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

Lymphomatoid papulosis: chronic, relapsing, completely asymptomatic clinical picture with multiple, 0.3 - 1.2 cm large, flat, scaly papules and nodules and ulcers.

Lymphomatoid papulosis: intermittent, painless, papules and nodules with central necrosis and crust formation (nodules above).

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.

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.

Klippel-Trénaunay syndrome: extensive vascular malformation with extensive nevus flammeus affecting the trunk, the right arm and both legs. No evidence of soft tissue hypertrophy so far. No AV fistulas.

Nummular dermatitis (nummular/microbial eczema): chronically active, itchy, brownish-greyish, flat raised, partly eroded, partly crusty plaques in a 54-year-old man, excised for 8 weeks.

Nummular dermatitis ( nummular/microbial eczema): Chronically active, 8-week-old, approx. 8 cm tall, brownish, raised, partly eroded, partly crusty, solid, considerably itchy plaque in a 47-year-old man.

Scleroderma ligamentous: for years slowly progressive, only moderately indurated ligamentous morphea in a 42-year-old woman; no movement restrictions of the joints.

Scleroderma ligamentous: for years slowly progressive, only moderately indurated ligamentous morphea in a 42-year-old woman; no movement restrictions of the joints.

Scleroderma ligamentous: for years slowly progressive, only moderately indurated ligamentous morphea in a 42-year-old woman; no movement restrictions of the joints; follicular structures within the lesions no longer detectable (inlet: mutual area with distinct keratosis follicularis).

Psoriasis vulgaris chronic active plaque type: relapsing activity after angina tonsillaris, partly larger plaques and disseminated papules.

Mycosis fungoides follikulotrope: generalised clinical picture; smooth plaques that dissect at the edges, with clear follicular involvement. Moderate itching.

Folliculotropic Mycosis fungoides: generalized picture of the disease with smooth plaques that dissect at the edges, where the follicle-relatedness is clearly recognizable.

Pronounced livedo racemosa: Intermediate findings after 2 more years (period of clinical follow-up over a period of 8 years); extensive scar healing after therapy with high-dose venous immunoglobulin therapy (IVIG)

Pronounced livedo racemosa: Intermediate findings after 2 more years (period of clinical follow-up over a period of 8 years); few lesions with very painful central necroses.

Pronounced livedo racemosa: interim findings 2 years later (period of clinical follow-up over a period of 8 years).

Pronounced livedo racemosa: with a clinical course over 8 years. Extremely painful red, reticular plaques, especially at temperature change, in a 43-year-old, otherwise healthy patient. Initial findings.

Cholesterol embolism: passionate 73-year-old smoker with pronounced livdeo reticularis and extremely painful, "overnight", poorly healing ulcers on knee and lower leg.

Livedo racemosa : irregular, bizarre non-closed circle segments, as pioneering morphological indicators of livedo racemosa, and cholesterol embolism occurred in this 73-year-old passon smoker.

Lymphoma, cutaneous diffuse large-cell B-cell lymphoma leg type: Approx. 10-12 cm diameter, irregularly shaped, deep red tumor with a smooth surface, in a 69-year-old patient.

Aggressive cytotoxic epidermotropic CD8-positive T-cell lymphoma: generalized, rapidly spreading red itchy plaques; retracted scars after formation of ulcerated, deep-seated nodules.

Nummular dermatitis (eczema, microbial): Itchy, scaly, coin-shaped plaques on the lower leg that have persisted for several months.

Cholesterol embolism: Patient with recurrent, suddenly occurring, very painful, therapy-resistant ulcers; moderately pronounced livedo image.

melanoma malignes amelanotic: since earliest childhood a pigment mark is known at this site. continuous growth for several years. ulceration of the node for half a year. no significant symptoms. the diagnosis cannot be made on the basis of the clinical picture.