涉及IGH和MALT1的t(14;18)(q32;q21)在皮肤黏膜相关淋巴组织淋巴瘤和原发性皮肤弥漫性大B细胞淋巴瘤中并不常见。

t(14;18)(q32;q21) involving IGH and MALT1 is uncommon in cutaneous MALT lymphomas and primary cutaneous diffuse large B-cell lymphomas.

作者信息

Wongchaowart Nicholas T, Kim Bong, Hsi Eric D, Swerdlow Steven H, Tubbs Raymond R, Cook James R

机构信息

Department of Clinical Pathology, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.

出版信息

J Cutan Pathol. 2006 Apr;33(4):286-92. doi: 10.1111/j.0303-6987.2006.00459.x.

Abstract

BACKGROUND

t(14;18)(q32;q21) involving IGH and MALT1 has been demonstrated in cutaneous MALT lymphomas and in one case of primary cutaneous diffuse large B-cell lymphoma (DLBCL). However, the incidence of IGH/MALT1 translocations in these forms of cutaneous lymphoma remains unclear.

METHODS

We performed paraffin section interphase fluorescence in situ hybridization (FISH) analysis using MALT1 and IGH break-apart probes on 16 cutaneous MALT lymphomas and 16 primary cutaneous DLBCL in order to assess the frequency of IGH/MALT1 translocations and to screen for other potential translocations involving the IGH or MALT1 loci.

RESULTS

Translocations involving MALT1 were not detected in any of 16 cutaneous MALT lymphomas or 16 primary cutaneous DLBCL. Of the 12 MALT lymphomas that could be analyzed for an IGH translocation, all were negative. In contrast, four of the 13 cases (31%) of primary cutaneous DLBCL that could be analyzed for translocations involving IGH were positive. Subsequent FISH analysis demonstrated one of these to be an IGH/BCL2 translocation and one to be a CMYC/IGH translocation, while the translocation partners in the remaining two cases are currently unidentified.

CONCLUSIONS

This study demonstrates that translocations involving MALT1, including IGH/MALT1, are uncommon in cutaneous MALT lymphomas and primary cutaneous DLBCL. Other translocations involving IGH also are not involved in the pathogenesis of at least most cutaneous MALT lymphomas. In contrast, primary cutaneous DLBCL may contain one of several IGH translocations in a minority of cases.

摘要

背景

在皮肤黏膜相关淋巴组织淋巴瘤(MALT淋巴瘤)以及1例原发性皮肤弥漫性大B细胞淋巴瘤(DLBCL)中已证实存在涉及免疫球蛋白重链基因(IGH)和黏膜相关淋巴组织淋巴瘤易位蛋白1(MALT1)的t(14;18)(q32;q21)。然而,这些类型的皮肤淋巴瘤中IGH/MALT1易位的发生率仍不清楚。

方法

我们使用MALT1和IGH断裂分离探针,对16例皮肤MALT淋巴瘤和16例原发性皮肤DLBCL进行石蜡切片间期荧光原位杂交(FISH)分析,以评估IGH/MALT1易位的频率,并筛查涉及IGH或MALT1基因座的其他潜在易位。

结果

在16例皮肤MALT淋巴瘤或16例原发性皮肤DLBCL中均未检测到涉及MALT1的易位。在12例可分析IGH易位的MALT淋巴瘤中,所有结果均为阴性。相比之下,在13例可分析涉及IGH易位的原发性皮肤DLBCL病例中,有4例(31%)呈阳性。随后的FISH分析显示,其中1例为IGH/BCL2易位,1例为CMYC/IGH易位,而其余2例的易位伙伴目前尚未明确。

结论

本研究表明,包括IGH/MALT1在内的涉及MALT1的易位在皮肤MALT淋巴瘤和原发性皮肤DLBCL中并不常见。至少在大多数皮肤MALT淋巴瘤的发病机制中,其他涉及IGH的易位也未参与。相比之下,少数原发性皮肤DLBCL病例可能包含几种IGH易位中的一种。

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