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Abstract
Eosinophilic fasciitis (EF), also called Shulman's syndrome or fasciitis-panniculitis syndrome, is an uncommon scleroderma-like disorder of unknown etiology, characterized by induration and thickening of skin and soft tissue, usually associated with peripheral eosinophilia. In childhood, EF is poorly characterized.
Highlights
Eosinophilic fasciitis (EF), called Shulman’s syndrome or fasciitis-panniculitis syndrome, is an uncommon scleroderma-like disorder of unknown etiology, characterized by induration and thickening of skin and soft tissue, usually associated with peripheral eosinophilia
A case series of all patients diagnosed with EF at our Department
complete data were available for 16 pediatric cases
Summary
Eosinophilic fasciitis (EF), called Shulman’s syndrome or fasciitis-panniculitis syndrome, is an uncommon scleroderma-like disorder of unknown etiology, characterized by induration and thickening of skin and soft tissue, usually associated with peripheral eosinophilia.
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