Kansal Rina, Sait Sheila N J, Block AnneMarie W, Ward Pamela M, Kelly Felicity L R, Cheney Richard T, Czuczman Myron, Brecher Martin L, Barcos Maurice
Department of Pathology, Buffalo General Hospital, The State University of New York, Buffalo, NY, USA.
Mod Pathol. 2005 Feb;18(2):235-43. doi: 10.1038/modpathol.3800299.
The purpose of this study was to evaluate fluorescence in situ hybridization abnormalities of the 2p23 anaplastic lymphoma kinase (ALK) gene loci in lymphomas with anaplastic morphology. We studied 24 anaplastic large cell lymphomas (ALCL) classified by World Health Organization criteria [17 primary nodal/systemic (10 ALK+, 7 ALK-), seven primary cutaneous], and 17 additional non-Hodgkin's lymphomas [one ALK+ B-lineage lymphoma, 14 ALK- diffuse large B-cell lymphomas (seven anaplastic variants, five nonanaplastic, two secondary CD30+), two follicular lymphomas]. ALK- lymphomas with anaplastic morphology showed extra nonrearranged anaplastic lymphoma kinase gene loci (P=0.004) due to trisomy 2 irrespective of the following factors: B or T/null phenotype (P=0.315), diagnostic categories of systemic or cutaneous ALCL or the above-mentioned B-cell lymphomas (P=0.131), and CD30 positivity by immunohistochemistry (P=1.000). Trisomy 2 was absent in all ALK+ lymphomas (P=0.009), which showed rearranged ALK gene loci (P<0.001). Whether trisomy 2 is a primary or secondary event that leads to ALK- lymphomas cannot be determined from this study. Its presence in secondary B-cell lymphomas suggests that trisomy 2 may be a secondary cytogenetic aberration in lymphomas in general. Further investigation of this finding is necessary to further our understanding of the heterogeneous group of ALK- lymphomas.
本研究的目的是评估具有间变性形态的淋巴瘤中2p23间变性淋巴瘤激酶(ALK)基因位点的荧光原位杂交异常情况。我们研究了24例根据世界卫生组织标准分类的间变性大细胞淋巴瘤(ALCL)[17例原发性淋巴结/系统性(10例ALK阳性,7例ALK阴性),7例原发性皮肤性],以及另外17例非霍奇金淋巴瘤[1例ALK阳性B细胞淋巴瘤,14例ALK阴性弥漫性大B细胞淋巴瘤(7例间变性变体,5例非间变性,2例继发性CD30阳性),2例滤泡性淋巴瘤]。具有间变性形态的ALK阴性淋巴瘤显示由于2号染色体三体导致额外的非重排间变性淋巴瘤激酶基因位点(P = 0.004),与以下因素无关:B或T/null表型(P = 0.315)、系统性或皮肤性ALCL或上述B细胞淋巴瘤的诊断类别(P = 0.131)以及免疫组织化学检测的CD30阳性(P = 1.000)。所有ALK阳性淋巴瘤均无2号染色体三体(P = 0.009),其显示ALK基因位点重排(P < 0.001)。本研究无法确定2号染色体三体是导致ALK阴性淋巴瘤的原发性还是继发性事件。其在继发性B细胞淋巴瘤中的存在表明2号染色体三体可能是一般淋巴瘤中的继发性细胞遗传学异常。有必要对这一发现进行进一步研究,以加深我们对ALK阴性淋巴瘤这一异质性群体的理解。