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CD19阴性B系急性淋巴细胞白血病:诊断与治疗挑战

CD19-negative B-lineage acute lymphoblastic leukemia: A diagnostic and therapeutic challenge.

作者信息

Bansal Shashi, Sharma Upendra, Jain Akansha, Sharma Richa, Yagnik Bhargav

机构信息

Department of Pathology, Bhagwan Mahaveer Cancer Hospital and Research Centre, Jaipur, Rajasthan, India.

Department of Clinical Hematology, Bhagwan Mahaveer Cancer Hospital and Research Centre, Jaipur, Rajasthan, India.

出版信息

Indian J Pathol Microbiol. 2017 Oct-Dec;60(4):596-598. doi: 10.4103/IJPM.IJPM_379_17.

Abstract

B-lineage acute lymphoblastic leukemia (B-ALL) is an aggressive neoplasm of B-lymphocyte precursors that express the pan B-cell marker CD19 in all the cases. Rarely, a case may be assigned as B-lineage even if CD19 is negative. Here, a 16-year-old male presented with complaints of pain abdomen, on and off fever, joint pain, and hepatosplenomegaly for 2 months. Bone marrow examination was suggestive of acute leukemia with numerous leukoblasts on aspiration. On flow cytometry, gated blast population was negative for CD19, cytoCD3, and myeloperoxidase MPO and positive for CD34, TdT, HLA-DR, CD22, CD79a, and CD10. Immunohistochemistry study showed positivity for TdT, CD34, CD10 (focal), and PAX 5 and negativity for CD20, CD3, MPO, CD117, and CD68. Lack of awareness of negative CD19 expression in B-ALL can lead to incorrect immunophenotypic diagnosis, treatment, and monitoring of B-ALL. Proper diagnosis should be based on clinical features, immunophenotypic profiles, immunohistochemistry findings, and molecular analysis.

摘要

B 系急性淋巴细胞白血病(B-ALL)是一种侵袭性的 B 淋巴细胞前体肿瘤,所有病例均表达泛 B 细胞标志物 CD19。极少数情况下,即使 CD19 呈阴性,病例也可能被归类为 B 系。在此,一名 16 岁男性因腹痛、间断发热、关节疼痛和肝脾肿大 2 个月前来就诊。骨髓检查提示为急性白血病,穿刺可见大量原始细胞。流式细胞术检测显示,门控原始细胞群 CD19、胞质 CD3 和髓过氧化物酶(MPO)呈阴性,而 CD34、末端脱氧核苷酸转移酶(TdT)、人类白细胞抗原-DR(HLA-DR)、CD22、CD79a 和 CD10 呈阳性。免疫组织化学研究显示 TdT、CD34、CD10(局灶性)和 PAX 5 呈阳性,而 CD20、CD3、MPO、CD117 和 CD68 呈阴性。对 B-ALL 中 CD19 表达阴性缺乏认识可能导致 B-ALL 的免疫表型诊断、治疗及监测出现错误。正确的诊断应基于临床特征、免疫表型谱、免疫组织化学结果及分子分析。

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