Image diagnoses for "Hardening (cutis, subcutis - nodular/plate-like)"
55 results with 128 images

Dermatoliposclerosis. 64-year-old female patient with known CVI. For years increasing hardening of the distal and middle third of the US (so-called bottle bone). Extensive hyper - and depigmentation of the skin with wood-like, coarse increase in consistency.

Scleroderma en coup de sabre: hairless porcelain-like plaque that has been growing for years.

Mondor's disease: suddenly appeared, strand-like, about 7 cm long, firm, only slightly pain-sensitive induration; no underlying disease known.

Mondor disease: explanatory detail.

Scleromyxoedema: Multiple, symmetrically distributed, 0.1-0.2 cm large, roundish, non follicular papules with smooth, shiny surface.

Scleromyxoedema: waxy, flat hardened palms; changes can be detected mainly on the fingers and over the finger base joints.

Long-standing lichen sclerosus of the vulva with complicated carcinoma development (see following figure); complete atrophy of the small labia.

Chronic radiodermatitis: Condition following radiation of a bronchial carcinoma.

Hypodermitis: extensive reddening and induration of the lower leg. Painful if finger pressure is applied firmly. The tissue can be dented by prolonged finger pressure.

Cheilitis granulomatosa with pearlèche.

Papillomatosis cutis lymphostatica:large-area, distally sharply defined, proximally tapering, coarsely indurated, large-area, verrucous plaque with smaller nodules; condition following recurrent erysipelas.

Graft-versus-Host Disease: extensive scleroderma indurations of the arms and legs.

Generalized GVHD: chronic, generalized, poikilodermatic skin changes, with circumscribed calluses, atrophy and reticular hyperpigmentation.

Lichen sclerosus et atrophicus: massive infestation of the vulva with bulging sclerosing of the labia majora and labia minora, first changes had occurred 10 years ago.

Hidradenitis suppurativa, a widespread and progressive condition with papules, pustules, nodules, indurated, ductal fistulae and consecutive chronic lymphedema.

Scleroderma ligamentous: for years slowly progressive, only moderately indurated ligamentous morphea in a 42-year-old woman; no movement restrictions of the joints.

Scleroderma ligamentous: for years slowly progressive, only moderately indurated ligamentous morphea in a 42-year-old woman; no movement restrictions of the joints.

Graft-versus-Host-Disease. 12 months after transplantation, reaction due to transmission of allogenic immunocompetent T-lymphocytes. extensive dermatosclerosis with numerous, bizarre, skin-coloured papules and plaques.

Lichen sclerosus of the vulva: verrucous lichen sclerosus with synecchia between small and large labia, extensive atrophy of the small labia with narrowing of the introitus vaginae.

POEMS syndrome: flat, even hyperpigmentation with "scleroderma-like" hardening and swelling of the forearm and back of the hand.

Scleroderma, systemic: taut, shiny facial skin (see chin region); distinct perioral fibrosis, which becomes clearly visible when the lips are tapered.

Scleroderma, systemic (sclerosis of the hands): Raynaud's syndrome, known since puberty, palmar hyperhidrosis, slight doughy swellings with reduced skin shifting; sclerosis becomes apparent when the fingers are simply bent.

Bilateral varicosis: trunk varicosis of the V. saphena magna; pronounced CVI of both lower legs.

Venous insufficiency chronic: pronounced congestive dermatitis with extensive induration of both lower legs.

Laser scanning microscopy: Subepithelial, band-shaped homogeneous swelling zone of collagenous connective tissue, isolated inflammatory cells