Malformations, syndromal, vascular. mixed, syndromal, capillary/venous/arterial malformation with arterio-venous anastomoses and reactive hyperplasia of the tissue (Klippel-Trénaunay syndrome).
Cheilitis granulomtosa: Monosymptomatic orofacial granulomatosis. solitary, chronically dynamic, recurrent for months, markedly increased in consistency, indolent, red, smooth swelling of the lower lip. no lingua plicata. no facial paresis.
Erysipelas, acute: Acute reddened and painful, large-area, succulent plaque, only blurredly limited, which has existed for 5 days and is accompanied by high fever; inflammation parameters massively increased.
Acute paronychia: blistery, circumferential, painfully throbbing paronychia (bulla repens) that has been present for a few days, caused by poygenic cocci.
Erysipelas, acute: under high fever, , within 2 days appeared, sharply limited flat, saturated redness and plaque formation of the left buttock. accompanying: painful regional lymphadenitis.
Fasciitis, necrotizing. foudroyant running, primarily underestimated, highly painful clinical picture with high fever and massive swelling of the left hand. Patient with several years of immunosuppressive therapy.
Infection of the foot, gram-negative, painful macerations on toes and ball of the foot, sharply defined, whitish maceration on the edge, spotted fibrinous and purulent towards the depth, foul-smelling, evidence of Pseudomonas aeruginosa.
Cheilitis granulomatosa. 3-year-old disease symptoms. solitary, chronically dynamic, initially variable, for half a year permanent, clearly increased in consistency, indolent, red, smooth swelling of the upper lip and the adjacent cheek areas. no lingua plicata.
Melkersson-Rosenthal syndrome (monsymptomatic form; here Blepharitis granulomatosa): initially recurrent, now permanent swelling of the left upper lid; no lingua plicata; no neurological symptoms.
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