Diagnosis of high risk lymphoma by molecular genotypic analysis: Bigenotype and multiple rearranged bands as risk factor.

N. Kimura, Takahisa Yoshida, M. Kikuchi
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Abstract

We examined 132 non-Hodgkin's lymphomas for rearrangements of TcR β and Ig genes. These histologic subclassification was based on the modified International Working Formulation (WF). Of these, 58 were derived from T-cell and 74 were from B-cell due to the results of immunophenotype. In high grade group of T-cell lymphomas, bigenotypic pattern with Cβ and JH probe was 14% and multiple rearranged bands pattern was 13%. On B-cell lymphomas, the bigenotypic pattern was 12% in high grade, 4.7% in intermediate grade and nothing in low grade. The multiband pattern was observed in only two cases (one is lymphoblastic subtype and the other one large). However, there is no corellation between the frequency of biphenotypic or multibands pattern, and WF subclassification in B-cell lymphoma. The presence of these specific rearrangement patterns in T-cell lymphoma (except for AILD) was associated with a poor prognosis. These findings indicate that the presence of bigenotypic and/or multibands pattern indentifies a high-risk group of patients with T-cell lymphoma.
分子基因型分析诊断高危淋巴瘤:双型和多重重排带是危险因素。
我们检测了132例非霍奇金淋巴瘤中TcR β和Ig基因的重排。这些组织学亚分类是基于改进的国际工作公式(WF)。其中58例来自t细胞,74例来自b细胞。在高级别t细胞淋巴瘤中,Cβ和JH探针双型型占14%,多重排带型占13%。在b细胞淋巴瘤中,重度双型占12%,中度为4.7%,低度为零。仅2例(1例为淋巴母细胞亚型,1例为大细胞亚型)可见多带型。然而,在b细胞淋巴瘤中,双表型或多波段模式的频率与WF亚分类之间没有相关性。这些特异性重排模式在t细胞淋巴瘤(AILD除外)中的存在与不良预后相关。这些发现表明,双型和/或多波段模式的存在确定了t细胞淋巴瘤患者的高风险群体。
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