Image diagnoses for "Macule", "red"
187 results with 616 images

Malformations, syndromal vascular: Nevus flammeus (capillary malformation, no arterio-venous anastomoses) with soft tissue atrophy and pelvic obliquity, no pain symptoms.

Hematoma, nail hematoma. reflected light microscopy with blue, sharply defined discoloration of the nail.

Vasculitis, leukocytoclastic (non-IgA-associated). exanthematic seeding of dense macular to maculopapular reddish-brownish efflorescences.

Vasculitis, leukocytoclastic (non-IgA-associated). multiple, acute, symmetric, localized on both lower legs for 1 week, irregularly distributed, 0.1-0.2 cm large, sharply defined, symptomless, red, smooth patches (non-compressible). Occurrence after flu-like infection and ingestion of a non-steroidal anti-inflammatory.

Teleangiectasia macularis eruptiva perstans. 58-year-old patient with a generalized, spot-like clinical picture which has existed for years and shows a constant progression. Itching during sweat-inducing efforts and mechanical exposure of the affected skin areas. Bizarre teleangiectatic vascular convolutions are characteristic.

Erysipelas, recurrent with pronounced lymphedema (see protruding follicle structure).

Livedo racemosa: bizarre pattern with sharply interrupted, age-interpreted ring structures

Benzyl nicotinate: toxic reaction after application of the cosmetic "Lip Injection" on the forearm; erythema extending beyond the application site with lymphangitic reaction 10 min. after application of the product.

Phospholipid-antibody syndrome. In the area of the lower leg and the ankle region of a 35-year-old woman localized, older, streaky, whitish scar areas which are surrounded by a yellowish-brownish coloration (postinflammatory hyperpigmentation). In the transition area to the sole of the foot a reticular, reddish-brown vascular drawing (Livedo racemosa) is impressive on the inside. Secondary findings are arterial hypertension. Several miscarriages are known from history.

acute erysipelas. acutely appeared, since a few days existing, increasing, flat, sharply defined, pillow-like raised, flaming red swelling of the left cheek and eye. vesicles and blisters. distinct impairment of the general condition with fever.

Erythrosis interfollicularis colli. chronic light damage without any subjective symptoms.

Vasculitis, leukocytoclastic (non-IgA-associated). multiple, since 1 week existing, on both lower legs localized, irregularly distributed, 0.1-0.2 cm large, confluent in places, symptomless, red, smooth spots (not compressible).

Dermatitis chronic actinic: An almost sharply defined flat eczema reaction on the back of the hand that has persisted for months and occurred after short gardening.

Chilblain lupus. early stage with livid-red, smooth, painful plaques. clinical picture reminiscent of chilblain (frostbite lupus). acrocyanosis still moderately pronounced.

Eczema atopic (overview): severe, universal (erythrodermic) atopic eczema. exacerbation phase since about 3 months. patient with rhinitis and conjunctivitis with pollinosis. total IgE >1.000IU.

Arthritis, psoriatic. solitary or multiple, chronically dynamic, recurrent, salty arthritis, especially of the small finger joints with erythematous, severe swelling and pain (sausage fingers). joint infestation ?in the beam?. usually also typical psoriatic lesions at the predilection sites.

Scleroderma, systemic: within a few years, newly developed telangiectasia of the facial skin in previously known systemic scleroderma.

Mononucleosis, infectious. generalized, non-itching exanthema in a 17-year-old woman. painful lymphadenopathy (neck, nape of neck). little itching, urticarial, small spotted, confluent exanthema in places with distinct emphasis on face and trunk.

Stria cutis distensae in exogenous Cushing's syndrome.