Image diagnoses for "Plaque (raised surface > 1cm)", "red"
433 results with 1902 images

lupus erythematodes chronicus discoides: 35-year-old otherwise healthy patient. skin lesions since 12 months, gradually increasing, no photosensitivity. multiple, chronically stationary, touch-sensitive, red, plaques with central adherent scaling. histology and DIF are typical for erythematodes. ANA and ENA were negative.

Psoriasis intertriginosa: inversely localised psoriasis with sharply defined red plaques and firmly adhering, shield-like scaly deposits.

Remark: in this case systemic therapy with fumaric acid ester is recommended.

Mycosis fungoides: tumor stage. 53-year-old man with multiple, disseminated, 1.0-5.0 cm large, in places also large, moderately itchy, clearly consistency increased, red, rough plaques.

Psoriasis seborrheic type: Psoriasis with little sharply defined, flat, barely elevated, therapy-resistant, scaly plaques.

Cellulitis, eosinophilic. early phase: Clear pruritus and dolent burning for several days. The differently sized erythema and rich red smooth plaques shown here have existed for 2 days.

ILVEN: Acquired psoriasiform blaschko-linear inflammatory dermatosis, partly flat and partly linearly arranged, moderate itching.

Acute allergic contact dermatitis: acute recurrence (1 year later) after re-dyeing of the hair with a hair dye containing para-phenylenediamine.

Airborne Contact Dermatitis: Acute, massively itching and burning dermatitis, which is limited to the freely carried skin areas, the lower border only blurred (leaking eczema foci), a typical feature of contact allergic eczema.

Psoriasis palmaris et plantaris (plaque type): flat palmar erythema; striated keratotic plaques that are loyal to the site.

Churg-Strauss syndrome: encircled central granulomatous regression zone (see histological preparation 1); on the right side the progression zone is outlined (see histological preparation 2).

Airborne Contact Dermatitis: Acute, extensive, enormously itchy and burning dermatitis with irregular, extensive infestation of the exposed facial areas including the eyelids.

Systemic lupus erythematosus (late onset): characteristic "collagenosis hands" with variable blue-red and livid-red patches. 83-year-old patient with known (since several years proven) systemic lupus erythematosus.

Atopic dermatitis in infancy, therapy resistant eczema foci on both hands.

Mycosis fungoides patch stage: For the first time in the 39-year-old woman multiple, itchy, erythematous, brownish, partly scaly, partly confluent plaques appeared at the gluteal region during pregnancy and spread to the legs in the course of the pregnancy. transition from parapsoriasis en plaques to mycosis fungoides in patch stage.

Erysipelas, acute: a sharply defined, flat, rich redness and swelling of the skin of the lower jaw, accompanied by painful regional lymphadenitis.

Necrobiosis lipoidica: Overview of the left thigh: Approx. 3 cm large, slightly elevated, erythematous plaque without ulcerations.

Intertrigo: 89-year-old woman, only slight obesity, but distinct hunchback.

Chronicdyskeratosis follicularis, also affecting the Rima ani (see detailed picture), intertriginous, whitish and red-brownish sooty, blurred, macerated, superficially rough, clearly increased in consistency, itchy and unpleasantly smelling plaques.

Tinea pedum (moccasin type). general view: For about 13 years non-healing redness and scaling, partly with severe itching, in the area of the right foot in a 30-year-old female patient. sharply defined, marginal scaling erythema, pustular formation, swelling of the foot with limited walking ability.