Hidradenitis suppurativa, a progressive and extensive finding with papules, pustules, nodules and indurated ductal fistulae that has been present for many years.
Transitory acantholytic dermatosis (M.Grover): a few weeks old, only moderately pruritic clinical picture with disseminated papules and also papulo vesicles; Nikolski phenomenon negative.
Poikilodermia vascularis atrophicans: 72-year-old patient with a slowly progressive, varicolored-checked clinical picture of the skin, which has been present for > 15 years. the varicolored-checked skin is caused by reticular or stripe-shaped erythema and plaques. reticular or flat brown discoloration (hyperpigmentation) is also found. present is a "poikilodermatic mycosis fungoides".
Psoriasis vulgaris. psoriatic erythroderma. spread of psoriasis vulgaris as a maximum variant over the entire integument in the form of a generalised redness with scaling. rapidly spreading clinical picture; strong feeling of illness; high loss of fluid and temperature.
Pemphigus chronicus benignus familiaris: variable clinical picture with multiple, chronic, symptomless, scaly and crusty papules and plaques; section of a generalized clinical picture with typical infestation pattern.
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.
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.
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.
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.
Mammilla, accessory. 0.6 cm high, solitary, brown plaque, clearly grown during puberty, localized in the so-called embryonic lactiferous ridge, without symptoms, with a central pointed conical papule and a coarse-fielded surface.
scleroderma circumscripts (linear type): band-shaped expression of the scleroderma focus on the upper and lower leg. in the thigh area, clear atrophy of skin, subcutaneous fatty tissue (and muscles). clinical picture developed over a period of about 7 years. pulling and stabbing complaints during sports activities.
Nevus melanocytic more common: dermal n evoid melanocytes with monomorphic nucleus and only a few single nucleoli in here neuroid cytomorphological features with a wider pale eosinophilic cytoplasmic border
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