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T-Lymphoblastic Leukemia/Lymphoma.

T淋巴母细胞白血病/淋巴瘤

You MJ,Medeiros LJ,Hsi ED

Abstract

To review important concepts from the 2013 Society for Hematopathology/European Association for Haematopathology Workshop session on T-acute lymphoblastic leukemia/T-lymphoblastic lymphoma (T-ALL/T-LBL).
Twenty-one submitted cases are reviewed and summarized, with emphasis on key diagnostic or biologic points, and supplemented with relevant literature citations.
Early T-cell precursor (ETP)-ALL represented about one-third of all cases submitted. It is important to recognize ETP-ALL, because these patients have a poor prognosis if treated with standard therapy. A consensus immunophenotype has been developed to aid in the recognition of these cases. Other cases submitted illustrated rare entities, including two cases of Philadelphia chromosome-positive T-ALL, two cases of T-ALL associated with MYC translocations, and single cases illustrating various diseases. A subset of cases submitted illustrated issues related to differential diagnosis of T-ALL/T-LBL.
In view of the growing importance of molecular genetic analysis in the diagnosis and prognosis of T-ALL/T-LBL, it is important for pathologists to keep abreast of these developments. Currently, routine histopathology, immunophenotyping, conventional cytogenetic analysis, fluorescence in situ hybridization, and clonality testing are usually adequate to establish the diagnosis. However, as therapies become more targeted, assessment for relevant genetic abnormalities, either through candidate gene or broad-scale unbiased approaches, may become necessary.

摘要

就2013血液病学会/欧洲血液病协会研讨会上关于T-急性淋巴母细胞性白血病/ T淋巴母细胞淋巴瘤(T-ALL/T-LBL)的重要概念进行了综述。

复习和总结了会上讨论的21个病例,重点是关键的诊断或分子生物学依据,并以引用的相关文献作为补充。

早期T细胞前体(ETP)-ALL约占所有提交病例的1/3。识别ETP-ALL是十分重要的,因为如果采用标准疗法治疗,这些患者的预后较差。已经提出了一个免疫表型共识帮助识别这样的病例。其他提交的病例展示了罕见的病变实体,包括2例费城染色体阳性T-ALL、2例MYC易位相关的T-ALL和1个表现为不同疾病的病例。提交的少部分病例说明了T-ALL/ T-LBL鉴别诊断相关问题。

鉴于T-ALL/T-LBL诊断和预后的分子遗传学检测重要性日益增加,病理学家紧跟这些发展是十分重要的。目前,常规组织病理学、免疫分型、常规细胞遗传学分析、荧光原位杂交和克隆性检测用于确定诊断通常是足够的。然而,由于治疗越来越具有靶向性,因此无论是通过候选基因、还是通过广谱无偏差方法,对相关遗传学异常进行评估可能是必要的。

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