Tian Yike, Huang Ping, Jiang Mi, Wu Jing, Cai Wei
The First Clinical College of Chongqing Medical University, No.1, Youyi Road, Yuzhong District, Chongqing, 400042, China.
Department of Laboratory Medicine, Fengdu County Hospital of Traditional Chinese Medicine, No.98, East Section of Pingdu Avenue, Fengdu County, Chongqing, 408200, China.
Discov Oncol. 2025 Aug 26;16(1):1629. doi: 10.1007/s12672-025-03449-4.
Acute lymphoblastic leukemia (ALL) is a malignant disease characterized by the clonal proliferation of precursor lymphoblasts in the bone marrow. Granular acute lymphoblastic leukemia (G-ALL) is a rare subtype of ALL, primarily associated with B-cell lineage. Traditionally, cytoplasmic granules indicate myeloid leukemia cell differentiation, as primitive lymphoblasts typically lack cytoplasmic granules. Therefore, the immature lymphoblasts in G-ALL may be mistaken for granular myeloid progenitor cells, causing potential diagnostic errors. The involvement of the BCOR gene in acute lymphoblastic leukemia has not been well-documented. This study examines the clinical data of a G-ALL patient, reviews relevant literature, and aims to improve disease recognition among clinicians and laboratory personnel, enhance diagnostic accuracy, and reduce instances of misdiagnosis and mistreatment.
急性淋巴细胞白血病(ALL)是一种恶性疾病,其特征为骨髓中前体淋巴细胞的克隆性增殖。颗粒性急性淋巴细胞白血病(G-ALL)是ALL的一种罕见亚型,主要与B细胞谱系相关。传统上,细胞质颗粒表明髓系白血病细胞分化,因为原始淋巴细胞通常缺乏细胞质颗粒。因此,G-ALL中未成熟的淋巴细胞可能会被误认为是颗粒性髓系祖细胞,从而导致潜在的诊断错误。BCOR基因在急性淋巴细胞白血病中的作用尚未得到充分记录。本研究检查了一名G-ALL患者的临床数据,回顾了相关文献,旨在提高临床医生和实验室人员对该疾病的认识,提高诊断准确性,减少误诊和误治情况。