| Literature DB >> 10838457 |
J Várkonyi1, A Zalatnai, J Timár, A Matolcsi, A Falus, M Bencsáth, V László, E Pócsik, B Kotlán, A Császár.
Abstract
We describe a patient presenting with B cell chronic lymphocytic leukemia (B-CLL) who subsequently developed cutaneous infiltrates. Specimens of the blood, bone marrow and cutaneous infiltrations all showed the same heavy-chain gene rearrangement. Following failure of conventional chemotherapy, and in view of the similarity of the disease to cutaneous T cell lymphoma, interferon-alpha therapy was employed with satisfactory results. Introduction of this cytokine to the therapeutic modalities for secondary cutaneous B-CLL would hopefully change the poor outcome of this entity, or at least could produce a better quality of life. Loss of histidine decarboxylase activity in the infiltrating cells - in contrast to circulating lymphocytes - may be associated with the transformation of B-CLL to a more aggressive infiltrative form, offering a possible explanation for tissue invasiveness. The changing character of the disease raises the possibility of a second mutational event in the course of B-CLL. Copyright 2000 S. Karger AG, BaselEntities:
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Year: 2000 PMID: 10838457 DOI: 10.1159/000041031
Source DB: PubMed Journal: Acta Haematol ISSN: 0001-5792 Impact factor: 2.195