CHRONIC LYMPHOPROLIFERATIVE DISORDERS - CLASSIFICATION AND DIAGNOSIS

被引：16

作者：

LITZ, CE ^{[1
]}

BRUNNING, RD ^{[1
]}

机构：

[1] UNIV MINNESOTA HOSP & CLIN,MINNEAPOLIS,MN 55455

来源：

BAILLIERES CLINICAL HAEMATOLOGY | 1993年 / 6卷 / 04期

关键词：

D O I：

10.1016/S0950-3536(05)80175-1

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

The chronic lymphoproliferative disorders are morphologically, immunologically and clinically heterogeneous. Common features of these processes include T, B or natural killer cell immunophenotypes and terminal deoxynucleotidyl transferase negativity. The B cell lymphocytic disorders include B-chronic lymphocytic leukaemia, B cell prolymphocytic leukaemia, chronic lymphocytic leukaemia-prolymphocytic leukaemia, non-Hodgkin's lymphoma (including mantle cell lymphoma) in leukaemic phase, hairy cell leukaemia and splenic lymphoma with villous lymphocytes. The T cell chronic lymphoproliferative disorders include prolymphocytic leukaemia, adult T cell leukaemia-lymphoma, large granulated lymphocyte leukaemia and Sézary syndrome. Occasionally, a lymphocytic proliferation is encountered that does not satisfy the morphological or immunophenotypical criteria for any of the above categories. These processes are best left unclassified. © 1993 Baillière Tindall. All rights reserved.

引用

页码：767 / 783

页数：17

共 45 条

[1]

[Anonymous], 1989, Ann Intern Med, V110, P236

[2] LEUKEMIA AS A MANIFESTATION OF LARGE CELL LYMPHOMA [J].