Venetoclax联合阿扎胞苷治疗与治疗相关的三龄混合表型急性白血病。

IF 1.1 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
Internal Medicine Pub Date : 2025-09-01 Epub Date: 2025-02-08 DOI:10.2169/internalmedicine.4898-24
Jotaro Yamamoto, Kyosuke Yamaguchi, Otoya Watanabe, Kosei Kageyama, Yuki Taya, Daisuke Kaji, Aya Nishida, Hironori Uruga, Shinsuke Takagi, Kazuya Ishiwata, Hisashi Yamamoto, Akiko Masuda, Yutaka Takazawa, Go Yamamoto, Yuki Mori, Naoyuki Uchida, Atsushi Wake
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引用次数: 0

摘要

这是第一个以b细胞、t细胞和骨髓谱系表型为特征的治疗相关混合表型急性白血病(MPAL)的报道。一名68岁的男性,在食管癌复发的放化疗后完全缓解,出现细菌性肺炎,外周血中原细胞增加,随后的骨髓活检显示85.2%的原细胞。流式细胞术分析显示cytMPO+、CD19+、cytCD22+和cytCD3+标记物。患者被诊断为治疗相关性MPAL (B/T/髓系)。在开始使用venetoclax和阿扎胞苷后,患者完全缓解,并进行脐带血移植。本病例为治疗相关的三岁期MPAL治疗提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Therapy-related Trilineage Mixed Phenotype Acute Leukemia Treated with Venetoclax and Azacitidine.

This is the first report of therapy-related mixed-phenotype acute leukemia (MPAL) characterized by B-cell, T-cell, and myeloid lineage phenotypes. A 68-year-old man, who was in complete remission after chemoradiotherapy for recurrent esophageal cancer, developed bacterial pneumonia with increasing blasts in the peripheral blood, and a subsequent bone marrow biopsy revealed 85.2% blasts. A flow cytometric analysis revealed cytMPO+, CD19+, cytCD22+, and cytCD3+ markers. The patient was diagnosed with therapy-related MPAL (B/T/myeloid lineage). After the initiation of venetoclax and azacitidine, the patient achieved complete remission, and cord blood transplantation was performed. This case provides novel insights into the therapeutic options for therapy-related trilineage MPAL treatment.

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来源期刊
Internal Medicine
Internal Medicine 医学-医学:内科
CiteScore
1.90
自引率
8.30%
发文量
0
审稿时长
2.2 months
期刊介绍: Internal Medicine is an open-access online only journal published monthly by the Japanese Society of Internal Medicine. Articles must be prepared in accordance with "The Uniform Requirements for Manuscripts Submitted to Biomedical Journals (see Annals of Internal Medicine 108: 258-265, 1988), must be contributed solely to the Internal Medicine, and become the property of the Japanese Society of Internal Medicine. Statements contained therein are the responsibility of the author(s). The Society reserves copyright and renewal on all published material and such material may not be reproduced in any form without the written permission of the Society.
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