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Systemic scleroderma and perforating granuloma annulare: differential diagnosis from calcinosis
Abstract
Background:
Systemic scleroderma is a disorder of unknown etiology with skin sclerosis. Its major histological features are swollen and homogenized collagen bundles.
Objective And Methods:
We describe 2 patients with systemic sclerosis who have multiple umbilicated nodules indistinguishable from calcinosis cutis.
Results:
Histological examinations including Von Kossa staining revealed features of perforating granuloma annulare, but not of calcinosis cutis.
Conclusion:
The association may not be fortuitous but both diseases may be etiologically related.