Image diagnoses for "Plaque (raised surface > 1cm)"
591 results with 2936 images

Dermatosis acute febrile neutrophils: Findings in the legs.

Pemphigus erythematosus (state after UV-provocation): since about 2 years recurrent, symmetrical skin changes localized in the seborrheic areas. After pretreatment flat depigmentations so oral, scaly palques. On the lower left side the UV-provoked square area (isomorphic irritant effect).

Psoriasis guttata: acutely and de novo appeared, 0.1-2.0 cm large, reddish, rough papules and plaques with fine-lamellar scaling on the trunk and extremities in a 24-year-old woman. A feverish streptococcal angina preceded this. After healing of the initially manifested symptoms, a longstanding chronic, intermittent course of psoriasis followed.

Candida granuloma. chronic recurrent nodular cutaneous-subcutaneously localized, deep-reaching, livid inflammatory foci on the wrist of an immunocompromised, 28-year-old patient. abundant C. albicans detectable in the smear. development of new nodules despite oral antimycotic medication. partial healing leaving post-inflammatory pigmentation.

Rowell's syndrome: acute "multiform" exanthema in subacute cutaneous lupus erythematosus.

Naevus, melanocytic, congenital. congenital, painless, not actively growing, slightly raised, moderately consistency increased, sharply defined, brown, smooth plaque.

Cheilitis simplex: DD: actinic cheilitis

Keratosis lichenoides chronica: generalized eminently chronic, moderately itchy clinical picture with reddish, firm, papules and plaques with scaling.

Leprosy (overview): Borderlinelepromatous leprosy (BB), plaques and dome-shaped punch-out lesions.

Pemphigoid gestationis. itchy, since 4 weeks existing exanthema with multiple, generalized, symmetric, truncated, large red plaques with isolated, bulging blisters. picture reminds of an erythema exsudativum multiforme.

Balanitis plasmacellularis: chronic balanitis in a 62 year old patient. no other skin diseases known. no diabetes mellitus. slight urinary incontinence in case of prostate hyperplasia. sharply defined, slightly raised red plaque. no significant symptoms.

AIN. Anal dysplasia. Large, hyperkeratotic area with smaller satellite lesions. The surface is granular and shows different areas of keratinization. Histologically, there was a grade 2 intraepithelial neoplasia.

Lichen planus verrucosus: a hypertrophic lichen planus with pseudoepitheliomatous epithelial hypertrophy and scarring that has been present for several years.

Tinea corporis. multiple, chronically active, grouped, 0.5-10.0 cm large (or larger), isolated and confluent, moderately to distinctly itchy, slightly rimmed, rough, scaly bright spots (and plaques). slow growth of single florets.

Leiomyoma. Close up of the multiple leiomyomas described above.

Primary cutaneous follicular center lymphoma: chronically active, increasing for 12 months, localized on the trunk and upper extremities, disseminated, 0.3-0.7 cm in size, asymptomatic, hemispherical, firm, smooth, red papules and nodes.

For a long time now, this large, "well-cared for", low-consistency, borderline, sometimes itchy plaque (interval-like local treatment with corticosteroids) has existed in the 42-year-old patient.

Erythrokeratodermia progressiva symmetrica. extensive, sharply defined, brown-yellow discoloured, scaly and hardened plaques existing since the 2nd LJ, which had already appeared on other parts of the trunk, but healed there in the meantime. occasional slight itching.

Lichen sclerosus extragenitaler: Progressive lichen sclerosus for 2 years with a clearly sunken scarring of the lower lip and chin; surrounding, flat, blurred, clearly consistent plaque with a red-white coloration in the chin area (here the clinical features of the lichen sclerosus are visible).