Image diagnoses for "Plaque (raised surface > 1cm)", "red"
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Results for Plaque (raised surface > 1cm) red
Mycosis fungoides plaque stage C84.0
Mycosis fungoides (plaque stage): 72-year-old male (so-called plaque stage of Mycosis fungoides); multiple, disseminated, 5.0-10.0 cm large, occasionally slightly itchy, only slightly consistency increased, slightly scaly red, poikilodermatic plaques are found.
Psoriasis palmaris et plantaris (plaque type) L40.3
Psoriasis palmaris et plantaris (plaquet type): For explanations see the following figure.
Lupus erythematodes chronicus discoides L93.0
Lupus erythematodes chronicus discoides: dry-scaling, red, hyperesthetic, plaques with adherent scaling that have existed on both halves of the face for 5 years; no evidence of systemic LE. DIF with typical pattern.
Atopic dermatitis (overview) L20.-
Eczema atopic (overview): severe atopic eczema existing for years, mainly localized in the adolescence, diffractive, generalized for 2 years now, massive constant itching, intensified after sweating, numerous scratch marks.
Gigantean condyloma A63.0
Condylomata gigantea. 39-year-old patient has had rapidly growing, perianal, localised, extensive papillomatous, sometimes nodular, superficially fissured vegetation for about 12 months. HPV typing revealed HPV types 6 and 18.
Pemphigus erythematosus L10.4
Pemphigus erythematosus. multiple, chronic, recurrent for 1 year, symmetrical, trunk-accentuated, red, rough plaques with coarse lamellar scales and crusts, preferably localized in seborrheic areas. little itching.
Lupus erythematosus (overview) L93.-
Lupus erythematosus (overview): systemic lupus erythematosus. numerous smaller, painful erosions and flat ulcers on the red of the lips. red plaques on the skin of the lips.
Epidermolysis bullosa junctionalis generalized intermediaries (non-herlitz) Q81.1
Epidermolysis bullosa dystrophica dominans: 35-year-old female patient, with extensive scarring blister formation after banal traumas (e.g. under plasters, or under pressure). First manifestation in the first months of life. recurrent formation of basal cell carcinomas.
Balanitis plasmacellularis N48.1
Plasmacellular vulvitis. Analogous findings in female genitals. Symmetrical contact patch.
Intertriginous psoriasis L40.84
Psoriasis intertriginosa: infection-induced, acute (intertriginously accentuated) relapsing activity of a long-term pre-existing psoriasis vulgaris.
Inverted psoriasis L40.83
Psoriasis inversa: 85-year-old patients, Zn of severe exanthematic psoriasis years ago, all healed, but submammary severe psoriasis inversa again and again. stable healing under MTX 5 mg/week + tacrolimus topically 1 x daily
Contact dermatitis allergic L23.0
Psoriasis capitis L40.8
Psoriasis capitis. solitary, chronically stationary, sharply defined, silvery scaly plaque that extends beyond the hairline. infestation of predilection sites on the rest of the body
Superficial tinea capitis B35.0
Tinea capitis superficialis: multipe whitish scaly, moderately itchy papules and plaques. no pre-treatment.
Dermatomyositis (overview) M33.-
Dermatomyositis (V-sign): Characteristic cutaneous symptoms of the backs of hands and fingers, almost proving the diagnosis of "collagenosis", with reddish-livid papules arranged in stripes, which merge to form flat plaques in the area of the end phalanges. Painful nail fold keratoses with parungual erythema are sometimes seen. Such papules arranged on the stretching side are also found in SLE and mixed collagenosis, rarely once in lichen planus.