造血细胞:急性淋巴细胞白血病的最高模仿者和细胞形态混淆者。

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL
Kanwaljeet Singh, Dwarika Tiwari, Revanth Boddu, Venkatesan Somasundarum, Kundan Mishra
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引用次数: 1

摘要

目的b淋巴细胞祖细胞,即造血细胞(HGs),不仅在诊断过程中,而且在化疗后评估骨髓缓解状态时,都可能给骨髓形态学评估带来问题。在这里,我们描述了一系列的12例急性淋巴细胞白血病(ALL),包括B-ALL和T-ALL病例,对缓解状态进行了评估,并在骨髓中发现了6 - 26%的母细胞样单核细胞,免疫表型分析表明是HGs。材料和方法本研究是在新德里陆军医院(转诊和研究)接受治疗的12例ALL病例的病例系列。所有病例均接受诱导后状态检查(第28天),并检查疑似All复发。进行骨髓抽吸(BMA)、活检和免疫分型。使用CD10、CD20、CD22、CD34、CD19和CD38抗体进行多色流式细胞术。结果12例BMA检查显示囊胚样细胞最高26%,最低6%,提示血液学复发的可能性。然而,在临床评估中,这些患者保存完好,外周血计数保存完好。因此,如上所述,骨髓抽吸物使用CD标记面板进行流式细胞术,显示hg。这些病例随后进行了微小残留病(MRD)分析,显示MRD阴性,进一步证实了我们的发现。结论本病例系列强调形态学和骨髓免疫分型在揭示诱导后ALL患者诊断困境中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Hematogones: The Supreme Mimicker and a Cytomorphological Confounder in Acute Lymphoblastic Leukemia.

Hematogones: The Supreme Mimicker and a Cytomorphological Confounder in Acute Lymphoblastic Leukemia.

Hematogones: The Supreme Mimicker and a Cytomorphological Confounder in Acute Lymphoblastic Leukemia.

Hematogones: The Supreme Mimicker and a Cytomorphological Confounder in Acute Lymphoblastic Leukemia.

Objective  B-lymphocyte progenitors, namely the hematogones (HGs), may pose problems in morphological assessment of bone marrow, not only during the diagnostic workup but also while evaluating bone marrow for remission status following chemotherapy. Here, we describe a series of 12 cases of acute lymphoblastic leukemia (ALL) that included both B-ALL and T-ALL cases, which were evaluated for remission status and revealed blast-like mononuclear cells in bone marrow in the range of 6 to 26%, which on immunophenotypic analysis turned out to be HGs. Materials and Methods  This is a case series of 12 ALL cases who were undergoing treatment at the Army Hospital (Referral and Research), New Delhi. All these cases were under workup for post-induction status (day 28) and to check for suspected ALL relapse. Bone marrow aspirate (BMA), biopsy, and immunophenotyping were performed. Multicolored flow cytometry was performed using CD10, CD20, CD22, CD34, CD19, and CD38 antibodies panel. Results  BMA assessment of 12 cases revealed a maximum of 26% blastoid cells and a minimum of up to 6%, raising the suspicion of hematological relapse. However, on clinical assessment, these patients were well preserved, with preserved peripheral counts. Hence, marrow aspirates were subjected to flow cytometry using the CD markers panel, as discussed above, which revealed HGs. These cases were followed by minimal residual disease (MRD) analysis that revealed MRD-negative status, further confirming our findings. Conclusion  This case series highlights the importance of morphology and bone marrow immunophenotyping in unveiling the diagnostic dilemma in post-induction ALL patients.

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来源期刊
Journal of Laboratory Physicians
Journal of Laboratory Physicians MEDICINE, GENERAL & INTERNAL-
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审稿时长
31 weeks
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