Image diagnoses for "red"
899 results with 4541 images

dermatitis, seborrhoeic: 60-year-old patient with blanden own and family history of psoriasis. recurrent HV on the trunk for years. no itching. no evidence of dermatophytes. multiple, chronically inpatient, figured, borderline, non-itching, little scaling, clearly borderline, garland-shaped erythema.

Contact allergic dermatitis of the eyelids: chronic recurrent dermatitis with considerable and excruciating itching; recurrent morning swelling of the eyelids

Dermatofibroma, hemosiderin storing tumor on the lower leg of a 64-year-old female patient.

Eczema, hyperkeratotic-rhagadiform hand and foot eczema. chronic, polytopic, blurred, itchy, red, rough, partly scaly, partly crusty plaques with erosions and rhagades.

Chilblain lupus. early stage with livid-red, smooth, painful plaques. clinical picture reminiscent of chilblain (frostbite lupus). acrocyanosis still moderately pronounced.

Pemphigus vulgaris: 63-year-old patient with a pemphigus vulgaris (mucocutaneous type) that has existed for 3 years; extensive painful erosions of the capillitium.

Collagenosis, reactive perforating. detail enlargement: solitary, 0.3-1.3 cm large, red papules with a coarse central horn plug. the smaller papules correspond to an early stage of the disease.

Dimorphic leprosy of the lepromatous type: borderline leprosy of the lepromatous type with multiple, large, plate-like, borderline inflammatory lesions (type I leprosy reaction).

Erythema multiforme: suddenly occurring, itchy, disseminated exanthema with cocard-like plaques, which has been present for a few days; the skin lesions appeared shortly after starting antibiotic therapy for urinary tract infection.

Lichen planus verrucosus: Plaques on the left lower leg that have been unchanged for years and are very itchy (see scratching effects), with a red-violet seam in the marginal parts of the plaques.

psoriasis vulgaris. psoriasis guttata. general view: several, chronically inpatient, on the back disseminated, partly confluent, erythematous, silvery scaly papules and plaques of a 6-year-old boy. the skin changes had been conspicuous for the first time 6 months ago.

Impetigo contagiosa: multiple, artificially maintained, weeping and crusty plaques.

Desiccation dermatitis: Characteristic craquelée pattern with the diamond-shaped demarcation of the skin, the line pattern is created by the linear breaking up of the skin.

Acne fulminans: for months, known Acne vulgaris; now for several months intermittent febrile occurrence of rapidly melting, painful pustules Laboratory: inflammation parameters significantly increased, neutrophil leukocytosis (>10.000/ul)

Angiokeratoma scroti (detail): Chronically stationary, multiple, disseminated but also grouped (circle) bluish to dark black, smallest (arrows)0.2-0.5 cm large, smooth symptomless vesicles; star: slightly eroded vesicle.

Eczema atopic (overview): severe, universal (erythrodermic) atopic eczema. exacerbation phase since about 3 months. patient with rhinitis and conjunctivitis with pollinosis. total IgE >1.000IU.

Condition 4 weeks after germ removal, extensive removal of the underlying fibrosis plates by means of shave excision and defect coverage by means of split skin.

Systemic lupus erythematosus: after exposure to sunlight the findings worsen significantly with persistent, moderately sharply defined, symmetrical, non-scaling red plaques.

Typical - butterfly pattern - with a free perioral triangle. Bridge of nose, upper eyelids and tip of chin are affected.

Raynaud's phenomenon; disturbance of the general condition with arthralgia, fever up to 38°C.