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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Utikal, J; Ugurel, S; Kurzen, H; Erben, P; Reiter, A; Hochhaus, A; Nebe, T; Hildenbrand, R; Haberkorn, U; Goerdt, S; Schadendorf, D.
Imatinib as a treatment option for systemic non-Langerhans cell histiocytoses.
Arch Dermatol. 2007; 143(6):736-740 Doi: 10.1001/archderm.143.6.736 (- Case Report) [OPEN ACCESS]
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Co-Autor*innen der Med Uni Graz
Ugurel-Becker Selma
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Abstract:
Background: Systemic non-Langerhans cell histiocytoses are disorders characterized by the accumulation of histiocytes that do not meet the criteria for Langerhans cells in various organs. So far, no causative treatment is known. Observations: Herein, we report the case of a 41-year-old man with Rosai-Dorfman disease, a form of systemic non-Langerhans cell histiocytoses, with histiocytic infiltrations in the skin, bone marrow, liver, and spleen. Histiocytes were positive for the imatinib target proteins platelet-derived growth factor receptor 0 and KIT. The disease completely responded to treatment with 400 to 600 mg daily of imatimb for more than 7 months. Conclusion: This case shows that imatimb is a powerful treatment option for patients with non-Langerhans cell histiocytoses.
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