Image diagnoses for "Macule", "red"
197 results with 635 images

Purpura thrombocytopenic: Hemorrhagic spots with a tendency to confluence, existing on both lower legs with emphasis on the extensor sides. It is a drug-induced form of a thrombotic- thrombocytopenic purpura with hemolytic microangiopathic anemia and central nervous failure symptoms. The trigger was the ingestion of non-steroidal anti-inflammatory drugs. Sudden onset with fever, disorientation, stupor.

Erythronychia, localized longitudinal detail magnified by reflected light microscopy; solitary, painless, red longitudinal striation of the nail plate with slight, V-shaped retraction and several splinter hemorrhages.

mononuleosis, infectious. generalized (almost universal) macular exanthema. raspberry tongue with swollen papillae. tongue surface completely free of coating.

Vasculitis leukocytoclastic (non-IgA-associated): multiple, for about 10 days existing, localized on both lower legs, irregularly distributed, 0.1-0.2 cm large, confluent in places, symptomless, red, smooth spots (not compressible).

Eczema atopic (erythrodermal): severe, universal (erythrodermal) atopic eczema, exacerbation phase for about 3 months.

Spider veins. Multiple, radially spread, radiating vascular dilatations of different calibre, partly in the skin level, without symptoms, persisting for several years, as if drawn with a thin pencil, located at the level of the skin, on the integument of a 77-year-old female patient. In the centre confluence of the filigree vascular strands to a bluish red spot.

Purpura Schönlein-Henoch. seeding of smallest petechiae beside fresh and older haemorrhagic maculae.

Tinea inguinalis: plaques that have existed for several months, coarse lamellar scaling and moderately itchy. Mycological evidence of T. rubrum.

Vasculitis, leukocytoclastic (non-IgA-associated). multiple, acute, symmetric, since 2 weeks existing, localized on both lower legs, irregularly distributed, 0.1-0.2 cm large, sharply defined, symptomless, hemorrhagic spots and blisters as well as beginning incrustations.

Dermatitis chronic actinic. detail enlargement: Disseminated, scratched papules and nodules as well as blurred, large-area, red, sharply itching fine-lamellar scaling spots and plaques in the face of a 51-year-old female patient with atopic eczema existing since birth.

Epidermolysis bullosa simpex, Weber-Cockayne: after banal traumas visible blistering or only simple detachment of the epidermis. scarless healing.

Klippel-Trénaunay syndrome: extensive vascular malformation with extensive nevus flammeus affecting the trunk, the right arm and both legs. No evidence of soft tissue hypertrophy so far. No AV fistulas.

Livedo racemosa generalisata: extensive, bizarre, haemorrhagic reticulation of the skin

Chilblain lupus: reflected light microscopy. dilated, corkscrew-like vessels (arrows) on the dorsal side of the fignerendl song. s. clinical picture. encircles the anemic pressure point of the reflected light microscope

Livedo racemosa: Detail view of the bizarre erythema figures.

Dermatomyositis: Beginning poicilodermic condition of the skin with hypopigmentation, telangiectasia and epidermal atrophy in a 33-year-old woman.

Dermatitis solaris: painful, extensive and painful erythema and blistering, clearly marked on areas exposed to sunlight, following several hours of exposure to the sun.

dermatomyositis. red-violet, slightly itchy, flat. blurred erythema in the décolleté and on the lateral parts of the neck. general fatigue and muscle weakness.