The usefulness of a rapid PCR methodology to detect rearranged Ig heavy chain genes in lymphoproliferative disease in a diagnostic setting

被引:5
作者
Angulo, RI
Bennetts, BH
Benson, EM
Tschuchnigg, MS
Kamath, S
机构
[1] WESTMEAD HOSP,ICPMR,DEPT IMMUNOPATHOL,WESTMEAD,NSW 2145,AUSTRALIA
[2] DAVIES & PARTNERS PATHOL,RHODES,NSW,AUSTRALIA
关键词
polymerase chain reaction; B-cell lymphoproliferative disease; immunoglobulin gene; leukemia; lymphoma;
D O I
10.1080/00313029500169293
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Polymerase chain reaction (PCR) was used to amplify the DNA fragments of the framework 3 region (FR3) of the immunoglobulin heavy (IgH) chain genes, from the tissue of 66 patients with B-lymphoproliferative diseases and 74 patients with other malignant diseases, reactive or normal tissue. The assay performed with 77% sensitivity, 100% specificity and 89% efficacy. In addition, the PCR assay cost less than 25% of the cost of performing Southern blot analysis oi tumor DNA, which has been the test performed to date, and had a turn around time of 24 hrs rather than the 7-14 days required to obtain a result from Southern blot analysis. These results suggest that PCR analysis of B-cell lymphoproliferative disease is superior to Southern blot analysis, in the setting of a diagnostic laboratory.
引用
收藏
页码:352 / 357
页数:6
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