T-cell prolymphocytic leukemia: A report of two cases with review of literature

被引:2
|
作者
Naseem S. [1 ]
Gupta R. [2 ]
Kashyap R. [1 ]
Nityanand S. [1 ]
机构
[1] Department of Hematology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh 226 014, Raebarelli Road
[2] Dr B R A IRCH, All India Institute of Medical Sciences Absari Nagar
关键词
Immunophenotyping; Prolymphocyte; T-PLL;
D O I
10.1007/s12288-008-0043-6
中图分类号
学科分类号
摘要
T-cell Prolymphocytic Leukemia (T-PLL) is a mature post-thymic T-cell malignancy with aggressive clinical course. The principal disease characteristics are organomegaly, skin lesions and raised lymphocyte counts. We report two cases of T-PLL. T-PLL is a rare T-cell malignancy with characteristic clinical and laboratory features and a poor prognosis. It needs to be differentiated from B-Cell prolymphocytic leukemia (B-PLL) and other mature T-cell lymphoproliferative disorders with predominant leukemic pattern. Differentiation can be made by a comprehensive approach taking into account the clinical features, the cell morphology and the immunophenotype of leukemic cells. © Indian Society of Haematology & Transfusion Medicine 2008.
引用
收藏
页码:178 / 181
页数:3
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