To investigate the occurrence and characteristics of fascial involvement in patients diagnosed with systemic scleroderma.
- To determine if fascial changes are a distinctive feature of DF or if they are also present in SS.
Main Methods:
- Deep fascial biopsies were obtained from ten patients diagnosed with systemic scleroderma.
- Histopathological examination of the fascia was performed to identify changes such as thickening and fibrosis.
Main Results:
- All systemic scleroderma patients displayed typical dermal histological findings consistent with scleroderma.
- Five out of ten systemic scleroderma patients showed evidence of fascial thickening and fibrosis in the deep fascia biopsies.
- These findings suggest that fascial involvement is not exclusive to DF.
Conclusions:
- Fascial involvement, including thickening and fibrosis, is not a unique pathological feature of diffuse fasciitis.
- Systemic scleroderma can also present with significant involvement of the deep fascia.
- Fascial thickening represents a shared morphologic characteristic between diffuse fasciitis and systemic scleroderma.