Image diagnoses for "Skin defects (superficially, deep)"
166 results with 437 images

Erythema multiforme: suddenly occurring, itchy, disseminated exanthema with cocard-like plaques which has been present for 4 days. here the finding on the lower leg. striated arrangement after external stimulus. s. isomorphism (Koebner phenomenon).

Eccema herpeticatum, densely aggregated, grouped, centrally navelled vesicles and eroded papules.

Ulcus cruris venosum, localised at a typical site (ankle region), large, moderately painful ulcer covered with fresh granulation tissue.

Zoster mucosae: unusually localized zoster disease of the buccal mucosa.

Interdigital candidiasis, also called erosio interdigitalis blastomycetica.

Merkel cell carcinoma: uncharacteristiccentrally deep ulcerated, plate-like lump, previously calotte-shaped growth.

Aromatase inhibitors: severe leukocytoclastic vasculitis under therapy with an aromatase inhibitor (taken from: Woodford RG et al. 2019)

Artifacts.

Gingivostomatitis, chronic. sharply defined, chronically stationary, burning redness in the area of the contact surfaces of the dental prosthesis. this has resulted in hyperplastic-papillomatous epithelial hyperplasia (palatal papillomatosis). the hard palate and the alveolar processes in the upper jaw are typical localisations affected here.

Lichen planus erosivus mucosae. painful gingivitis existing for more than one year. altogether progressive course. chronic stationary, border-like, painful erythema and extensive erosions can be found

Syphilis acquisita:painless, very coarse primary effect of the upper lip, 3 weeks after suspicious sexual contact. Considerable firm swelling of the upper lip. Clear, non-painful adenopathy of the submandibular lymph nodes.

Lichen planus mucosae: erosive Lichen planus mucosae with painful erosive cheilitis.

Zoster:Severe, not quite fresh necrotizing zoster with deep scarring. HIV infection.

Ulcer of the skin: complete necrosis of the end phalanx in previously known psoriatic systemic scleroderma.

Fasciitis, necrotizing. Foudroyante, extensive defect formation.

Gingivostomatitis, chronic. chronic dynamic, variable, 1.4 cm large, dolent, bizarrely configured ulcer in a 64-year-old female patient with Huntington's disease. development due to ulcerative inflammation at the left lateral edge of the tongue. massive plaque accumulation and sharp-edged incisal and occlusal surfaces have promoted the inflammatory process.

Stevens-Johnson syndrome: acutely occurring, extensive, painful erosions of the red of the lips, the mucous membrane of the lips and the tongue in a 22-year-old man.

Stevens-Johnson syndrome: acute with accompanying fever, occurred extensive, painful erosions of the red of the lips, lip mucosa and tongue in a 17-year-old woman. A few days later multiromic exanthema of the runp and face. The cause was probably the intake of ibuprofen.

Pyoderma gangränosum. initial findings lasting for years with therapy resistant ulcers. hypertrichosis after several months of unsuccessful therapy with cyclosporine.