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A Case of Lymphomatoid Papulosis after Allogenic Bone Marrow Transplatation
Korean Journal of Hematology ; : 111-115, 2005.
Article Dans Coréen | WPRIM | ID: wpr-720499
ABSTRACT
A twenty-year-old man developed pruritic papules on his right forearm on the 25th day after an allogeneic bone marrow transplantation from an HLA-matched related donor. The skin lesion turned out to be lymphomatoid papulosis, both histologically and immunophenotypically, not a GVHD skin lesion. Lymphomatoid papulosis is a chronic lymphoproliferative disease of the skin, characterized by recurrent crusts of pruritic papules, which initially appearing on the upper trunk and both extremities. The lesions heal spontaneously within 2~8 weeks, usually leaving slightly depressed oval scars. Histologically, the lesions show wedge-shaped dense dermal infiltrates of lymphoid cells, with numerous eosinophils, neutrophils and atypical lymphocytes. As much as 50% of the infiltrates show atypical lymphocytes, and the dermal vessels may show endothelial swelling, fibrin deposition and red blood cell extravasation. We are reporting a case of spontaneously healing CD56+ lymphomatoid papulosis, in the patient who received bone marrow transplantation, is reported.
Sujets)

Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Peau / Donneurs de tissus / Moelle osseuse / Fibrine / Lymphocytes / Transplantation de moelle osseuse / Cicatrice / Papulose lymphomatoïde / Granulocytes éosinophiles / Érythrocytes Limites du sujet: Humains langue: Coréen Texte intégral: Korean Journal of Hematology Année: 2005 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Peau / Donneurs de tissus / Moelle osseuse / Fibrine / Lymphocytes / Transplantation de moelle osseuse / Cicatrice / Papulose lymphomatoïde / Granulocytes éosinophiles / Érythrocytes Limites du sujet: Humains langue: Coréen Texte intégral: Korean Journal of Hematology Année: 2005 Type: Article