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[结内与结外弥漫性大B细胞淋巴瘤:临床病理特征、免疫表型及预后比较]

[Nodal versus extranodal diffuse large B-cell lymphoma: comparison of clinicopathologic features, immunophenotype and prognosis].

作者信息

Lu Jin-biao, Li Xiao-qiu, Zhang Pei-hong, Zhou Xiao-yan, Zhang Tai-ming, Li Xiao-mei, Zhu Xiong-zeng

机构信息

Department of Pathology, Cancer Hospital, Fudan University, Shanghai 200032, China.

出版信息

Zhonghua Bing Li Xue Za Zhi. 2007 Jul;36(7):470-3.

PMID:17845761
Abstract

OBJECTIVE

To study the clinicopathologic features and outcome of patients with diffuse large B-cell lymphoma (DLBCL), and to compare the differences between DLBCL of nodal and extranodal origins.

METHODS

One hundred and forty-two cases of de novo DLBCL collected during a 10-year period were reviewed. The clinicopathologic features and follow-up (2 - 108 months) data were analyzed. Tissue microarray blocks were performed and immunohistochemical studies using antibodies against CD10, bcl-6 and MUM1 were carried out. The cases were then further categorized into germinal center B cell-like (GCB) and non-GCB subtypes.

RESULTS

Primary gastrointestinal DLBCL often presented as early-stage disease (stage I or II) and was associated with low international prognostic index. They showed better prognosis than DLBCL of nodal and other extranodal origins. The positivity rates of CD10, bcl-6 and MUM1 were 19%, 51% and 58%, respectively. 36% of the cases belonged to GCB, while the remaining 64% were non-GCB. In general, DLBCL of extranodal origin showed more frequent bcl-6 expression than nodal DLBCL. As for extranodal DLBCL, GCB immunophenotype was often seen in thyroid and breast tumors, while testicular DLBCL usually carried a non-GCB immunophenotype.

CONCLUSIONS

DLBCL of various origins show a diversified GCB and non-GCB differentiation. Nodal and extranodal DLBCL, as well as extranodal DLBCL from different primary sites, carry different biologic characteristics and prognostic implications.

摘要

目的

研究弥漫性大B细胞淋巴瘤(DLBCL)患者的临床病理特征及预后,并比较淋巴结起源和结外起源的DLBCL之间的差异。

方法

回顾10年间收集的142例初发性DLBCL病例。分析其临床病理特征及随访(2 - 108个月)数据。制作组织芯片块,并使用抗CD10、bcl-6和MUM1抗体进行免疫组化研究。然后将病例进一步分为生发中心B细胞样(GCB)和非GCB亚型。

结果

原发性胃肠道DLBCL常表现为早期疾病(I期或II期),且国际预后指数较低。它们的预后比淋巴结起源和其他结外起源的DLBCL更好。CD10、bcl-6和MUM1的阳性率分别为19%、51%和58%。36%的病例属于GCB,其余64%为非GCB。一般来说,结外起源的DLBCL比淋巴结DLBCL更频繁地表达bcl-6。至于结外DLBCL,GCB免疫表型常见于甲状腺和乳腺肿瘤,而睾丸DLBCL通常具有非GCB免疫表型。

结论

不同起源的DLBCL表现出多样化的GCB和非GCB分化。淋巴结和结外DLBCL,以及来自不同原发部位的结外DLBCL,具有不同的生物学特征和预后意义。

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