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[浆膜腔积液中淋巴母细胞淋巴瘤/急性淋巴细胞白血病的细胞学分析]

[Cytological analysis of lymphoblastic lymphoma/acute lymphoblastic leukemia in serous effusion].

作者信息

Xiao L, Xu J J, Zhang D D, Wei N, Kou J N, Li S L, Li W C

机构信息

Department of Pathology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.

出版信息

Zhonghua Bing Li Xue Za Zhi. 2021 Jan 8;50(1):49-54. doi: 10.3760/cma.j.cn112151-20200415-00319.

Abstract

To study the diagnostic clues and significance in serous effusion cytology associated with lymphoblatic lymphoma/acute lymphoblastic leukemia (LBL/ALL). Forty-five serous effusion specimens with final diagnosis of LBL/ALL were collected from August 2011 to December 2019 at the First Affiliated Hospital of Zhengzhou University. All cases were reviewed for their clinical profiles, cytomorphologic features and ancillary studies. Cell blocks and immunocytochemistry were prepared in 22 cases; flow cytometric immunophenotyping was performed in three cases and gene rearrangement analysis (T-cell recepter, TCR and immunoglobulin, Ig) was performed in five cases. Among the 45 cases, there were 35 males and 10 females with male to female ratio of 3.5∶1.0. The median age was 15 years. Mediastinal mass was the initial presentation in 39 patients (86.7%) and high LDL level were observed in 34 patients (75.6%). Microscopically, the majority of the specimens (86.7%) were hypercellular. The smears demonstrated dispersed lymphoblasts that were predominantly small to intermediate in size with scanty basophilic cytoplasm and irregular or convoluted nuclei with fine chromatin condensation and inconspicuous nucleoli. Mitoses were frequently observed. Karyorrhexis and apoptosis were seen in all cases. By immunophenotyping, TdT was expressed in 19 cases (86.4%) and CD99 in 20 cases (90.9%). Ki-67 expression varied from 65% to 95%. Flow cytometry in three cases demonstrated positivity for TdT, CD2, CD3 and CD7. Monoclonal TCR gene rearrangement was found in 4 of 5 cases, and both monoclonal TCR and Igκ gene were found in 1 case. In LBL/ALL, primary diagnosis could be made basing on clinical features (younger male patients with a mediastinum mass) and cytomorphology (monotonous, small to medium sized lymphoid cells with prominent irregular nuclei, fine chromatin and frequent mitoses, karyorrhexis and apoptosis). If immunocytochemistry and other ancillary studies are performed, the accuracy and reliability of the results could be improved.

摘要

研究浆液性积液细胞学检查对淋巴母细胞淋巴瘤/急性淋巴细胞白血病(LBL/ALL)的诊断线索及意义。收集2011年8月至2019年12月郑州大学第一附属医院最终诊断为LBL/ALL的45例浆液性积液标本。对所有病例的临床资料、细胞形态学特征及辅助检查进行回顾性分析。22例制备细胞块并行免疫细胞化学检测;3例行流式细胞术免疫表型分析;5例行基因重排分析(T细胞受体,TCR和免疫球蛋白,Ig)。45例中,男性35例,女性10例,男女比例为3.5∶1.0。中位年龄为15岁。39例患者(86.7%)以纵隔肿块为首发表现,34例患者(75.6%)观察到高乳酸脱氢酶(LDH)水平。显微镜下,大多数标本(86.7%)细胞增多。涂片显示散在的淋巴母细胞,大多为小至中等大小,嗜碱性胞质稀少,核不规则或呈卷曲状,染色质细呈凝聚状,核仁不明显。常见有丝分裂。所有病例均可见核碎裂和凋亡。免疫表型分析显示,19例(86.4%)TdT阳性,20例(90.9%)CD99阳性。Ki-67表达率为65%至95%。3例流式细胞术检测显示TdT、CD2、CD3和CD7阳性。5例中有4例发现单克隆TCR基因重排,1例同时发现单克隆TCR和Igκ基因重排。对于LBL/ALL,可根据临床特征(年轻男性患者伴纵隔肿块)和细胞形态学(单一的、小至中等大小的淋巴细胞,核突出不规则,染色质细,常见有丝分裂、核碎裂和凋亡)做出初步诊断。若进行免疫细胞化学及其他辅助检查,可提高结果的准确性和可靠性。

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