Image diagnoses for "Arm/Hand"
352 results with
787 images
Results for Arm/Hand
Lichen planus (overview) L43.-
Lichen planus classic type: for several weeks persistent, red, itchy, polygonal, partially confluent, smooth, shiny papules.
Lipoma (overview) D17.0
Lipoma: A subcutaneous lump on the upper arm which has existed for years, is completely unattractive and asymptomatic, can be easily delimited and slides over the underlying tissue.
Nevus anaemicus Q82.5
Differential diagnosis "Naevus anaemicus"; naevus depigmentosus; congenital white spot, calm, not cracked boundary pattern, after vigorous rubbing the lesional skin reacts with nromal reactive redness.
Atopic dermatitis in infancy L20.8
Atopic dermatitis in infancy, therapy resistant eczema foci on both hands.
Atopic dermatitis (overview) L20.-
Eczema, atopic. chronic, red, blurred, large, severely itchy, rough plaques on lichenified skin. the elbows and face are also affected.
Atopic dermatitis in children and adolescents L20.8
Childhood eczema atopic: skin lesions in a 12-year-old boy. Back of the hand gray, dry, lichenified. No dermatitis. No itching.
Papulosa juvenilis dermatitis L30.8
Dermatitis papulosa juvenilis: flat, 0.1-0.3 cm large, hemispherical or roundish, also polygonal, low inflammatory lichenoid papules.
Erythema multiforme, minus-type L51.0
erythema multiforme: detailed picture: suddenly appeared, for 4 days existing, itchy, disseminated exanthema with cocard-like plaques. the skin changes appeared shortly after the beginning of antibiotic therapy for urinary tract infection. here the finding on the back of the hand. s. isomorphism (koebner phenomenon).
Erythema multiforme, minus-type L51.0
erythema exsudativum multiforme. suddenly appeared, since 4 days existing, itchy, disseminated exanthema with cocard-like plaques. the skin changes appeared shortly after the beginning of antibiotic therapy for urinary tract infection. here the finding on the back of the hand. s. isomorphism (koebner phenomenon).
Erythema multiforme, minus-type L51.0
erythema exsudativum multiforme. typical picture with different stages of development of the efflorescences. besides fresh smaller, flat papules, further developed, older larger plaques with discrete cocard structure. some plaques with indicated central vesicles.
Cutaneous mastocytoma Q82.2
Mastocytoma kutanes: 1.0 x 2.0 cm, yellow-brown, flat, crescent-shaped, raised lump with blurred edges, protruding in the first two months of life; normal surface relief above the lump.
Cutaneous mastocytoma Q82.2
Multiple mastocytoma: disseminated, flat brownish reddish, itchy, smooth patches and plaques on the right foot or lower leg of a 4-month-old boy; the intact surface pattern of the field skin over the lesioned skin is shown in the inlet.
Cutaneous mastocytoma Q82.2
Multiple mastocytomas: disseminated, flat, brownish-reddish, itchy, smooth patches and plaques on the trunk and extremities of an 8-month-old boy; attention should be paid to the intact surface pattern of the field skin over the lesional skin.
Milia L72.8
Milia. reflected light microscopy: milia in the cheek area. whitish, pearly round foci (marked with arrows), surrounded by a light red border and numerous vellus hair follicles.
Tinea corporis B35.4
Tinea corporis:Acute, solitary, ring-shaped, approx. 2.5 cm large, sharply defined, itchy plaque, which has existed on the right wrist for several weeks, is increased in consistency at the edge and has fine lamellar scales, and has healed centrally in a 12-year-old girl (pathogen: Mikrosporum canis).
Scleroderma systemic M34.0
scleroderma systemic: oedematous swelling of the hands and fingers. when stretching the fingers, white discoloration of the tense skin areas occurs. raynaud's syndrome, known for several years. reduced performance, increased sensitivity to cold, rheumatoid joint complaints, ANA:1:320; SCL70AK+.
Disabling pansclerotic Morphea L94.1
Scleroderma, circumscribed. untreated, ligamentous, circumscribed scleroderma with extreme atrophy of the skin, subcutaneous fatty tissue and muscles, joint contractures
Disabling pansclerotic Morphea L94.1
Scleroderma, circumscribed. Pan-sclerotic, mutant form in a 15-year-old boy.
Atrophodermia idiopathica et progressiva L90.3
Atrophodermia idiopathica et progressiva. chronic stationary, map-like spread, brownish spots. the existing skin changes have developed within 2-3 years.
Circumscribed scleroderma L94.0
Band-shaped circumscribed scleroderma: brownish plaques that have existed for years and are progressive, symptom-free.
Vitiligo (overview) L80
Vitiligo: on the upper part of the upper arm spatter-like vitiligo, on the forearm extensive depigmentation.