Linear Morphea en Coup de Sabre, a Rare Subtype of Localized Scleroderma
Nissrine Amraoui
Abstract
Nissrine Amraoui
Abstract
Scleroderma is a rare connective tissue disease that is manifested by cutaneous sclerosis and variable systemic involvement [1]. Two categories of scleroderma are known: systemic sclerosis (SSc), characterized by cutaneous sclerosis and visceral involvement, and localized scleroderma (LoS) or morphea which is confined to the skin and/or underlying tissues [1,2].
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Scleroderma is a rare connective tissue disease that is manifested by cutaneous sclerosis and variable systemic involvement [1]. Two categories of scleroderma are known: systemic sclerosis (SSc), characterized by cutaneous sclerosis and visceral involvement, and localized scleroderma (LoS) or morphea which is confined to the skin and/or underlying tissues [1,2].
Key concepts: Morphea, Scleroderma (fungus), Localized Scleroderma, Medicine, Connective tissue disease, Connective Tissue Disorder, Dermatology, Pathology