Image diagnoses for "skin-colored"
277 results with 598 images

Cheilitis actinica chronica: Scaly flat leukoplakia with rhagade formation.

Cheilitis actinica chronica: extensive veil-like leukoplakia of the red of the lips with increased radial furrowing.

Cheilitis actinica chronica: extensive, non-inflammatory, leukoplakische change of the lip red. at the lower lip blurred transition to the lip skin.

Alopecia androgenetica in men. stage IV: confluence of anterior and posterior hair thinning in the parietal region.

Graft-versus-Host Disease, chronic: 1.5 years after stem cell transplantation, large-area scleroderma with significant movement restriction, significant reduction of the AZ

Granuloma anulare, plaque type: multiple, completely symptomless, faded in the center, smooth, painless anular plaques.

Apocrine cyst of the sweat gland at the medial edge of the lower eyelid (marked by arrow).

Eyelid swelling: massive swelling of the eyelids in the case of known contact allergies to various cosmetics.

Ulerythema ophroygenes (here atrophic terminal stage): Complete loss of the lateral parts of the eyebrows; no more follicular ostia visible.

Keratoses seborrhoeic: multiple skin-colored flat wart-like papules and plaques. occasional itching.

Swelling of the eyelid: Recurrent, painless swelling of the left upper lid (always) in Melkersson's disease - Rosenthal's syndrome

Atrophy, senile: age-related involution of the lip skin with radial furrow formation.

Lipomas: spherical soft painless tumours, no longer growing.

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.

Madelung-Fatthals: for years increasing fatness of the neck region.

Dermal melanocytic nevus: melanocyticnevus known since earliest childhood, initially dark brown, slightly raised, skin-coloured in the past decades. completely unchanged for several years. 0.9 x 0.9 cm diameter, moderately firm, sharply defined, calotte-shaped skin-coloured papules. 78-year-old patient.

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

Scleroderma circumscribed pansclerotic: 12-year-old boy of oriental origin. 3 months ago first appeared, strongly progressive sclerosis, partly ulcerated and covered with blackish necroses. A highly febrile disease of unexplained aetiology lasting more than 3 days preceded the skin symptoms by 14 days.

Hemiatrophia faciei progressiva (Perry Romberg) patient 3 years later.

Hemiatrophia faciei progressiva: Progress documentation, Figure 2: 12-year-old female patient with clear perceptible changes in the disease.

Hemiatrophia faciei progressiva: Progress documentation, Figure 3: Neurological (facial paresis) and ophthalmological (oculomotor paresis) complications in the context of circumscribed scleroderma en coup de sabre at the age of 16

Atrophy of the skin surface with wrinkled surface appearance.

Scabies (in the infant). strongly itching blisters and blisters in the area of the sole of the foot in a toddler. infants tend to have an "excessive" blistery inflammatory reaction to the mite infection when infected for the first time.

Ulerythema ophryogenes: bilateral ulerythema with discreet reddening of the skin and redness of the lateral eyebrows