Granuloma anulare erythematous type. little indurated, marginal reddish-brown plaque with indicated central atrophy. slow centrifugal growth lasting for months. Granulomatosis disciformis chronica et progressiva is to be considered as a differential diagnosis (entity).
Lymphoma cutaneous NK/T-cell lymphoma nasal type: ulcer covered with red granulation tissue and crusts that has been expanding for months with partial destruction of the nasal septum.
Purpura thrombocytopenic: acutely occurring, partly large-area, partly punctiform, non-anemic spots with a tendency to confluence; sudden onset with fever, multiple thromboses, disorientation, stupor; it is a drug-induced form of thrombotic thrombocytopenic purpura with hemolytic microangiopathic anemia at the base of an infectious disease and a previously unknown drug allergy.
Morbihan, M.. overview: Chronic persistent swelling of the right half of the face, especially of the upper eyelid and the periorbital region in a 30-year-old man which has persisted for about 1.5 years.
Nummular Dermatitis: General view: For 3 years persistent, itchy, eroded, excoriated, partly encrusted, coin-shaped plaques on the left lower leg of a 64-year-old female patient.
Nevus flammeus (port wine stain): congenital erythema in the facial region (capillary vascular malformation), localized in V2 distribution, completely without symptoms; control image after 4 years
Eczema atopic (overview): severe, universal (erythrodermic) atopic eczema. exacerbation phase since about 3 months. patient with rhinitis and conjunctivitis in pollinosis. total IgE >1.000IU.
Prurigo simplex subacuta:0.3-0.4 cm large, red, centrally eroded or ulcerated, moderately sharply defined, interval-like, violently itching papules, which are shown in the present image detail in different stages of development.
Keloids: Flat, smooth-surfaced, firm, red nodules, increased vascular drawing. In this clinical picture a dermatofibrosarcoma protuberans can be excluded by differential diagnosis.
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