Occurrence of the t(2;5)(p23;q35) in non-Hodgkin's lymphoma

被引:53
作者
Weisenburger, DD
Gordon, BG
Vose, JM
Bast, MA
Chan, WC
Greiner, TC
Anderson, JR
Sanger, WG
机构
[1] UNIV NEBRASKA, MED CTR, DEPT PEDIAT, OMAHA, NE 68198 USA
[2] UNIV NEBRASKA, MED CTR, DEPT INTERNAL MED, OMAHA, NE 68198 USA
[3] UNIV NEBRASKA, MED CTR, DEPT PREVENT & SOCIETAL MED, OMAHA, NE 68198 USA
关键词
D O I
10.1182/blood.V87.9.3860.bloodjournal8793860
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Primary CD30(Ki-1)-positive anaplastic large-cell lymphoma (ALCL) is considered by some to be a distinct clinicopathologic entity associated with the t(2;5) (p23;q35). However, the specificity of t(2;5) for ALCL has not been carefully studied. Therefore, we performed a detailed analysis of all cases of ALCL with abnormal cytogenetics results in the Nebraska Lymphoma Study Group registry, as well as all other cases of non-Hodgkin's lymphoma with t(2;5) in the registry. We found the t(2;5) in only five of 10 cases of ALCL, four of whom were young patients. However, we also found the t(2;5) in 11 other cases of nonanaplastic lymphoma, including eight children with typical peripheral T-cell lymphomas of various types. The t(2;5) was also found in three older adults with B-cell lymphomas of various types. Thus, the t(2;5) was not specific for CD30(+) ALCL. However, t(2;5) may define a clinicopathologic entity in children and young adults characterized by variable morphologies with a T-cell or indeterminate phenotype, CD30-positivity, nodal disease with frequent extranodal involvement, advanced stage, and an excellent response to therapy, including bone marrow transplantation for relapsed disease. The clinical relevance of the t(2;5) in older patients requires further study. (C) 1996 by The American Society of Hematology.
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页码:3860 / 3868
页数:9
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