Image diagnoses for "Macule"
331 results with 1225 images

Lupus erythematodes tumidus: Plaques existing for 3 months, localized on the back and face, irregularly distributed, sharply defined, 0.2-3.0 cm in size, flatly raised, clearly increased in consistency, slightly sensitive, red, smooth plaques; no significant scaling.

Amyloidosis systemic of the Al type. after banal efforts or local trauma completely symptomless, permanently persistent purpura. on intensive examination a flat, symptomless discoloration (amyloid deposits) of the anterior neck area is noticeable. known plasmocytoma.

Erythrodermia. universal, chronically stationary, for 3 months constant reddening of the skin with leather-like infiltrated, diffusely pigmented, brown-red (melanoerythrodermia), occasionally also diffusely weeping skin. palmoplantar hyperkeratosis; onychodystrophy; diffuse alopecia; pruritus. generalized lymphadenopathy. erythrodermia in cutaneous T-cell lymphoma.

Differential diagnosis "Naevus anaemicus"; naevus depigmentosus; congenital white spot, calm, not cracked boundary pattern, after vigorous rubbing the lesional skin reacts with nromal reactive redness.

Urticaria pigmentosa: approx. 0.5-1.0 cm in size, disseminated, roundish, brownish-red spots. Only when rubbed, the spots become more red with accompanying itching. Increased redness and itching even in warm showers or baths.

erythema infectiosum. after slight "flu-like" infection intensive redness (and swelling) of both cheeks (cheek whistle face). 2 days later little symptomatic exanthema with anular erythema on the arms. cervical lymphadenopathy. laboratory: o.B.

Teleangidectasia: irregular caliber, in places ectatic capillaries in a nodular basal cell carcinoma.

Exanthema subitum. exanthema with centrifugal spread from the trunk to the neck and back of the head. recess of the face.

generalized cGVHD: generalized, scleroderma-like, hardly itchy generalized skin disease. graft-versus-host disease occurred about 2 years after stem cell transplantation. poikiloderma with bunchy, hyper- and depigmented indurated plaques.

Café-au-lait spots: in neurofibromatosis type I. Several medium brown spots in the lumbar region.

Chronic actinic skin damage: pronounced chronic light damage to the skin with poikilodermatic skin; years of excessive, chronic sun exposure.

Self-tanner: uneven browning of the cheek area after application of a self-tanning external layer.

Lentigo maligna with transition to a lentigo maligna melanoma: 68-year-old man, presenting in practice because of eczema. On questioning the completely symptomless "spot" on the earlobe has slowly grown over the years. Excision with histology: Both parts of a lentigo maligna and (central) parts of a lentigo maligna melanoma, TD 0.4mm, pT1a.

Erysipelas. edema of both lower legs and back of the foot with redness and overheating, here in connection with a tinea pedum. absence of fever and general symptoms; the ASL titre is elevated.

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

Mycosis fungoides follikulotrope: 10-year-old girl with generalized folliculotropic Mycosis fungoides. foudroyant course of the disease which made a stem cell transplantation necessary

Vitiligo: extensive white areas with residual stripey pigmentation in the area of the shoulders, neck and décolleté.

Mycosis fungoides, folliculotropic. 3-year-old clinical picture with strongly itchy, moderately sharply defined, follicular red plaques.

Dermatitis perioralis. solitary, chronically active, centrofacially localised (white perioral border), large, inhomogeneous, blurred, itchy and constantly burning, red, rough spot (erythema). additionally numerous, follicular papules and individual pustules.