Image diagnoses for "Macule"
321 results with 1208 images

Klippel-Trénaunay syndrome: extensive vascular malformation with extensive nevus flammeus affecting the trunk and both arms with distinct soft tissue hypertrophy of the right arm.

Systemic lupus erythematosus: acute maculopapular exanthema, accompanied by recurrent fever attacks, fatigue and tiredness, arthralgia, inflammation parameters +, ANA high titer positive, rheumatoid factor +, DNA-AK+.

naevus anaemicus in periperous neurofibromatosis. coin-sized to palm-sized, almost jagged, white spot (here marked by arrows). this bizarre spot is visible with varying degrees of clarity. it is particularly noticeable when the surrounding area is reddened as a "negative contrast". after intensive rubbing of the spot, no reddening is visible in the area of the spot. .

Incontinentia pigmenti, Bloch-Sulzberger type. Garland-shaped pigmentation on the mother's thigh.

Pityriasis versicolor alba: spatter-like and fine spotted depigmentations with fine surface scales.

Ulerythema ophryogenes: the area marked by the square shows follicular papules (keratosis follicularis) on an enlarged scale with a reddened courtyard which merges into a two-dimensional erythema.

Pityriasis versicolor: 50-year-old woman. for years always pityriasis versicolor upper back. this time presentation with flat and small spotted herds groin/mons pubis.

Vitiligo: Sharply defined, depigmented spots on the face of a 31-year-old patient with skin type IV.

Klippel-Trénaunay syndrome: Extensive vascular malformation with a large-area nevus flammeus affecting the trunk and the right lower extremity with soft tissue hypertrophy of the right lower extremity; pelvic obliquity.

Dermatitis chronic actinic (type light-provoked atopic eczema). general view: Disseminated, scratched papules and plaques, nodular in places, as well as blurred, large-area, reddened, severely itching erythema on the face of a 51-year-old female patient with atopic eczema existing since birth. the skin changes can be provoked by sunlight and photopatch testing.

Livedo racemosa:generalized livedo racemosa with characteristic bizarre reddening of the skin, which typically does not form closed ring structures; no other organ alterations

Desiccation dermatitis: predominantly coarse lamellar desquamation of the altogether dry skin in the area of the abdomen, caused by treatment with isotretinoin.

Urticaria pigmentosa. general view: Differently large, disseminated, flat, oval or round, exanthematically distributed, brownish-red spots on the trunk and thighs of a 34-year-old female patient. An elevated dermographism can be triggered.

Lupus erythematodes chronicus discoides. 5 years of persistent recurrent skin changes in a 25-year-old girl, despite disease-adapted therapy measures. Large flat, soft-red plaque (with still preserved follicles). Conspicuous (re-)pigmentation within a few weeks in the lesional skin (which was hypopigmented before).

Teleangiectasia. Harm sleeve, reticularly branched, irregular vascular dilatations in the area of both cheeks.

Mastocytosis. type: Multiple mastocytomas Multiple, chronically stationary, approx. 0.6 x 0.7 cm large, localized on the entire integument, disseminated, round to oval, brown, smooth, little itchy spots and plaques in a 4-year-old boy.

Porphyria cutanea tarda: dirty brown hyperpigmentation; hypertrichosis in the area of the temple and cheek.

acrocyanosis in right heart failure. extensive homogeneous reddening of the facial areas. clearly more prominent in cold weather. moderate cyanosis of the red of the lips. age involution of the chin region with oblique chin furrows. moist corners of the lips with occasional pearlèche.

Addison's disease: generalized hyperpigmentation with spotty, grayish-brownish pigment deposits in the lower lip red in a 22-year-old man.

Ulerythema ophryogenes in pronounced "keratosis pilaris syndrome"; conspicuous symmetrical redness of both cheeks.

Lupus erythematosus acute-cutaneous: a clinical picture known for several years with a variable course of the disease; extensive regression of the acute symptoms under immunosuppressive therapy.