Image diagnoses for "Hardening (cutis, subcutis - nodular/plate-like)"
53 results with 126 images

Graft-versus-host disease. 3-15 months after transplantation, a reaction due to the transmission of allogenic immunocompetent T-lymphocytes. extensive dermatosclerosis with numerous, bizarre, skin-coloured papules and plaques.

Lymphoma, cutaneous T-cell lymphoma, panniculitis-like acute clinical picture with plate-like infiltrates, which receded leaving behind deep and extensive scarring of skin and subcutis.

Panniculitis, pancreatic. Proven lobular panniculitis with known chronic pancreatitis.

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

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.

Scleroderma circumscripts: Band-like form of the scleroderma focus on the upper and lower leg. clinical picture that developed slowly over a period of about 7 years. pulling and stabbing complaints during sports activities.

AL-amyloidosis in smoldering myeloma: In the 77-year-old patient, this macroglossia with lingua plicata, which has been steadily increasing for 1 year, is clinically present with recurrent flat ecchymoses of the periorbital region, corresponding to a hematoma of the eyeglasses. Further purple skin changes are present in the neck and retroauricularly. The bone marrow biopsy revealed smoldering myeloma (degree of infiltration of plasma cells at 15%).

Keratosis extremitatum hereditaria transgrediens et progrediens

Keratosis extremitatum hereditaria transgrediens et progrediens

Keratosis extremitatum hereditaria transgrediens et progrediens

Foreign body granuloma: after injection of "filler material

Graft-versus-Host-Disease, chronic. 2 years after stem cell transplantation, large-area scleroderma and poikiloderma skin changes. here detail picture with massive acrosclerosis. scarring of the fingertips after healed fingertip necrosis.

Graft-versus-Host Disease, chronic: 1.5 years after stem cell transplantation, large-area scleroderma with significant movement restriction, significant reduction of the AZ

Kraurosis vulvae: Manifestation of a lichen sclerosu of the vulva (small and large labia, clitoris, introitus vaginae) with pronounced atrophy of the external genitals (clinical picture used to be separated from the lichen sclerosus et atrophicus as an independent clinical picture)

Circumscribed scleroderma (generalized plaque type): almost universal infection of the integument; typical of circumscribed scleroderma is the recess of the nipples and the perimamillary region.

Scleroderma circumscripts (plaque type; pattern of phylloid cutaneous mosaic - see below mosaic dermatosis acquired)

Generalized circumscribed scleroderma: large-area evenly indurated sclerosis of the skin, skin with a shiny, reflective surface.

scleroderma circumscripts (plaque type). large, map-like bizarrely limited, brown, smooth plaques. no recognizable inflammatory symptoms. there is no feeling of tension. no pain. comment: apparently largely aphlegmatic (healed) scleroderma.

Morphea type or plaque type of circumscribed scleroderma: slightly idurated irregularly bordered white plaque with a parchment-like, scale-free surface; discreet, light red rimythema.

Scleromyxoedema. 52-year-old patient. Continuously increasing, moderately itchy skin lesions for 5 years.

Scleromyxedema. 52-year-old patient shows a diffuse thickening and discreet reddening of the facial skin. Especially in the area of the glabella there is a bulging overlapping thickening of the skin folds.

AL-type amyloidosis: lingua plicata in macroglossia and systemic AL-type amyloidosis.

Lichen sclerosus of the vulva: pronounced smooth whitish sclerosis of the vulva and penineum; extensive atrophy of the small labia with gaping vagina. 7-year-old girl; changes of the lichen sclerosus for several years.

Lymphoma cutaneous T-cell lymphoma panniculitis-like: circumscribed, rather inconspicuous, moderately painful, red, in places ulcerated and clearly indurated plaque.

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