Image diagnoses for "Arm/Hand"
351 results with 786 images

Varicella: Detail of a vesicular exanthema existing since a few days; here shown a centrally navelled, already in regression, flat, hardly tensed pustule with an erythematous border.

Lipomas: spherical soft painless tumours that have reached this size over a period of 3-4 years, now without any growth tendency.

Dry keratotic plaque type Chronically active, intermittent plaques, which have existed for more than 20 years, especially on the palm of the hand, multiple, rough, partly reddish, scaly, blurred spots, plaques and rhagades in a 54-year-old man.

Scleroderma, circumscribed. untreated, ligamentous, circumscribed scleroderma with extreme atrophy of the skin, subcutaneous fatty tissue and muscles, joint contractures

Lichen planus anularis:few, ring-shaped, marginally progressive, centrally healing under hyperpigmentation, moderately itchy, lichenoid plaques; the lichenoid character of this lesion is recognizable in the marginal area by its livid colour and its surface gloss

Scabies. Severe mite infestation with overlying pyoderma.

Porokeratosis linearis unilateralis; first occurred 5 months ago; since then persistent, non-pruritic, brownish, sharply defined, circinous or garland-shaped, pityriasiform scaling papules and plaques on the trunk and right shoulder in a 60-year-old man.

Amyloidosis systemic: Flat light brown, symptomless plaques on both backs of the hands and fingers; recurrent fresh haemorrhages after banal traumas.

Lymphangitis acuta.

Pronounced, large-area allergic contact dermatitis: large, blurred (scattered edges), itchy, red, rough, slightly scaly plaques that have existedfor 4 weeks.

Mycosis fungoides (plaque stage): 72-year-old male (suction plaque stage of Mycosis fungoides); multiple, disseminated, 2.0-10.0 cm large, occasionally slightly itchy, only slightly increased in consistency, slightly scaly red, poikilodermatous plaques; conspicuous atrophy of the lesional skin (characteristics of the " Granulomatous slackskin")

Teleangiectasia syndrome, naevoides; for about 20 years existing, blurred redness of finest telangiectasia on the forearm of a 66-year-old woman.

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.

Toxic epidermal necrolysis. mostly picture of erythema exsudativum multiforme. necrolytic detachment of the skin beginning at the knee and lower leg.