Image diagnoses for "Plaque (raised surface > 1cm)"
559 results with 2838 images

Chronic contact allergic dermatitis: therapy-resistant, chronic dermatitis caused by beta-blocker-containing eye drops (in case of glaucoma). Only by changing the therapeutic agent a complete healing of the chronic dermatitis could be achieved. In the meantime a 1% hydrocortisone vaseline was applied twice a day.

Pemphigus chronicus benignus familiaris: chronic, extremely therapy-resistant, varying in size, sharply defined, rough, red, marginal plaques in the armpit area with marginal Collerette-like scaling

Dermatosis, acute febrile neutrophils (Sweet syndrome): acutely occurring (existing since 1 week) highfebrile exanthema with involvement of the trunk, face and capillitium as well as the upper extremities. feeling of illness, myalgia, arthritis. high inflammation parameters. cause unknown (viral infection in combination with the intake of anti-inflammatory drugs?).

Squamous cell carcinoma of the skin: chronically stationary (imperceptible growth) for 2 years, 1.5 cm large, painless, very firm ulcer with smooth edges on the underside of the tongue.

Psoriasis capitis: diffuse reddening of the entire capillitium with coarse lamellar scaling. Here in a 42-year-old patient with extensive psoriasis of the entire integument. Typically, the changes exceed the forehead-hairline.

stasis dermatitis: flat, sharply limited plaque of the entire right lower leg. lipofasciosclerosis in case of a previously known CVI with beginning papillomatosis cutis lymphostatica. condition after leg ulcer. currently distinct exudation, lymphorrhoea as well as secondary bacterial colonization.

Acanthosis nigricans: Bilateral greyish-brown, papillomatous-hyperkeratotic, asymptomatic, flat, rough plaques in a 40-year-old obese African-American patient.

Eczema, contact allergic eczema: proven nickel sensitization.

Sarcoidosis: anular or circulatory chronic sarcoidosis of the skin. persisting for several years. onset with small symptomless papules with continuous appositional growth and central healing. no detectable systemic involvement.

Lupus erythematodes chronicus discoides.

Stevens-Johnson syndrome: acute, extensive, painful erosions of the red of the lips, the lip mucosa, the tongue and the gingiva in an 18-year-old woman.

Candida sepsis: Oral mucosa of the previously described patient: Flat, thick, easily scraped off, whitish coating (base underneath slightly bleeding). Masses of C. albicans from oral mucosa swabs were culturally proven.

Lupus erythematodes chronicus discoides : Solitary blurred plaque with atropical surface, adherent scaling, bizarrely configured scarring (bright areas); distinct painfulness in case of punctiform exposure (e.g. brushing over with fingernail); unpleasant burning sensation when exposed to UV light.

Erythema anulare centrifugum: Characteristic single cell lesion with peripherally progressive plaque, which flattens centrally and is only recognizable here as a non raised red spot.

lupus erythematodes tumidus: chronic, relapsing disease pattern that has been active for months, completely without symptoms; succulent, surface-smooth, red plaques. high sensitivity to light. no hyperesthesia. ANA: negative; DIF: uncharacteristic. good response to antimalarial therapy.

Lichen sclerosus et atrophicus: Severe perianal and vulvar infestation with speckled pattern of sclerotic and atrophic areas.

Leukoplakia : Large cobblestone-like fielded leukoplakia of the tongue surface.