Image diagnoses for "red"
893 results with 4522 images

Angiomatosis, bacillary enlargement, partly isolated, partly grouped hemorrhagic papules up to approx. 2 cm in size

Livedo racemosa: irregular, bizarre, not closed circular segments on the lower leg and ankle region, as pioneering morphological indicators of livedo racemosa; for several months, painful, bizarrely configured ulcer in the middle of the calf.

Lichen planus verrucosus. numerous, chronically stationary, 0.5-5.0 cm in size, rough, brownish or brownish-red, disseminated or confluent, rough, wart-like plaques as well as severe itching in a 63-year-old woman. onset of symptoms about 6-7 years ago. known CVI for 10 years.

Psoriasis intertriginosa: chronic, intertriginous focus with maceration in the rima ani. intermittent itching, especially after sweating or prolonged sitting. also formation of painful fissures.

Tinea pedum: Close-up; coarse lamellar scaling persisting for months with moderate itching.

Acute urticaria: Acute exanthema with multiple, disseminated red wheals, which in places flow together to form large areas, are flatly elevated and itchy.

Angiokeratoma circumscriptum. 20-year-old female patient with a lesion composed of several types of efflorescence. The skin lesions present have existed since birth. The blue-black parts have gradually developed over the past five years. In addition to two-dimensional red spots (upper part), red papules (lower part) and blue-black bumped plaques with a smooth, shiny surface are found. Soft, spongy consistency in the centre.

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).