Image diagnoses for "red"
877 results with 4458 images

Contagious impetigo, large-bubble (bullous impetigo)

Naevus flammeus (Port-wine stain): fuzzy-limited red vascular nevus on the forehead (spreading area of N.V1 and NV2) and cheeks.

Chronic (atopic) cheilitis with perioral eczema: apart from dry skin and a known pollen sensitization (early bloomer) no other signs of atopic eczema. Known atopic diseases in the family.

Lichen planus exanthematicus: Itchy exanthema with 0.1-0.2 cm large, slightly raised, partly isolated, but also aggregated to larger plaques, smooth, shiny, red (also erosive) papules.

Bullosis diabeticorum: Spontaneously occurring extensive subepithelial blister formation on both lower legs after a banal extensive trauma. Slight burning sensation. No fever. No lymphadenitis. Pemphgoid AK negative.

Malformations of the vascular fronto-temporal nevus flammeus (Sturge-Weber-Krabbe syndrome)

Acute urticaria: acutely occurring, itchy exanthema with roundish, also anular wheals; distinct halo formation.

Pemphigus chronicus benignus familiaris: chronic, extremely therapy-resistant, sharply defined, rough, red,border-emphasized plaques in the area of the armpit; in the surrounding area, some already healed areas.

Ulcerated squamous cell carcinoma: cauliflower-like, firm, less pain-sensitive, eroded and ulcerated, weeping nodule, which has been present for > 1 year and is constantly enlarging.

Granuloma anulare, classic type . borderline, in the centre skin-coloured, smooth, painless, firm papules and plaques with the formation of an indicated ring shape without scaling over the middle joint of the left middle finger.

Systemic lupus erythematosus: Detailed view of the protruding follicular structure in the area of the lesional plaques.

Ulcus cruris venosum, localised at a typical site (ankle region), large, moderately painful ulcer covered with fresh granulation tissue.

lymphoma, cutaneous t-cell lymphoma. type mycosis fungoides, tumor stage. painless, scaly, partly crusty plaque existing for years with slow knot formation and increasing growth rate. moderately firm consistency. extensive crust formation.

Stevens-Johnson syndrome: Acutely occurring vesicular exanthema with characteristic, bull's-eye erythema, plaques and blisters as well as extensive, painful erosions of red lips, lip mucosa, tongue and gingiva in an 18-year-old woman. Clear general feeling of illness.

eczema atopic in childhood: 14-year-old adolescent with generalized atopic eczema. striking grey-brown, dry skin. multiple scratched papules and plaques. extensive, therapy-resistant pyoderma on the left thigh (developed after traumatic abrasion)

Psoriasis palmaris et plantaris (plaque-type chronic inpatient plaquepsoriasis of the sole of the foot with coarse desquamation and painful hare formation. no topical pre-treatment

Vasculitis leukocytoclastic (non-IgA-associated): multiple, since 1 week existing, on both legs symmetrically localized, irregularly distributed, 0.1-0.2 cm large, confluent in places, symptomless, red, smooth spots (not compressible).

Psoriasis vulgaris. general view: multiple, solitary or confluent, nummular or large-area, erythrosquamous plaques on the buttocks of a 49-year-old woman with psoriasis vulgaris existing since adolescence. the skin lesions continue into the rima ani.