Image diagnoses for "Plaque (raised surface > 1cm)", "Face"
114 results with 290 images

psoriasis vulgaris. seborrhoid psoriasis. large, flat, red, rough plaques with fine-lamellar scaling, localized by the centrofacial system, appearing in a 26-year-old woman. similar skin changes were found on the trunk and the extensor extremities. relapsing course of the disease since adolescence.

Lupus erythematodes chronicus discoides , chronic moderately indurated plaques, marginal with inflammatory activity, central scarring.

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.

Acne conglobata: Condition following acne conglobata with scars and scar strands that have sunk in teisl, sometimes bulging and disfiguring.

Psoriasis seborrhoeic type: for several months, symmetrical, only slightly elevated, homogeneously filled red-yellow, slightly accentuated, scaly plaques, which have remained in the same place for several months, with red lips.

Lupus erythematodes chronicus discoides: characteristic focus at the temple.

AIN: perianally localized, less sympotmatic, extensive, whitish erosive plaque at 3 o'clock; secondary findings anal fissure at 6 o'clock (actual cause of the doctor's visit)

Lupus erythematodes chronicus discoides: cutaneous chronic lupus erythematosus. years of course with circumscribed red scarring plaques (circle - with whitish atrophic area without follicular structure): arrow: dermal melanocytic nevus.

Initial findings (see following figure) 7 years later.

Type I leprosy reaction "upgrading reaction": in a patient with Boderline lepromatous leprosy, characterized by an inflammatory flare-up of facial plaques.

Dermatitis, seborrheic: Blurred, delicately reddened, coarse lamellar scaling, flat, slightly infiltrated plaques in a 24-year-old female patient.

Mixed connective tissue disease: 43-year-old female patient (with clinical aspect of systemic lupus erythematosus) who fulfils the criteria of MCTD: U1.nRNP : titre : >1:1600; characteristics of systemic lupus erythematosus, Raynaud's phenomenon, swollen hands as well as feeling ill, fatigue, proximal muscle weakness (typical myositis symptoms).

Dermatitis, seborrhoeic. 6-month-old female patient with almost symmetrical, blurred, flatly infiltrated, scaly, non-itching red plaques. good clinical response to steroidal pre-treatment. recurrence of skin symptoms within a few days after discontinuation of therapy.

Acute erysipelas. acutely appeared, since a few days existing, increasing, flat, sharply defined, pillow-like raised, flaming red and painful swelling of the cheek and the left eye. distinct impairment of the general condition with fever.

Dyskeratosis follicularis (Darier's disease) Disseminated, yellow-brownish papules and plaques, sometimes covered with small crusts.

Acne papulopustulosa:Multiple, inflammatory papules and pustules, some of them crusty, localized periorally and perinasally in the face of a 16-year-old adolescent.