Image diagnoses for "Plaque (raised surface > 1cm)"
587 results with 2924 images

Dermatitis chronic actinic: An almost sharply defined flat eczema reaction on the back of the hand that has persisted for months and occurred after short gardening.

Tinea pedis oligosymptomatic type: no subjective sympotaxis. findings rather coincidental. circinar, grazing scaling. typical are raised scaling ruffs of the areas (marked by arrows). small plantar wart marked by circle, positive mycological evidence in the zone of the small toe marked by square.

Necrobiosis lipoidica: slightly indurated plaque and atrophic surface (parchment-like skin surface in the centre.

acanthosis nigricans benigna: known diabetes mellitus. velvety, sour transformation of the axillary skin. foetor by sweat decomposition.

Parapsoriasis en plaques, large: symptomless, well limited. disseminated stains and plaques. When the skin is wrinkled, a cigarette-paper-like pseudoatrophic architecture of the skin surface is visible (important diagnostic sign!).

Acanthosis nigricans (overview): benign acanthosis nigricans in a (obese) southern European. characteristic verrucous, blurred plaques. hyperhidrosis.

Larva migrans: after a tropical beach holiday several weeks ago, at times clearly itchy, in places still linear, but also flat, solid, scaly plaques; now healing after local therapy.

Porom ekkrines: red papule with scaly surface, existing since > 1 year, little symptomatic. 52 year old patient.

Systemic lupus erythematosus: pronounced findings with bilateral, symmetrical, flat plaque formation in the décolleté. Apparent UV-emphasis. Fine central scarring in the plaques.

Lichen sclerosus of the vulva: homogeneous whitish sclerosis of the vulva and the perineum; phenomenon of a gaping vagina; 6-year-old girl

Pemphigus chronicus benignus familiaris: Multiple, chronically dynamic (changing course), greasy, sharply defined, red, rough plaques.

Keratosis palmoplantaris cum degeneratione granulosa. 25-year-old man has a chronic, congenital, smooth, evenly distributed, waxy thickened and yellowish discoloured plaque formation of both palms of the hand. The same skin lesions are found on the soles of the feet. It is an autosomal dominant inherited palmoplantar cornification disorder.

Psoriasis: Extensive, untreated plaque psoriasis, in addition to larger, in places confluent plaques, smaller papules and plaques as a sign of shear activity.

Pustulosis palmaris et plantaris: marked by square: fresh and older pustules. The two upper pustules with collateral erythema. Marked by arrows: brown, flat papules, as remains of older dried pustules.

Systemic lupus erythematosus (late onset): chronic, blurred reddish-livid plaques with spatter-like whitish spots, small erosions and crusts; accompanying recurrent fever attacks, fatigue and tiredness, arthralgia, inflammation parameters +, ANA high titer positive, rheumatoid factor +, DNA-Ak+.

Psoriasis of the hands: here partial manifestation in the context of generalized psoriasis, the acral affection led to psoriatic onychodystrophies.

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.