Image diagnoses for "Nodules (<1cm)", "red"
260 results with 810 images

Wickham's drawing: The stripes in each efflorescence appear as broad, white differently configured (also branched) lines; characteristic is the livid discoloration of the lichen planus (dermoscopic picture) .

Sweet syndrome: reddish-livid, succulent, pressure-dolent, infiltrated, solitary and partly papules confluent to plaques, on the right side of the body in a 47-year-old female patient. 1 week before the onset of the disease intake of Cotrimoxazol due to a urinary tract infection. temperatures > 38 °C.

Condylomata acuminata, perianal and extraanal soft cauliflower-like tumors.

Acne papulopustulosa: numerous inflammatory papules and pustules. few scars. numerous skin-coloured comedones

Candia-Balanitis: acute (within 1 day) after GM, itchy, flat erythema and plaques, papules and vesicles; healing within 1 week after consistent local antimycotic therapy.

Urticaria pigmentosa of childhood: extensive redness and urticarial reaction in the lesions after mechanical irritation.

Acne papulopustulosa: In acne typical distribution, red smooth and excoriated papules and some pustules.

Lichen planus classic type: for several months, red, itchy, polygonal, partially confluent, smooth, shiny papules that have remained in place for several months

Lichen planus classic type: for several weeks persistent, red, itchy, polygonal, partially confluent, smooth, shiny papules.

Acne infantum. 2-month-old girl, 2-4 mm in size, red, inflammatory papules and pustules (left front) in 2 months. At the edge of the picture on the right side a brownish, slightly sunken scar is visible. At the top center an older papule with scaly ruffle is visible (papule in healing).

Wrinkle treatment with filling materials: the ideal filling material is biocompatible, without allergenic potential, has a good long-term result, no side effects and a natural appearance. 8 weeks after injection of an unknown filling material, development of foreign body granulomas, which can be felt as solid deep conglomerates.

acrodermatitis papulosa eruptiva infantilis. exanthema of a few days old on the face, on the trunk (very discreet) and the extremities. disseminated, 0.2-0.4 cm large, red to reddish-brown papules with smooth surface. on the earlobe flat, succulent erythema with several, in places aggregated, rich red papules and vesicles.

Mucinosis follicularis type III: Chronic, often generalized, slightly itchy form in middle-aged to older adults, with disseminated, 0.1 cm large, skin-colored, red follicular papules on the trunk and extremities; possible precursor stage of folliculotropic mycosis fungoides (DD; type II of mucinosis follicularis; DD: malasseziafolliculitis).

Dermatitis, hypereosinophilic. partly papular, partly plaque-like, considerably itchy exanthema of disseminated, 0.3-1.5 cm large, red, smooth papules which have merged into an anular plaque formation on the buttocks.

Rosacea lupoide: non-itching, multiple, follicular yellow-brown papules that have existed for several months DD: demodex folliculitis can be ruled out

Lupus erythematodes chronicus discoides: succulent, hyperesthetic plaque with adherent scaling, 2.7x3.2 cm in size, existing for 4 months, no evidence of systemic LE. DIF with typical pattern.

Angiokeratoma scroti et vulvae. chronically stationary, multiple, bluish to dark black, 0.2-0.5 cm large, smooth symptomless vesicles. the clinical picture is diagnostically conclusive.

Transitory acantholytic dermatosis (M.Grover): a few weeks old, only moderately pruritic clinical picture with disseminated papules and also papulo vesicles; Nikolski phenomenon negative.

PEP. Severe itching, red papules on the trunk of a 26-year-old pregnant woman in the 3rd trimester.

Lichen planus exanthematicus: disseminated sowing of small red papules and confluent plaques.

Erythema perstans faciei. persistent, butterfly-shaped, livid red erythema in a 3-year-old boy with vitium cordis (pulmonary stenosis, subaortic stenosis, vascular transport and ventricular septal defect).

Neurofibroma in Type I Neurofibromatosis: Multiple Neurofibromas