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In vivo study of scleroderma by non-invasive techniques
B Kalis1, J De Rigal, F Léonard
1Département de Dermatologie, Hôpital Sébastopol, Reims, France.
The British Journal of Dermatology
|June 1, 1990
Summary
Localized scleroderma (LS) and progressive systemic sclerosis (PSS) show decreased skin extensibility and increased skin thickness. These skin changes, along with microcirculation differences in LS, help track disease progression.
Area of Science:
- Dermatology
- Rheumatology
- Medical Physiology
Background:
- Scleroderma encompasses localized scleroderma (LS) and progressive systemic sclerosis (PSS), both characterized by skin hardening.
- Understanding the distinct pathophysiological changes in the skin of LS and PSS is crucial for effective disease management.
Purpose of the Study:
- To investigate and compare skin thickness, extensibility, transcutaneous oxygen tension (PO2), and cutaneous blood flow in patients with LS and PSS versus healthy controls.
- To identify key non-invasive parameters for monitoring the progression of LS and PSS.
Main Methods:
- Non-invasive techniques were employed to assess skin properties and microcirculation.
- Measurements included skin thickness, skin extensibility, transcutaneous PO2, and cutaneous blood flow.
- Data from 16 LS patients, 11 PSS patients, and normal controls were analyzed.
Main Results:
- Localized scleroderma (LS) exhibited decreased skin extensibility and thickened skin in progressive lesions, alongside increased cutaneous microcirculation and decreased transcutaneous PO2.
- Progressive systemic sclerosis (PSS) showed reduced skin extensibility due to skin thickening, but no significant alterations in cutaneous microcirculation or PO2.
- Skin thickness and extensibility emerged as significant indicators differentiating the conditions.
Conclusions:
- Skin thickness and extensibility are highly valuable non-invasive parameters for assessing the progression of both localized scleroderma and progressive systemic sclerosis.
- Distinct alterations in cutaneous microcirculation and oxygenation are observed in LS but not in PSS, suggesting different underlying mechanisms.