Image diagnoses for "Torso", "Macule"
156 results with 395 images

Pityriasis rosea: Characteristic exanthema that exists for a few weeks, only slightly itchy, and orientation in the cleavage lines is visible.

Type I Neurofibromatosis, peripheral type or classic cutaneous form. Since puberty slowly increasing formation of these soft, skin-coloured or slightly brownish, painless papules and nodules. Several café-au-lait spots.

Chronic photo-ageing of the skin: moderately pronounced photo-ageing of the skin; in addition to an extensive base tan, irregularly configured pigment spots; further splashes of depigmentation.

Drug exanthema maculo-papular: almost erythrodermic, since a few days existing, strongly itching (and painful; skin is sensitive to touch) maculo-papular exanthema, preceded by a feverish viral infection which was treated with antibiotics and non-steroidal anti-inflammatory drugs.

Circumscribed scleroderma (type Atrophodermia idiopathica et progressiva ): since about 2-3 years first appearing, since then size progressive, large brown, little indurated, non-symptomatic spots in the area of the trunk in a 23-year-old female patient.

Dermatomyositis. red-violet, occasionally itchy, flat erythema in the décolleté and on the sides of the neck. general fatigue and muscle weakness.

Urticaria pigmentosa: General view: about 0.5-1.0 cm large, disseminated, roundish, brownish-red spots. Only when rubbed, the spots redden more strongly with accompanying itching. Increased reddening and itching even in warm showers or baths.

Atrophodermia idiopathica et progressiva: Large, red, confluent, barely palpable, smooth, sharply defined, symptom-free patches/plaques that slowly expand over months.

Neurofibromatosis peripheral: Café au lait spots in neurofibromatosis type I.

Exanthema subitum. 2-year-old boy with a severe disturbance of the AZ and an acute high fever of 40 °C. Macular exanthema with densely packed red-brown spots of different size and no symptoms.

Naevus flammeus: congenital, completely symptomless vascular malformation (exclusively capillary malformation) without tendency to tissue hypertrophy.

Nevus, melanocytic. Congenital melanocytic nevus of the spilus nevus type

Systemic lupus erythematosus:chronic, locally constant exanthema consisting of spots, papules and plaques; concomitant: recurrent fever attacks, fatigue and tiredness, arthralgia, inflammation parameters +, ANA high titer positive, rheumatoid factor +, DNA-Ak+.

Complicative folliculitis with initial erysipelas and lymphangitits.

Varicella: generalized exanthema with coexistence of vesicles, papules and incrustations.

Bullous Dermatitis solaris. multiple, acute, generalized, 24-hour-old, 0.3-3.0 cm large, isolated and grouped, red, bulging blisters (II degree burns) occurring in UV-exposed areas, localized on a large, homogeneous, painful erythema.

Erythema dyschromicum perstans. clinical picture existing for months. initially small spots of brown-red with little increase in consistency, later large, steel to slate grey, smooth spots and plaques of the skin. no medication history.