Presents with annular, erythematous plaques with a characteristic 'trailing scale' on the inner border, and is not associated with photosensitivity or autoantibodies.
Annular plaques of skin-colored papules, typically on the hands and feet, which are firm and lack the scale or photosensitivity of SCLE.
An autoimmune blistering disease with superficial, crusted erosions in a seborrheic distribution, caused by autoantibodies to desmoglein 1.
A pruritic papular or eczematous eruption that occurs hours to days after sun exposure and resolves completely, unlike the more persistent lesions of SCLE.
Presents as urticarial, eczematous, or annular plaques that are intensely pruritic and precede the formation of tense bullae.
Presents with well-demarcated, erythematous plaques with a thick, silvery scale, a different morphology from the annular or papulosquamous lesions of SCLE.
Confined to the central face, with papules, pustules, and telangiectasias, but lacks the annular plaques and positive Ro/SSA antibodies of SCLE.
Can present with annular lesions, but they are typically composed of firm, reddish-brown papules and biopsy shows non-caseating granulomas.
An annular fungal infection with a raised, scaly, active border that can be confirmed with a KOH preparation.
Presents as transient, pruritic wheals that last for hours, not the persistent, photosensitive plaques of SCLE.