Ott G, Kalla J, Steinhoff A, Rosenwald A, Katzenberger T, Roblick U, Ott M M, Müller-Hermelink H K
Institute for Pathology, University of Würzburg, Germany.
Am J Pathol. 1998 Sep;153(3):689-94. doi: 10.1016/S0002-9440(10)65611-8.
The genetic background of extranodal marginal zone B-cell non-Hodgkin's lymphoma (NHL) of mucosa-associated lymphoid tissue (MALT) type is poorly understood. In contrast to most entities of primary nodal lymphomas, few cytogenetic data are available, and gene rearrangements frequently encountered in and highly characteristic of certain entities of systemic NHL are absent in this type of lymphoma. Recently, it was suggested that MALT-type NHLs are associated with certain numerical chromosome aberrations and especially with trisomy 3. We performed an extensive study using a sensitive double (bicolor) fluorescence in situ hybridization technique for the analysis of trisomies for chromosomes 3, 7, 12, and 18 in 60 samples of low-grade and 45 high-grade MALT-type tumors. In the low-grade cases, trisomy 3 was found in a frequency of only 20%. High-grade lymphomas of MALT type were associated with trisomies 3, 7, 12, and 18 in 36, 20, 18, and 13% of the cases, respectively. Whereas no difference was encountered for trisomy 3 in primary and secondary/simultaneous high-grade lymphomas, +7 and +12 were associated with primary lymphomas, and a +18 was predominantly found in secondary/simultaneous high-grade NHL. These results challenge earlier reports describing a high frequency of +3 in low-grade MALT-type NHL and indicate a possibly different genetic evolution pattern of primary and secondary/simultaneous high-grade lymphomas of primary mucosal origin.
黏膜相关淋巴组织(MALT)型结外边缘区B细胞非霍奇金淋巴瘤(NHL)的遗传背景目前了解甚少。与大多数原发性淋巴结淋巴瘤不同,有关细胞遗传学的数据很少,并且在这种类型的淋巴瘤中不存在某些全身性NHL实体中经常出现且具有高度特征性的基因重排。最近,有人提出MALT型NHL与某些染色体数目畸变有关,尤其是与3号染色体三体有关。我们进行了一项广泛的研究,使用灵敏的双色荧光原位杂交技术分析60例低级别和45例高级别MALT型肿瘤样本中的3、7、12和18号染色体三体情况。在低级别病例中,仅20%的样本发现有3号染色体三体。MALT型高级别淋巴瘤分别有36%、20%、18%和13%的病例与3、7、12和18号染色体三体有关。虽然原发性和继发性/同时性高级别淋巴瘤在3号染色体三体方面没有差异,但+7和+12与原发性淋巴瘤有关,而+18主要见于继发性/同时性高级别NHL。这些结果对早期关于低级别MALT型NHL中+3频率较高的报道提出了质疑,并表明原发性黏膜起源的原发性和继发性/同时性高级别淋巴瘤可能具有不同的遗传进化模式。