Image diagnoses for "Macule"
321 results with 1208 images

Lichen sclerosus of the vulva: pronounced smooth whitish sclerosis of the vulva and penineum; extensive atrophy of the small labia with gaping vagina. 7-year-old girl; changes of the lichen sclerosus for several years.

Vitiligo.

Physiological tanning by solarium, reduced pigmentation at the contact points.

Chronic light damage: poikiloderma after years of excessive UV exposure, including hyperpigmentation, depigmentation and numerous precanceroses of the actinic keratosis type.

Naevus flammeus: congenital, completely symptomless vascular malformation (exclusively capillary malformation) without tendency to tissue hypertrophy.

Raynaud's phenomenon:Raynaud's syndrome known for several years. No indication of systemic scleroderma. Here condition after Raynaud's attack with massive blue discoloration of the fingers.

Vascular (capillary) malformation (so-called naevus flammeus): Congenital, generalized, spotty erythema from the scalp to the sole of the foot in an 8-year-old boy, developed according to age.

DD: Rosacea erythematosus- here lupus pernio: 63-year-old female patient with reddish-livid plaque of the nose and previously known chronic pulmonary sarcoidosis.

Purpura thrombocytopenic: line shaped (after scratching, as well as after application of a compression bandage) fresh and slightly older skin bleedings (cannot be pushed away diascopically).

Dermatitis perioralis, granulomatous type. multiple, chronically dynamic, continuously increasing for 3 months, periorally localized, disseminated, follicular, firm, itching and burning, red, rough, scaly papules, pustules and plaques. months of pre-treatment with corticoid ointments!

Melanoma, malignant, lentigo-maligna melanoma. deep black, irregularly limited, asymmetrical plaque in the facial region. on the right medial side an almost skin-coloured verruca seborrhoica.

Purpura fulminans: Purpura fulminans beginning in the abdominal region in the context of E. coli sepsis in a 55-year-old man (lethal outcome).

Chloasma gravidarum perstans: Chronic stationary, no longer increasing, smooth, brown spots located in the temporal region in a 29-year-old woman 14 months after delivery.

Nevus flammeus: congenital, asymmetrically arranged, non-syndromal (no tissue hypertrophy, no orthopedic malposition) large-area (telangiectatic) vascular nevus; characteristic are the scattered borders of the red spots.

Hyperpigmentation, post-inflammatory. acutely occurring asymptomatic brown-black hyperpigmentation of the gingiva in an African after gingivitis.

lupus erythematosus acute-cutaneous: acute symmetrical skin symptoms after sun exposure, which have persisted for 1 week. pat. was previously free of skin symptoms. clear feeling of tension in the skin. laboratory: ANA+; anti dsDNA antibodies neg.; anti-Ro antibodies positive.

Vitiligo. solitary or multiple, white, hypopigmented, sharply defined patches. shown here is a detailed picture. further patches were found on the neck region, hands, axillary region, nipples, navel, genito anal region.

Klippel-Trénaunay syndrome: extensive vascular malformation with extensive nevus flammeus affecting the trunk, the right arm and both legs. No evidence of soft tissue hypertrophy so far. No AV fistulas.

Livedo racemosa generalisata: extensive, bizarre, haemorrhagic reticulation of the skin