
Drug exanthema maculo-papular L27.0
Drug exanthema after taking a cephalosporin. 4 days after continuous intake of the antibiotic sudden (overnight) development of this moderately itchy, maculo-papular exanthema.

Adult dermatomyositis M33.1
Dermatomyositis; acutely occurring, succulent exanthema, massive itching with scratching effects; general fatigue,

Mixed connective tissue disease M35.10
Mixed connective tissue disease: 43-year-old female patient (with clinical aspect of systemic lupus erythematosus) who fulfils the criteria of MCTD: U1.nRNP : titre : >1:1600; characteristics of systemic lupus erythematosus, Raynaud's phenomenon, swollen hands as well as feeling ill, fatigue, proximal muscle weakness (typical myositis symptoms).

Klippel-trénaunay syndrome Q87.2
Klippel-Trénaunay syndrome: extensive vascular malformation with extensive nevus flammeus affecting the trunk and both arms. So far no evidence of soft tissue hypertrophy. No AV fistulas.

Atopic anal dermatitis L20.8
Eczema, anal eczema, atopic dermatitis, chronic ekezmatouschanges of the perianal region with known atopic diathesis.

Erythema perstans faciei L53.83
erythema perstans faciei: symmetric, reddening of both cheeks. is not considered a clinical picture by the patient. furthermore signs of a distinct keratosis pilaris on both upper arms.

Dermatomyositis (overview) M33.-
dermatomyositis. chronic stationary, flat, red, "heliotropic" exanthema. typical pronounced periorbital paleness. general fatigue, muscle weakness.

Ecchymosis syndrome, painful R23.8
ecchymosis syndrome, painful. intermittent manifestation of painful, demonstrably non-traumatic induced skin bleeding in a 61-year-old woman. initial pressure-sensitive erythema. subsequent development of skin bleeding and slow expansion of the skin changes. chronic recurrent course. no underlying disease known.

Interstitial granulomatous dermatitis with plaques L92.1

Striae cutis distensae L90.6

Atopic photoaggravated dermatitis L20.8
Eczema atopic photoaggravated: 72-year-old female patient with a known, less active, chronic atopic eczema. 1 year ago the patient noticed an increasing "sensitivity to light". The present UV-triggered exacerbation with pronounced itching (after a long walk in summer sunshine) has persisted for 3 months. Despite local treatment with a class II steroid externum it proved to be resistant to therapy.

Teleangiectasia I78.8
Teleangidectasia: irregular caliber, in places ectatic capillaries in a nodular basal cell carcinoma.

Vasculitis (overview) L95.8

Perioral dermatitis L71.0

Klippel-trénaunay syndrome Q87.2
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.

Ulerythema ophryogenes L66.4
Ulerythema ophryogenes: the area marked by the square shows follicular papules (keratosis follicularis) on an enlarged scale with a reddened courtyard which merges into a two-dimensional erythema.

Klippel-trénaunay syndrome Q87.2
Klippel-Trénaunay syndrome: Extensive vascular malformation with a large-area nevus flammeus affecting the trunk and the right lower extremity with soft tissue hypertrophy of the right lower extremity; pelvic obliquity.

Livedo racemosa (overview) M30.8
Livedo racemosa:generalized livedo racemosa with characteristic bizarre reddening of the skin, which typically does not form closed ring structures; no other organ alterations