Image diagnoses for "Skin depressions", "skin-colored"
33 results with 72 images

Artifacts. Completely unsystematic, striated scarring.

Necrobiosis lipoidica: Necrobiosis lipoidica that has existed for several years. Large, atrophic scarring (translucent vessels) in the centre. Reddened progression zone at the edges.

acne conglobata. multiple comedones in the area of nose, cheeks and neck of a 53-year-old patient. irregular skin surface with pronounced scarring, predominantly deeply indented. approx. 2 cm large hyperpigmentation at the root of the nose.

Aplasia cutis congenita. general view: 1.5 x 1.2 cm in size, hairless, slightly sunken, yellowish-whitish area with shiny surface, existing since birth, unchanged for years except for size increase during physical growth.

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

Involution of the subcutaneous fatty tissue of the thighs with transverse, bulging wrinkles.

Scléroderma en coup de sabre: for a few months, conspicuous, broad band-shaped reddened plaque.

Striae cutis distensae. older, whitish, differently long and wide, jagged, parallel or diverging atrophic stripes with slightly sunken and thinned skin.

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

Acne conglobata: symmetrically distributed, eminently chronic, inflammatory and melting papules and pustules as well as strong, retracted scar formation, with retention fluctuating in places.

Circumscript scleroderma (profound type): pronounced atrophy of cutis, subcutis and fascial tissue. resistance to therapy.

Kindler Syndrome: Atrophy ofthe skin with reticular pigmentation and circumscribed erythema

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

Acne conglobata. Scarred healed acne conglobata.

Leprosy lepromatosa: stiffening of the fingers in a claw-like position. closure of the fist no longer possible. atrophy of the interosseous musculature (see following figure).

Kindler syndrome: blistering since birth; now poikilodermatous appearance.

Atrophy of the skin surface with wrinkled surface appearance.

Cutis rhomboidalis nuchae, fieldedfolds of skin in massive elastosis actinica in a 75-year-old patient; the clinical picture is pathognomonic.

Lichen sclerosus extragenitaler: Progressive lichen sclerosus for 2 years with a clearly sunken scarring of the lower lip and chin; surrounding, flat, blurred, clearly consistent plaque with a red-white coloration in the chin area (here the clinical features of the lichen sclerosus are visible).

Pronounced livedo racemosa: Intermediate findings after 2 more years (period of clinical follow-up over a period of 8 years); extensive scar healing after therapy with high-dose venous immunoglobulin therapy (IVIG)

Atrophy of the skin: age-related flabby atrophy of the dorsal skin with partly swirled, partly parallel, vertical wrinkles; no significant light aging