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胸腺癌性 MALT 淋巴瘤的染色体畸变特征。

Characterization of chromosomal aberrations in thymic MALT lymphoma.

机构信息

Department of Pathology, Graduate School of Medical Sciences, Nagoya City University, Nagoya, Japan.

出版信息

Pathol Int. 2012 Feb;62(2):93-8. doi: 10.1111/j.1440-1827.2011.02764.x. Epub 2012 Jan 13.

DOI:10.1111/j.1440-1827.2011.02764.x
PMID:22243778
Abstract

Mucosa-associated lymphoid tissue (MALT) lymphoma arising in the thymus is a rare disorder that shows a strong association with autoimmune disease. Several MALT-lymphoma-specific and -associated chromosomal abnormalities, including t(11;18), t(14;18), t(1;14), trisomy 3 and trisomy 18, are known to occur. The former translocation results in apoptosis inhibitor 2 gene (API2)-MALT lymphoma-associated translocation 1 (MALT1) fusion. In this study, we examined 14 cases of thymic MALT lymphomas for API2-MALT1 fusion using multiplex reverse transcription polymerase chain reaction and looked for trisomy 3, trisomy 18 and abnormalities of MALT1 and IGH genes using fluorescence in situ hybridization. Thymic MALT lymphoma cases had a high frequency of trisomy 3 (7/14 cases), a very low incidence of trisomy 18 (1/14) and no detectable MALT1-associated (0/13) or IGH-associated (0/13) gene abnormalities including t(11;18). A review of the literature showed that the pattern of chromosomal aberrations in thymic MALT lymphoma was similar to those of thyroid and salivary gland MALT lymphomas. Although frequently detected, trisomy 3 was not associated with any of the clinicopathological factors analyzed, suggesting that trisomy 3 may play a role in lymphoma development. In conclusion, the present study showed that thymic MALT lymphoma has a characteristic pattern of chromosomal aberrations that may be similar to those of other autoimmune-associated MALT lymphomas.

摘要

黏膜相关淋巴组织(MALT)淋巴瘤发生在胸腺是一种罕见的疾病,与自身免疫性疾病密切相关。已知几种 MALT 淋巴瘤特异性和相关性染色体异常,包括 t(11;18)、t(14;18)、t(1;14)、三体 3 和三体 18,前者易位导致凋亡抑制因子 2 基因(API2)-MALT 淋巴瘤相关易位 1(MALT1)融合。在这项研究中,我们使用多重反转录聚合酶链反应检查了 14 例胸腺 MALT 淋巴瘤的 API2-MALT1 融合,并使用荧光原位杂交检查了三体 3、三体 18 和 MALT1 和 IGH 基因的异常。胸腺 MALT 淋巴瘤病例三体 3 的频率很高(7/14 例),三体 18 的发生率非常低(1/14),未检测到 MALT1 相关(0/13)或 IGH 相关(0/13)基因异常,包括 t(11;18)。文献复习表明,胸腺 MALT 淋巴瘤的染色体畸变模式与甲状腺和唾液腺 MALT 淋巴瘤相似。尽管经常检测到,但三体 3与分析的任何临床病理因素均无关,提示三体 3可能在淋巴瘤的发生中起作用。总之,本研究表明胸腺 MALT 淋巴瘤具有特征性的染色体异常模式,可能与其他自身免疫相关的 MALT 淋巴瘤相似。

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