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淋巴母细胞淋巴瘤

Lymphoblastic lymphoma.

作者信息

Cortelazzo Sergio, Ferreri Andrés, Hoelzer Dieter, Ponzoni Maurilio

机构信息

Oncology Unit, Humanitas/Gavazzeni, Bergamo, Italy.

San Raffaele Scientific Institute, Milan, Italy.

出版信息

Crit Rev Oncol Hematol. 2017 May;113:304-317. doi: 10.1016/j.critrevonc.2017.03.020. Epub 2017 Mar 18.

Abstract

Lymphoblastic lymphoma (LBL) is a neoplasm of immature B cells committed to the B-(B-LBL) or T-cell lineage (T-LBL) that accounts for approximately 2% of all lymphomas. Although histological features are usually sufficient to distinguish lymphoblastic from mature B- or T-cell neoplasms, of greater importance for diagnosis is the characterization of immunophenotype by flow cytometry. LBL occurs more commonly in children than in adults, mostly in males. A bone marrow involvement <25% (or 20% according to WHO) formally distinguishes LBL from ALL. The prognosis of LBL has dramatically improved with the use of intensive ALL-type chemotherapy regimens, which includes intensive intrathecal chemotherapy prophylaxis and consolidation with mediastinal irradiation. Patients with adverse prognostic features assessed by postinduction CT/positron emission tomography scans (PET) and minimal residual disease analysis (MRD) should be considered for high-dose chemotherapy and stem cell transplantation. Further therapeutic progresses are expected from the introduction of new drugs and targeting agents.

摘要

淋巴母细胞淋巴瘤(LBL)是一种起源于未成熟B细胞且定向于B细胞系(B-LBL)或T细胞系(T-LBL)的肿瘤,约占所有淋巴瘤的2%。尽管组织学特征通常足以将淋巴母细胞性肿瘤与成熟B或T细胞肿瘤区分开来,但对于诊断更为重要的是通过流式细胞术对免疫表型进行特征描述。LBL在儿童中比在成人中更常见,且大多发生于男性。骨髓受累程度<25%(或根据世界卫生组织标准为20%)可将LBL与急性淋巴细胞白血病(ALL)正式区分开来。使用强化的ALL型化疗方案后,LBL的预后有了显著改善,这些方案包括强化鞘内化疗预防以及纵隔放疗巩固治疗。对于诱导后CT/正电子发射断层扫描(PET)和微小残留病分析(MRD)评估具有不良预后特征的患者,应考虑进行大剂量化疗和干细胞移植。新药和靶向药物的引入有望带来进一步的治疗进展。

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