Acute leukemia with KMT2A rearrangement: A master of disguise

IF 0.7 Q4 HEMATOLOGY
Sawyer J. Bawek , Eunice S. Wang , Steven D. Green
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引用次数: 0

Abstract

Mixed-phenotype acute leukemia (MPAL) is a rare form of leukemia with ambiguous lineage, and there are challenges in accurately diagnosing this entity according to formal criteria. Here we report a case which was initially diagnosed as “AML” based on atypical peripheral blood flow cytometry that was subsequently determined to be B-ALL with KMT2A rearrangement based on marrow results. Although KMT2A rearrangements represent a defining genetic abnormality for acute leukemia of ambiguous lineage, this case did not meet the criteria for MPAL based on WHO 2022 criteria. This case highlights the diagnostic challenges of MPAL and the potential limitations of the current classification. We discuss the most appropriate workup and management of these patients and identify areas for future study.

伴有 KMT2A 重排的急性白血病:伪装大师
混合表型急性白血病(MPAL)是一种罕见的白血病,其血统不明确,根据正式标准准确诊断这种实体存在挑战。我们在此报告了一个病例,该病例最初根据非典型外周血流式细胞术诊断为 "急性髓细胞白血病",后来根据骨髓结果确定为伴有KMT2A重排的B-ALL。虽然 KMT2A 基因重排是血缘不清急性白血病的一种决定性基因异常,但根据世界卫生组织 2022 年的标准,该病例并不符合 MPAL 的标准。本病例凸显了 MPAL 的诊断难题和当前分类的潜在局限性。我们讨论了这些患者最合适的检查和治疗方法,并确定了未来的研究领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Leukemia Research Reports
Leukemia Research Reports Medicine-Oncology
CiteScore
1.70
自引率
0.00%
发文量
70
审稿时长
23 weeks
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