Larva migrans, detail: Garland-shaped, tortuous, erythematous, partly scaly plaque on the right foot back of a 35-year-old patient after a bathing holiday in Thailand.
herpes simplex virus infection. in a 30-year-old patient, there are grouped, itchy, slightly painful, yellow, smooth blisters with surrounding erythema in the area of the inner preputial leaf. previously, similar skin lesions had occurred three times. burning pain. the clinical picture is diagnostically conclusive
Scabies in a 3-year-old boy: since several months existing, massively itching, generalized clinical picture with disseminated scaly papules and plaques, here infestation of the palms.
Bowenoid papulosis. 32-year-old patient, anamnestic condylomata acuminata. After successful therapy within a period of 6 months development of these symptomless lesions. Findings: 0.2-0.5 cm large, firm papules with smooth surface.
acne inversa. detailed view of the chronically inpatient, painful, bulging and consistency increased skin changes. due to the chronic course, elongated, strand-like scars have already formed in the left axilla. secondary findings show an abscessed fistula duct.
Pemphigoid, bullous. 0.5-5.0 cm large, bulging, partly hemorrhagic blisters which are localized on two-dimensional, borderline erythema or plaques, on the right hand of an 81-year-old woman.
Mastocytosis diffuse of the skin: Disseminated large-area mastocytosis of the skin (type Ia). In addition to the conspicuous yellow-brown spots and plaques, the apparently unaffected skin is slushy thickened, in places also with protruding follicular structures. The occurrence of larger blisters after banal trauma has been reported time and again. No systemic involvement detectable.
Lichen (ruber) planus ulcerosus: extensive infestation of the feet with verrucous and crusty deposits and therapy-resistant deep ulcers with rough edges.
Systemic lupus erythematosus: changes in the oral mucosa with extensive erosions and veil-like whitish plaques; spicy and very warm food leads to considerable painful burning.
Klippel-Trénaunay syndrome: extensive vascular malformation with extensive nevus flammeus affecting the trunk and both arms with distinct soft tissue hypertrophy of the right arm.
Recurrent sterile pustular disease of theacromion, which tends to mutate and leads to atrophy and loss of nails if it occurs repeatedly and persists for a long time (see figure).
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