Image diagnoses for "Leg/Foot"
410 results with 1189 images

nevus melanocytic acral: completely sympotmless, congenital melanocytic, nevus that covers the sole and back of the foot. bizarre lateral borders, different shades of brown and black. six-monthly controls are indicated.

Teleangiectasia syndrome naevoides: A blurred redness of finest telangiectasia on the lower leg and foot of a 44-year-old woman that has existed for many years; the white part shows a naevus anaemicus (a frequent syndromal coupling).

Teleangiectasia syndrome naevoides: A blurred redness of finest telangiectasia on the lower leg and foot of a 44-year-old woman that has existed for many years.

Purpura eczematide-like purpura: non-symptomatic (no itching) eczema-like disease that has been recurrent for months in a completely healthy patient (no history of medication).

Purpura eczematid-like Purpura: explanatory detail.

Purpura eczematide-like purpura: non-symptomatic (no itching) eczema-like disease that has been recurrent for months in a completely healthy patient (no history of medication).

Purpura eczematide-like purpura: non-symptomatic (no itching) "eczema-like" disease that has been recurrent for months in a completely healthy patient (no history of medication).

Purpura eczematid-like Purpura: explanatory detail.

Scabies: chronic (existing for months) generalized, "eczematous" enormous, especially nightly itchy disease pattern with duct-like configured, rough papules.

vasculitis, leukocytoclastic (non-IgA-associated). multiple, acute, symmetric, localized on both legs for 2 weeks, symptomless, red, smooth spots and plaques. localized aspect of erythema multiforme.

Vasculitis, leukocytoclastic (non-IgA-associated). multiple, acute, symmetric, since 2 weeks existing, localized on both lower legs, irregularly distributed, 0.1-0.2 cm large, sharply defined, symptomless, hemorrhagic spots and blisters as well as beginning incrustations.

Erythema induratum (Nodular vasculitis): The 48-year-old patient has been suffering for 2 years from these intermittent, moderately painful, therapy-resistant plaques which tend to ulceration.

Scleroderma circumscripts (type band-shaped circumscripts scleroderma). 32-year-old woman, for years progressive symptoms. no significant symptoms. no restrictions in mobility.

Secondary lymphedema: chronic venous insufficiency with pronounced secondary lymphedema.

Varicosis: non-symptomatic trunk varicosis of the V. saphena magna.

Typical collar formation in the joint regions in lipedema, in this case also incipient secondary lymphedema with swelling of the back of the foot.

Acute contact allergic eczema: typical of the allergic pathogenesis of eczema is the blurred, scattered limitation of the inflammatory zone.

Erythema nodosum: acute, extensive painful indurated plaque.

Erythema nodosum: acute, multiple painful indurated plaques and nodules, accompanied by arthritis of the right ankle.

Erythema infectiosum: partly anular partly reticular erythema on the lower extremity.

Severe large bullous erysipelas

Largeulcer of the left lower leg and back of the foot in a 63-year-old female patient with CVI known for 20 years after several split skin transplants.

Large circumferentialulcer of the lower leg and back of the foot in a patient with CVI after several split skin transplants.

Granuloma anulare erythematous type. little indurated, marginal reddish-brown plaque with indicated central atrophy. slow centrifugal growth lasting for months. Granulomatosis disciformis chronica et progressiva is to be considered as a differential diagnosis (entity).

Klippel-Trénaunay syndrome: extensive, bilateral vascular malformation of capillary (naevus flammeus) and venous vessels (varicosis with chronic venous insufficiency - CVI); distinct soft tissue hypertrophy on the left side; no pelvic obliquity!