Image diagnoses for "red"
876 results with 4456 images

Dermatomyositis; acutely occurring, succulent exanthema, massive itching with scratching effects; general fatigue,

Zoster generalisatus (with drug-induced immunosuppression): For 5 days increasing redness and swelling of the skin with stabbing, shooting pain. extensive erythema, blisters, scaly crusts and swelling. > 25 blisters beyond the segmental infestation.

Keratoakanthoma classic type: rarelocalization of a keratoakanthoma otherwise typical of the course (existing for 6 weeks) and clinical aspect

Lymphomatoid papulosis: Painless, flat papules and nodules with central scaling and crust formation, appearing intermittently for more than 1 year, 0.3 - 1.2 cm in size. 45-year-old otherwise healthy male.

Psoriasis: relapsing-active psoriasis with appearance of psoriatic lesions in "textile-covered" skin areas.

Sarcoidosis plaue-form: Slightly pressure-painful, livid, blurred plate-like indurations in the skin.

Atopic dermatitis: clinical picture of the so-called milk crust.

Folliculitis, gram-negative. in the area of the facial skin localized, disseminated standing, solitary, partly excised papules, pustules and nodules in a 50-year-old man. periorbital lichenification of the skin relief.

Lupus erythematosus chronicus: chronic, cutaneous lupus erythematosus with scaly touch-sensitive plaques; no ANA or DNA ac.

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).

Dermatosis, acute febrile neutrophilic. reddish-livid, succulent, pressure-dolent, infiltrated, solitary and partly confluent papules confluent to plaques, on the lower leg in a 33-year-old patient. 1 week before the onset of the disease a fever attack with temperatures > 38 °C occurred.

Pemphigus vulgaris: multiple, chronic, since 3 years intermittent formation of large, easily injured, flaccid, 0.2-3.0 cm large, red blisters, which have united here to form larger, blister lakes.

Dermatitis, seborrhoeic. 6-month-old female patient with almost symmetrical, blurred, flatly infiltrated, scaly, non-itching red plaques. good clinical response to steroidal pre-treatment. recurrence of skin symptoms within a few days after discontinuation of therapy.

Acne conglobata: healed state.

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.

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

Mycosis fungoides: Tumor stage. 53-year-old man with multiple, disseminated, 1.0-5.0 cm large, in places also large-area, moderately itchy, clearly consistency increased, red, rough, eroded plaques. development over 4 years.

Lymphoma cutaneous T-cell lymphoma panniculitis-like: circumscribed, rather inconspicuous, moderately painful, red, in places ulcerated and clearly indurated plaque.