Image diagnoses for "red", "Leg/Foot"
279 results with 764 images

drug reaction, lymphocytes: multiple, non-symptomatic, surface-smooth papules and plaques. occurred several months after cardiological readjustment. patient otherwise healthy. no evidence of lymphatic systemic disease. no other drugs. histological: nodular, mature lymphocytic tissue. no lymph follicles.

Erythema chronicum migrans. large plaque, which has been growing steadily on the periphery for about 8 months, only slightly increased in consistency, homogeneously brownish in the centre, somewhat atrophic, marked by an increasingly consistent erythema zone at the edges. only occasionally "slight pricking" in the lesional skin.

Necrobiosis lipoidica: a condition that has existed for years and is constantly worsening; no diabetes mellitus known.

Lichen planus. chronically active, multiple, increasing, disseminated standing, partly confluent, first appearing about 6 months ago, mainly localized at the inner edge and back of the foot, 0.3-0.6 cm large, itchy, red, smooth, shiny papules in a 46-year-old woman. similar papules appeared on both inner wrist sides. Furthermore, a whitish, net-like pattern of the buccal mucosa of the mouth appeared.

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

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

Bowen's disease with transition to Bowen's carcinoma: solitary, size-progressive plaque that has been present for several years, occasionally accompanied by itching, sharply and arc-shaped, border-emphasized plaque with increasing verrucous nodular formation (see following figure).

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.

Syphilis acquisita: papular, completely asymptomatic (recurrent) exanthema (no itching) Important: generalized lymphadenopathy.

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.

Cholesterol embolism: extensive, progressive, flat ulcerations with necrotic deposits, highly painful margins and livid erythema in a patient with AVK.

Livedovasculopathy: haemorrhagic-necroticlesions on erythematous ground. periulcerous livedo image. healing leaving star-shaped, whitish scars.

Dermatosis, IgA-lineare. for several years intermittent clinical picture with multiple, considerably itchy, 1.0-2.0 cm large, roundish or stripe-shaped erythema, papules, papulo vesicles and encrusted erosions.

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).

Dermatofibroma, hemosiderin storing tumor on the lower leg of a 64-year-old female patient.

Dimorphic leprosy of the lepromatous type: borderline leprosy of the lepromatous type with multiple, large, plate-like, borderline inflammatory lesions (type I leprosy reaction).