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非霍奇金淋巴瘤的组织学亚型之间存在细胞遗传学异常差异。

There are differences in cytogenetic abnormalities among histologic subtypes of the non-Hodgkin's lymphomas.

作者信息

Levine E G, Arthur D C, Frizzera G, Peterson B A, Hurd D D, Bloomfield C D

出版信息

Blood. 1985 Dec;66(6):1414-22.

PMID:4063528
Abstract

Although many recurring chromosome abnormalities have been found in malignant lymphoma (ML) in recent years, their relationship to histology remains largely undefined. We have correlated, in the same tumor mass, chromosome findings with histology, defined by the International Working Formulation for Clinical Usage, in 120 patients. We find differences among histologies in the frequency of normal metaphases and the modal number of the predominant abnormal clone. In addition, most histologies have been significantly (P less than .01) associated with specific chromosome abnormalities. In particular, ML, follicular, predominantly small cleaved cell was associated with t(14;18)(q32;q21); ML, follicular, mixed small cleaved cell and large cell with t(14;18)(q32;q21) and trisomy 8; ML, follicular, predominantly large cell with trisomy 7 and breaks in 17q21-q25; ML, diffuse, mixed small cell and large cell with breaks in 11p; ML, diffuse, large cell with trisomy 21 and breaks in 2q and 9q; ML, large cell, immunoblastic with breaks at 6q21; and ML, small noncleaved cell with t(8;14)(q24;q32). Only the associations with t(14;18) and t(8;14) have been previously reported. The associated chromosome abnormality usually occurred in 30% to 70% of a given histology, raising the possibility that cytogenetics may add important prognostic information in lymphoma as it does in the acute leukemias.

摘要

近年来,尽管在恶性淋巴瘤(ML)中发现了许多复发性染色体异常,但其与组织学的关系在很大程度上仍不明确。我们对120例患者同一肿瘤块中的染色体检查结果与组织学进行了相关性分析,组织学依据国际临床应用工作分类法进行定义。我们发现,不同组织学类型在正常中期相频率和主要异常克隆的众数上存在差异。此外,大多数组织学类型与特定的染色体异常显著相关(P<0.01)。具体而言,滤泡性ML,主要为小裂细胞型与t(14;18)(q32;q21)相关;滤泡性ML,混合小裂细胞和大细胞型与t(14;18)(q32;q21)及8号染色体三体相关;滤泡性ML,主要为大细胞型与7号染色体三体及17q21-q25断裂相关;弥漫性ML,混合小细胞和大细胞型与11p断裂相关;弥漫性ML,大细胞型与21号染色体三体及2q和9q断裂相关;大细胞型ML,免疫母细胞型与6q21断裂相关;小无裂细胞型ML与t(8;14)(q24;q32)相关。只有与t(14;18)和t(8;14)的相关性此前有过报道。特定组织学类型中,相关染色体异常通常出现在30%至70%的病例中,这增加了细胞遗传学可能像在急性白血病中一样为淋巴瘤提供重要预后信息的可能性。

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There are differences in cytogenetic abnormalities among histologic subtypes of the non-Hodgkin's lymphomas.非霍奇金淋巴瘤的组织学亚型之间存在细胞遗传学异常差异。
Blood. 1985 Dec;66(6):1414-22.
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引用本文的文献

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The detection of t(14;18) in archival lymph nodes: development of a fluorescence in situ hybridization (FISH)-based method and evaluation by comparison with polymerase chain reaction.存档淋巴结中t(14;18)的检测:基于荧光原位杂交(FISH)方法的开发及与聚合酶链反应比较的评估
J Mol Diagn. 2003 Aug;5(3):168-75. doi: 10.1016/S1525-1578(10)60469-2.
2
Trisomy 3 is not a common feature in malignant lymphomas of mucosa-associated lymphoid tissue type.3号染色体三体并非黏膜相关淋巴组织型恶性淋巴瘤的常见特征。
Am J Pathol. 1998 Sep;153(3):689-94. doi: 10.1016/S0002-9440(10)65611-8.
3
Molecular characterization of primary mediastinal B cell lymphoma.
原发性纵隔B细胞淋巴瘤的分子特征
Am J Pathol. 1996 Jun;148(6):2017-25.
4
bcl-2 gene rearrangement analysis of Japanese follicular lymphomas by polymerase chain reaction in formalin-fixed, paraffin-embedded tissue specimens.通过聚合酶链反应对福尔马林固定、石蜡包埋组织标本中的日本滤泡性淋巴瘤进行bcl-2基因重排分析。
Jpn J Cancer Res. 1993 Jan;84(1):37-41. doi: 10.1111/j.1349-7006.1993.tb02781.x.
5
High expression of bcl-2 is the rule in acute lymphoblastic leukemia, except in Burkitt subtype at presentation, and is not correlated with the prognosis.bcl-2的高表达在急性淋巴细胞白血病中很常见,但初诊时的伯基特亚型除外,且与预后无关。
Ann Hematol. 1994 Jul;69(1):17-24. doi: 10.1007/BF01757343.
6
Rearrangement of bcl-2 is detectable in Hodgkin's disease by polymerase chain reaction.通过聚合酶链反应可在霍奇金病中检测到bcl - 2重排。
Jpn J Cancer Res. 1994 Dec;85(12):1229-32. doi: 10.1111/j.1349-7006.1994.tb02934.x.
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Localization of a lymphocyte-specific protein tyrosine kinase gene (lck) at a site of frequent chromosomal abnormalities in human lymphomas.淋巴细胞特异性蛋白酪氨酸激酶基因(lck)在人类淋巴瘤常见染色体异常位点的定位。
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