Graft-versus-host disease, chronic: about 2 years after stem cell transplantation, generalized, lichenoidal partly soliltary, partly confluent red-brown paques, moderate itching.
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.
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.
Graft-versus-Host-Disease: brownish pigmented, partly also scleroderma-like skin changes in the area of the forearm and hand, approx. 6 months after bone marrow transplantation.
Graft-versus-Host-Disease: brownish pigmented, reticular spots on both upper arms.
Graft-versus-Host-Disease: brownish pigmented, partly also scleroderma-like skin changes on both thighs. Approx. 12 months after bone marrow transplantation.
Graft-versus-Host-Disease: brownish pigmented, partly also scleroderma-like skin changes on both legs, approx. 12 months after bone marrow transplantation.
Graft-versus-host disease, chronic: about 2 years after stem cell transplantation, generalized, lichenoidal partly soliltary, partly confluent red-brown paques, moderate itching.
Graft-versus-host disease, chronic: about 2 years after stem cell transplantation, generalized, lichenoidal partly soliltary, partly confluent red-brown paques, moderate itching.
Graft-versus-Host-Disease, chronic. about 1.5 years after a stem cell transplantation, extensive hardening with irregular brownish pigmentation. considerable restriction of movement.
Interface dermatitis with atrophy of the surface epithelium, orthokeratosis and a thin lichenoid infiltrate in the upper dermis.
Graft-versus-host disease; detail of the picture; atrophic epithelium, orthokeratosis, edema of the upper dermis, lichenoid infiltrate with vacuolic degeneration of basal epithelia; individual dyskeratoses.
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