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Br J Dermatol ; 140(4): 708-14, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10233327

ABSTRACT

The term Richter's syndrome is used to describe the transformation of chronic lymphatic leukaemia (CLL) into a high-grade systemic lymphoma and is associated with a poor prognosis. We have undertaken detailed molecular studies in two patients with cutaneous B-cell lymphoma (CBCL) and CLL. Patient 1 exhibited a low-grade CBCL with different immunoglobulin gene rearrangements in blood and skin. By contrast, patient 2 showed identical gene rearrangements, confirmed by gene sequencing, and died within 4 months of presentation. The latter patient fulfilled the criteria for a diagnosis of cutaneous Richter's syndrome, whereas the former patient demonstrated the coincidence of CLL with a primary CBCL. Our results highlight the importance of gene rearrangement studies with sequencing for the accurate diagnosis of cutaneous Richter's syndrome.


Subject(s)
Leukemia, Lymphocytic, Chronic, B-Cell/complications , Lymphoma, B-Cell/complications , Skin Neoplasms/complications , Aged , Female , Gene Rearrangement/physiology , Genes, Immunoglobulin/physiology , Humans , Leukemia, Lymphocytic, Chronic, B-Cell/immunology , Leukemia, Lymphocytic, Chronic, B-Cell/pathology , Lymphoma, B-Cell/immunology , Lymphoma, B-Cell/pathology , Male , Skin Neoplasms/immunology , Skin Neoplasms/pathology
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