Splenic marginal zone lymphoma

被引:55
|
作者
Oscier, D
Owen, R
Johnson, S
机构
[1] Royal Bournemouth Hosp, Dept Haematol, Bournemouth BH7 7DW, Dorset, England
[2] Gen Infirm, HMDS Lab, Leeds LS1 3EX, W Yorkshire, England
[3] Taunton & Somerset Hosp, Dept Haematol, Taunton TA1 5DA, Somerset, England
关键词
splenic marginal zone lymphoma; splenic lymphoma with villous lymphocytes; clinical and diagnostic features; treatment;
D O I
10.1016/j.blre.2004.03.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
dSplenic marginal zone lymphoma (SMZL) is an indolent B cell malignancy usually involving spleen, bone marrow and blood. The disease presents as an incidental finding or with symptoms of splenic enlargement or anaemia. Diagnosis is based on a combination of lymphocyte morphology, immunophenotype and marrow and /or splenic histology. There is no genetic abnormality specific for SMZL, but SMZL cells may have either mutated or unmutated immunoglobulin variable region genes and probably arise from different subsets of splenic marginal zone B cells. Prognostic factors are poorly defined and only loss or mutation of the p53 gene is consistently associated with a poor outcome. Therapeutic options include splenectomy, splenic irradiation, alkylating agents, purine analogues or anti CD20 antibody. The median survival is 10-13 years and most disease-related deaths are associated with transformation to diffuse large cell lymphoma. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:39 / 51
页数:13
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