Image diagnoses for "Macule"
332 results with 1231 images

Systemic lupus erythematosus: acute maculopapular exanthema, accompanied by recurrent fever attacks, fatigue and exhaustion, arthralgia, inflammation parameters +, ANA high titer positive, rheumatoid factor +, DNA-AK+. UV-relatedness of the exanthema is not detectable.

Hyperpigmentation, post-inflammatory. multiple, on both cheeks localized, chronically stationary, laminar, no longer increasing, circumscribed brown discoloration of the skin. Occurs following severe contact dermatitis with frequent use of cosmetics despite existing type 4 sensitization to fragrances.

Dermatitis contact allergic: extensive itching, blurredly limited erythema.

Vascular twin nevus: Combination of a nevus flammeus with a nevus anaemicus.

Mastocytosis diffuse of the skin: Disseminated large-area mastocytosis of the skin (type Ia); no systemic involvement detectable (detailed picture)

Erythronychia, localized longitudinal. idiopathic, solitary, painless, red longitudinal striation of the left thumbnail plate with a low-grade, V-shaped retraction and splinter hemorrhage in a 29-year-old female patient.

Teleangiectasia. Dense network of vasodilatation, distal sharp recess.

Nevus flammeus lateralis; chronic inpatient, bizarrely limited, symptomless, red, smooth spot on the right side of the face in a 12-year-old girl.

Becker-Naevus: chronically stationary, planar, splatter-like light brown pigmented, rough, sharply defined stain; no change in pigmentation in the last 20 months compared to the previous findings

Scleroderma, systemic: within 2-3 years, newly developed telangiectasia of the facial skin.

Naevus anaemicus. solitary, permanent, congenital, 1.0-10.0 cm large, bizarrely limited, symptomless, smooth, bright spot on the back of a 33-year-old man. rubbing causes the surrounding area to redden, the spot remains white.

Desiccation dermatitis: slight, pityriasiform scaling with a characteristic craquelée pattern with linear cracking

Erysipelas bullöses: acuteextensive, sharply defined, painful reddening and plaque with circumscribed large blisters; entry portal: tinea pedum.

Amyloidosis systemic: Flat light brown, symptomless plaques on both backs of the hands and fingers; recurrent fresh haemorrhages after banal traumas.