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[大细胞间变性淋巴瘤:一项遗传学和免疫表型研究]

[Large-cell anaplastic lymphomas: a genetic and immunophenotypic study].

作者信息

Martínez B, Gonzalo I, Robledo M, Benítez J, Ageitos A, Marcos B, Echezarreta G, Sanz C, Rivas C

机构信息

Dpto. de Genética, Fundación Jiménez Díaz, Facultad de Medicina, Universidad Autónoma de Madrid.

出版信息

Sangre (Barc). 1995 Aug;40(4):293-9.

PMID:7482118
Abstract

PURPOSE

To characterize from a genetic point of view a group of non-Hodgkin's anaplastic large-cell lymphomas (ALCL) by Southern blot and PCR methods with different probes (molecular study) and with direct or post 24-78 hours cultures with GTC banding techniques (cytogenetic). To correlate the results to the immunophenotype performed with a complete panel of monoclonal antibodies (MoAb) according to avidin-biotine and alkaline phosphatase (APAAP) methods.

MATERIAL AND METHODS

Sixty cases of ALCL were reviewed and only 19 selected (with frozen or fresh material) because a complete immunohistologic and genotypic correlation had been done. According to CD15 expression two groups were considered, CD15+ (the so-called Hodgkin's related or Hodgkin's like) and CD15- or classical type.

RESULTS

Only 26.5% of cases showed immuno -genotypic correlation. Immunohistochemistry is an accurate method for activation, proliferation and B-cell nature, but T-cell cases were not stained because T-cell paraffin markers are not completely specific. CD15 group had only 30% rearranged cases with scarce cytogenetic abnormalities, as it occurs in Hodgkin's disease (HD). ALCL classical type showed 66% rearranged cases, and one of the T-cell cases showed an incomplete t (2:5) translocation or polyploid cell lines.

CONCLUSIONS

Both groups have different genetic and immunophenotypic behaviour which resembles HD or NHL. CD15 positive cases or ALCL HD-related constitute a borderline entity which has to be recognized because of the different therapy and clinical behaviour.

摘要

目的

通过Southern印迹法和聚合酶链反应(PCR)方法,使用不同探针(分子研究)以及采用GTC显带技术对直接培养或培养24 - 78小时后的样本进行分析(细胞遗传学),从遗传学角度对一组非霍奇金间变性大细胞淋巴瘤(ALCL)进行特征描述。将结果与根据抗生物素蛋白 - 生物素和碱性磷酸酶(APAAP)方法使用全套单克隆抗体(MoAb)进行的免疫表型分析结果相关联。

材料与方法

回顾了60例ALCL病例,仅选择了19例(有冷冻或新鲜样本),因为已进行了完整的免疫组织学和基因分型相关性研究。根据CD15表达情况分为两组,CD15 +(所谓的霍奇金相关或霍奇金样)和CD15 - 或经典型。

结果

仅26.5%的病例显示免疫 - 基因分型相关性。免疫组织化学是用于确定激活、增殖和B细胞性质的准确方法,但T细胞病例未被染色,因为T细胞石蜡标记物并非完全特异性。CD15组仅有30%的病例发生重排,细胞遗传学异常较少,这与霍奇金病(HD)的情况相同。ALCL经典型显示66%的病例发生重排,其中1例T细胞病例显示不完全的t(2;5)易位或多倍体细胞系。

结论

两组具有不同的遗传和免疫表型行为,类似于HD或NHL。CD15阳性病例或与HD相关的ALCL构成一个临界实体,因其治疗和临床行为不同而必须予以识别。

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