Image diagnoses for "red"
911 results with 4584 images

Pyoderma gangraenosum: progressive, painful ulcer that has been present for several months in patients with known MGUS

Pyoderma gangraenosum: deep, painful ulcer that has existed for several months; ulcerative colitis ulcerosa that is located at the base of the tract.

Purpura pigmentosa progressiva: etiologically unexplained (medication?) pronounced clinical picture that has been changing for several months with symmetrically distributed, disseminated, non-itching, yellow-brown, spots.

Purpura pigmentosa progressiva: aetiologically unexplained (medication?) pronounced clinical picture that has been changing for several months with symmetrically distributed, disseminated, non-itching, yellow-brown, spots (detailed picture).

Purpura pigmentosa progressiva. incident light microscopy, blurred, yellow-brownish spots (star), in addition to punctiform, fresh bleeding (horizontal arrow) also older brown-reddish spots already in decomposition (vertical arrow). line pattern: traced skin line pattern of the skin of the lower leg

Purpura pigmentosa progressiva. reflected light microscopy, blurred, yellowish-brownish spots (haemosiderin) next to punctiform, fresh bleedings.

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.

Purpura thrombocytopenic: line shaped, fresh skin bleeding (diascopically not pushable away) after intensive scratching.

Purpura thrombocytopenic: line shaped, fresh skin bleeding (diascopically not pushable away) after intensive scratching

Purpura, thrombocytopenic: colorful picture with fresh, punctiform, red bleedings as well as older, yellowish, hemosiderotic inclusions (see following figure)

Purpura, thrombocytopenic (detailed illustration): fresh haemorrhages are marked by arrows; yellowish haemosiderin deposits are circled and marked by stars.

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.

Cellulitis, eosinophilic. early phase: Clear pruritus and dolent burning for several days. The differently sized erythema and rich red smooth plaques shown here have existed for 2 days.

Churg-Strauss Syndrome. circumscribed, borderline red, in the centre brown-yellow (here beginning of infiltrate formation and regression), in the area of the red areas rough, moderately pressure tolerated plaques and nodules in a 40-year-old man. known allergic bronchial asthma and seasonal rhinitis allergica. rennet: eosinophilia 45%; IgE >1000U/ml

Churg-Strauss syndrome: encircled central granulomatous regression zone (see histological preparation 1); on the right side the progression zone is outlined (see histological preparation 2).

Acute urticaria: acutely occurring, itchy exanthema with circulatory, also anular wheals.

Acute urticaria: Acute exanthema with multiple red wheals localized on the trunk and extremities, disseminated, flatly elevated, severely itching.

Acute urticaria. detailed view

Angioedema of the eyelids: acute, not itchy swelling of the eyelids of both eyes, cause remained unclear.

Acute spontaneous urticaria with angioedema; since a few days rather discreetly developed urticaria with recurrent angioedema of the eyelids (which characterizes the clinical picture).

Rosacea papulopustulosa: disseminated, intermittent papules and pustules that persist for weeks on reddened skin (questionable pretreatment with a glucocorticoid externum); variable feeling of tension of the facial skin.

Rosacea papulo-pustulosa: recurrent centrofacial pustular lesions

Rosacea papulopustulosa: detailed view of the changes in the forehead.

rosacea papulopustulosa: centrofacially localized redness, inflammatory papules and pustules. infestation of the eyelids. recurrent keratoconjunctivitis.

Rosacea papulopustulosa: grouped, inflammatory reddened papules and pustules that persist for weeks in phases; variable feeling of tension in the facial skin.