Abstract
Systemic sclerosis is one of the multiple cutaneous sclerosing disorders. The dermatoses that share the clinical morphology of systemic sclerosis are called scleroderma mimics. These include inflammatory and immune-mediated (eosinophilic fasciitis, chronic graft versus host disease, generalized morphea), metabolic (hypothyroidism, porphyria cutanea tarda), deposition (scleromyxedema, systemic amyloidosis, nephrogenic systemic fibrosis, scleredema), hereditary (congenital fascial dystrophy, progeroid disorders), and occupational and toxin-mediated disorders.
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