Image diagnoses for "Plaque (raised surface > 1cm)"
597 results with 2952 images

mixed connective tissue disease: 53-year-old female patient. known for several years raynaud syndrome. episodes have become more frequent in recent months. for about 3 months, increasing fatigue, lack of drive and strength, joint pain intensified in the morning, swelling of the hands and fingers (sausage fingers). ANA: 1.1280; U1RNP antibodies+.

Mixed connective tissue disease: stripy livid erythema on the back of the hand and the back of the fingers, collagenosis hand.

Lymphoma, cutaneous B-cell lymphoma, marginal zone lymphoma. Detailed picture: red, surface smooth papules and plaques in a 59-year-old patient. No scratch excoriations, no scaling, no pruritus.

Primary cutaneous marginal zone lymphoma: 10 monthsago , first appearance of red, surface smooth papules and plaques in a 59-year-old patient; no scratch excoriations, no scaling, no pruritus.

Lymphoma cutaneous B-cell lymphoma Plasmocytoma: subcutaneous and cutaneous nodules taken from: Santos G et al (2014) An Bras Dermatol 89:173-174

Primary cutaneous diffuse large cell B-cell lymphoma leg type: Survey image : Since about 12 months persistent, slowly progressing, about 4-5 cm in diameter, irregularly shaped, bulging, deep red tumor with smooth surface in a 75-year-old patient with a central atrophic, scar-like aspect.

Primary cutaneous diffuse large-cell B-cell lymphoma leg type: Detail magnification: Approx. 4-5 cm diameter, irregularly shaped, bulging, deep red tumor with smooth surface of a 75-year-old patient.

primary diffuse diffuse large cell B-cell lymphoma leg type: for about2 years papules and nodules on the left leg of a 55 years old woman appearing in relapses. in the last weeks rapid growth of the pre-existing nodules and eruptive appearance of new nodules. initially no symptoms. since 2 months increasing tendency to dry and also weeping surface scaling. in places complete decay of the nodules.

Primary cutaneous diffuse large cell B-cell lymphoma leg type: since 6 months existing, steadily growing, not painful conglomerate, moderately consistency increased red surface smooth nodule, no systemic involvement proven, therapy: excision.

Primary cutaneous diffuse large cell B-cell lymphoma leg type: For about 2 years papules and nodules on the left leg of a 55 years old woman appearing in relapses. In the last weeks rapid growth of the pre-existing nodules and eruptive appearance of new ones. Initially no symptoms. For 2 months increasing tendency to surface scaling and ulcer formation.

parapsoriasis en plaques, benign small hereditary form. 55-year-old patient with small spotted parapsoriasis en plaques (also called chronic superficial dermatitis). the distribution pattern (fingerprint dermatosis) in the longitudinal direction of the skin tension lines is almost diagnostic. occasionally slight itching (mostly in the winter months). in summer (after sea vacation) almost healed. histology is often not conclusive.

Parapsoriasis en plaques large-heart poikilodermatic: a sympothless, slowly progressive clinical picture that has existed for several years, with poikilodermatic changes consisting of reticular lichenoid, pityriasiform scaling, papules and plaques and central atrophy of the skin.

Pityriasis rosea. truncated, in the skin tension lines arranged (see following figure), thick maculopapular exanthema, little itching.

Pityriasis rosea. close-up: Disseminated, up to 2.0 cm large, in places strongly scaling papules and plaques; arrangement in the skin cleft lines.

Pityriasis rubra pilaris (adult type): Sharply set off towards the wrist (difference to hyperkeratotic palmar eczema), alternating, flat palamarkeratosis.

Pityriasis rubra pilaris (adult type) Detail: chronic recurrent course for years with phases of marked improvement and extensive recurrence (fig. in a relapse period). Characteristic for the disease are the boundaries of the plaques drawn with a sharp pencil, resulting in the so-called "nappes claires", sharply recessed zones of unaffected skin in the case of extensive infestation.

Pityriasis rubra pilaris (adult type) Detailed view: chronic recurrent course for years with phases of marked improvement and extensive recurrence (fig. in a thrust period).

Papillomatosis cutis lymphostatica. massive findings with papillomatous vegetation on the back of the foot and toes. condition after recurrent erysipelas.

Papillomatosis cutis lymphostatica 14 days after keratolytic therapy.

Papillomatosis cutis lymphostatica: Large-scale verrucous plaque with a blurred border on all sides, coarsely indurated, with formation of succulent nodules; condition following recurrent erysipelas.

Pemphigoid gestationis: Intensely itching exanthema since 4 weeks with multiple, generalized, symmetrical, truncated, large red plaques with isolated, bulging blisters.

Impetigo contagiosa. red, erosive, rough, partly crust-covered plaque with rhagades and scaly crusts, persistent for several weeks, resistant to therapy. evidence of Staphylococcus aureus.

Keratosis palmoplantaris papulosa seu maculosa. since earliest childhood known keratosis anomaly of the hands (here less conspicuous) and feet, which is not disturbing so far. multiple, differently sized, wart-like horny cones with rough, scaly surface.

PEP: multiple, massively itchy urticarial papules, also papulo vesicles; firstborn, last trimester pregnancy.

PEP: Atypical minus variant with few, clearly itchy, umbilical and periumbilical scaly plaques Note: the periumbilical region is often not markedly affected (DD: pemphigoid gestationis)