Image diagnoses for "Macule", "red", "Leg/Foot"
48 results with 128 images

Chilblain lupus - detailed view

Purpura eczematid-like Purpura: explanatory detail.

Naevus flammeus: congenital, bilateral, chronically inpatient, bizarre, asymptomatic, non-syndromal naevus flammeus with livedo-like aspect

Spider veins, reflected light microscopy

Nevus flammeus: congenital, asymmetrically arranged, non-syndromal (no tissue hypertrophy, no orthopedic malposition) large-area (telangiectatic) vascular nevus; characteristic are the scattered borders of the red spots.

Chilblain lupus - temperature dependent redness, swelling and painfulness of several toes.

Purpura thrombocytopenic: colorful picture of an orthostatic purpura with fresh, punctiform, red bleeding.

acrodermatitis chronica atrophicans: 69-year-old woman. for 4 months right lower leg flat livid-red. at the beginning somewhat edematous. not overheated. subjectively symptomless except for slight hyperesthesia lateral foot edge on the right. no improvement by elevation. no tick bite recallable. in the laboratory confirmation of Lyme disease (high titer IgG, low titer IgM). no further manifestations except ACA.

Mononucleosis, infectious. increased confluence of macular and urticarial erythema in the foot area.

Erythema infectiosum: generalized exanthema with larger and smaller, in its complete manifestation about 3.0 cm in diameter, less symptomatic, on the surface slightly roughened, anular erythema.

Dermatitis, phototoxic. about 48 hours old, distally (by socks) sharply bordered, severely itching, partly erythematous, partly vesicular or bullous dermatitis. the 45-year-old patient had applied a St. John's wort containing liquid to the lower leg during a picnic in the countryside because of an insect bite. the same evening the first inflammatory skin symptoms appeared.

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.

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.

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.

Purpura thrombocytopenic: acutely occurring, partly large-area, partly punctiform, non-anemic spots with a tendency to confluence; sudden onset with fever, multiple thromboses, disorientation, stupor; it is a drug-induced form of thrombotic thrombocytopenic purpura with hemolytic microangiopathic anemia at the base of an infectious disease and a previously unknown drug allergy.

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.

erysipelas. extensive redness and swelling of the left foot in a 71-year-old man. on the left back of the foot there is a sharply limited overheated erythema with flame-like runners of 15 x 15 cm in size. the back of the foot is circumferentially enlarged and painful. secondary findings are the palpation of single, enlarged, pressure-dolent lymph nodes in the corresponding lymph drainage area of the groin region.

Teleangiectasia. Dense network of vasodilatation, distal sharp recess.

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