Image diagnoses for "Macule"
332 results with 1231 images
Results forMacule

Nevus anaemicus Q82.5
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) Q82.3

Pityriasis versicolor alba B36.0
Pityriasis versicolor alba: spatter-like and fine spotted depigmentations with fine surface scales.

Ulerythema ophryogenes L66.4
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 (overview) B36.0
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 (overview) L80

Klippel-trénaunay syndrome Q87.2
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.

Chronic actinic dermatitis (overview) L57.1
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 (overview) M30.8
Livedo racemosa:generalized livedo racemosa with characteristic bizarre reddening of the skin, which typically does not form closed ring structures; no other organ alterations

Asteatotic dermatitis L30.8
Desiccation dermatitis: predominantly coarse lamellar desquamation of the altogether dry skin in the area of the abdomen, caused by treatment with isotretinoin.

Maculopapular cutaneous mastocytosis Q82.2
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 L93.0
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 I78.8
Teleangiectasia. Harm sleeve, reticularly branched, irregular vascular dilatations in the area of both cheeks.

Mastocytosis (overview) Q82.2
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 E80.1
Porphyria cutanea tarda: dirty brown hyperpigmentation; hypertrichosis in the area of the temple and cheek.

Acrocyanosis I73.81; R23.0;
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 E27.1
Addison's disease: generalized hyperpigmentation with spotty, grayish-brownish pigment deposits in the lower lip red in a 22-year-old man.

Ulerythema ophryogenes L66.4
Ulerythema ophryogenes in pronounced "keratosis pilaris syndrome"; conspicuous symmetrical redness of both cheeks.

Lupus erythematosus acute-cutaneous L93.1
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.

Purpura pigmentosa progressive L81.7
Purpura pigmentosa progressica (type: Purpura anularis teleangiectodes): brown-red anular, also cocard-like (ring-in-ring structure) by confluence also serpiginous foci. no significant itching. sporadically also largely faded only shadowy spots.

Juvenile dermatomyositis M33.0

Hand-foot-mouth disease B08.4
Hand-Foot-Mouth Disease: since about 1 week, painful, blisters, pustules and papules on hands and feet; about 2 weeks before, unspecific flu-like prodromas.

Meese cross bands L60.8
Meese transverse ligaments: Pre-existing Sézary syndrome. Distinct whitish transverse ligaments of the nails, of which proximally situated discrete leukonychia.

Hyperpigmentation caloric L81.8
Hyperpigmentation caloric. for several years irregular heat applications due to back problems.
