Image diagnoses for "Macule"
321 results with 1208 images

Urticaria pigmentosa:differently sized, disseminated, flat, oval or round, brownish-red spots on the trunk, buttocks and thighs; 52-year-old female patient. Continuous proliferation of the spots for years. No evidence of systemic infestation.

Lentigo maligna melanoma: Plaque with nodular parts, known for years, first brown, then gradually black, asymmetric, multicoloured, bizarrely limited plaque with nodular parts; the histological diagnosis was made from the nodular part.

Nappes claires. Numerous bizarre bright recesses in erythroderma.

Ecchymosis syndrome, painful. intermittent manifestation of painful skin bleeding in a 52-year-old manic-depressive woman. Initial development of edematous, overheated, pressure-sensitive erythema, followed by development of bleeding and slow expansion of the skin changes.

Pityriasis versicolor alba: irregularly distributed, symptomless, bright spots that appeared after repeated exposure to sunlight.

Lentigo-maligna melanoma: a slow-growing, initially homogeneously brown, then multicoloured, black "spot", which has been known for several years and can now be felt in places as a sublimity.

Lupus erythematosus, subacute-cutaneous. detail magnification: Multiple, solitary or confluent, small spots to large areas, sharply defined, anular and gyrated erythema of neck and face of a 68-year-old female patient, partly covered with yellowish crusts.

Lentigo solaris. solitary, chronically stationary, 0.8 x 0.6 cm large, sharply defined, inhomogeneously coloured, symptomless, brown, smooth spot. 74-year-old female patient with strong UV exposure.

Spider veins. dark blue-red, 0.5-2.0 mm wide, tortuous varicose veins with irregular, ampulla- or nodular ectasia on the medial right thigh of a 69-year-old woman.

Dermatomyositis. acutely occurring heliotropic, succulent purple exanthema; typical, pronounced, sharply marked, periorbital and perioral paleness. general fatigue, muscle weakness.

Multiple telangiectasias in Urticaria pigmentosa adultorum.

Klippel-Trénaunay syndrome with syndactyly , CVI and lymphedema.

acrodermatitis chronica atrophicans: 69-year-old woman. for 4 months right lower leg flat livid-red. at the beginning somewhat edematous. not overheated. subjectively symptomless except for slight hyperesthesia lateral foot edge on the right. no improvement by elevation. no tick bite recallable. in the laboratory confirmation of Lyme disease (high titer IgG, low titer IgM). no further manifestations except ACA.

Klippel-Trénaunay syndrome: extensive, bilateral vascular malformation of capillary (naevus flammeus) and venous vessels (varicosis with chronic venous insufficiency - CVI); distinct soft tissue hypertrophy on the left side; no pelvic obliquity!

Phlebektasia. Suction. lip margin angioma. Harmless, bluish, soft and expressive lump of the lower lip.

Differential diagnosis of discoloration of the nail: Melanocytic neoplasms of the nail matrix always lead to longitudinal striation of the nail plate.

Ephelids: in summer occurring, symmetrically localized bizarre pigment spots barely 0.2cm in size, light to dark brown.

Multiple telangiectasias in progressive systemic scleroderma.