伊马替尼治疗后伴+8,I(17q)(q10)和der(22)t(9;22)的慢性髓系白血病引起的急性嗜碱性白血病。

IF 2.1 Q3 HEMATOLOGY Journal of Blood Medicine Pub Date : 2023-01-01 DOI:10.2147/JBM.S412837
Peng Shan, Hang Dong, Shilan Li
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摘要

急性嗜碱性白血病(Acute basophilic leukemia, ABL)是由慢性髓系白血病(chronic myeloid leukemia, CML)发展而来,伴有大量肥大细胞(肥大细胞),并伴有复杂的核型。在这里,我们报告一位81岁的男性,因ABL病史而入院。他于2018年1月被诊断为慢性粒细胞白血病(CML),并以每日400mg的剂量使用伊马替尼。随后,于2022年1月同时发现骨髓中MCs丰富的ABL转化,核型复杂,包括48、XY、8三体(+8)、同染色体17(q10) [i(17)(q10)]和衍生染色体22 t(9;22) [der(22)t(9;22)]。总之,本病例中MCs数量的增加提示它们可能在CML的预后中发挥重要作用,并引发复杂核型的发展。此外,这是伊马替尼治疗期间首次报道的MCs丰富的CML引起的ABL,并与48、XY、+8、i(17)(q10)和der(22)t(9;22)共存。需要进一步的研究来更好地描述这种罕见的疾病。
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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Acute Basophilic Leukemia Arising from Chronic Myeloid Leukemia with +8, I(17q)(q10) and der(22)t(9;22) After Imatinib Therapy.

Acute basophilic leukemia (ABL) arising from chronic myeloid leukemia (CML) with abundant mast cells (MCs), coexisting with a complex karyotype is rare. Here, we report an 81-year-old man admitted to our hospital with a history of ABL. He was diagnosed with CML in the chronic phase in January 2018, and Imatinib was used at a daily dose of 400mg. Then, transformation to ABL with abundant MCs in the bone marrow and complex karyotypes including 48,XY, trisomy 8 (+8), isochromosome 17(q10) [i(17)(q10)], and derivative chromosome 22 t(9;22) [der(22)t(9;22)] were discovered simultaneously in January 2022. In conclusion, the increased number of MCs in our case is a reminder that they might play an important role in the prognosis of CML and trigger the development of complex karyotypes. Moreover, this is the first case report of ABL arising from CML with abundant MCs, coexisting with 48,XY, +8, i(17)(q10), and der(22)t(9;22), during Imatinib treatment. Further studies are needed to better characterize this rare condition.

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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
94
审稿时长
16 weeks
期刊介绍: The Journal of Blood Medicine is an international, peer-reviewed, open access, online journal publishing laboratory, experimental and clinical aspects of all topics pertaining to blood based medicine including but not limited to: Transfusion Medicine (blood components, stem cell transplantation, apheresis, gene based therapeutics), Blood collection, Donor issues, Transmittable diseases, and Blood banking logistics, Immunohematology, Artificial and alternative blood based therapeutics, Hematology including disorders/pathology related to leukocytes/immunology, red cells, platelets and hemostasis, Biotechnology/nanotechnology of blood related medicine, Legal aspects of blood medicine, Historical perspectives. Original research, short reports, reviews, case reports and commentaries are invited.
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