Torii Yuka, Nanjo Kana, Toubai Tomomi, Hosokawa Masashi, Sato Ryo, Yamada Akane, Aizawa Keiko, Himuro Masahito, Ito Satoshi, Yamamoto Masakazu, Magenau John, Wilcox Ryan, Ishizawa Kenichi
Department of Internal Medicine III, Division of Hematology and Cell Therapy, Yamagata University faculty of Medicine, 2-2-2 Iida-Nishi, Yamagata, 990-9585, Japan.
Faculty of Medicine, Yamagata University, Yamagata, Japan.
J Med Case Rep. 2021 May 25;15(1):285. doi: 10.1186/s13256-021-02885-4.
Chronic myeloid leukemia is a hematologic malignancy associated with the fusion of two genes: BCR and ABL1. This fusion results from a translocation between chromosomes 9 and 22, which is called the Philadelphia chromosome. Although the Philadelphia chromosome is present in more than 90% of patients with chronic myeloid leukemia, 5-8% of patients with chronic myeloid leukemia show complex variant translocations. Herein, we report a unique case of a three-way translocation variant in chronic phase chronic myeloid leukemia.
A 40-year-old Asian male who presented with leukocytosis was diagnosed with chronic phase chronic myeloid leukemia. Cytogenetic karyotyping analysis showed 46,XY,t(4;9;22)(q21;q34;q11.2). He was treated with bosutinib and then changed to dasatinib because of intolerance, and MR4.5 (BCR-ABL/ABL ≦ 0.0032%, international scale) was achieved after 17 months of continuous treatment.
This was the 14th case of t(4;9;22), in particular, a new variant Ph translocation involved in chromosome 4q21 and the first successful case treated with tyrosine kinase inhibitors in the world. We summarize previous case reports regarding three-way variant chromosome translocation, t(4;9;22) and discuss how this rare translocation is linked to prognosis.
慢性髓性白血病是一种与两个基因融合相关的血液系统恶性肿瘤:BCR和ABL1。这种融合是由9号和22号染色体之间的易位导致的,这被称为费城染色体。尽管超过90%的慢性髓性白血病患者存在费城染色体,但5-8%的慢性髓性白血病患者表现出复杂的变异易位。在此,我们报告一例慢性期慢性髓性白血病中三向易位变异的独特病例。
一名40岁的亚洲男性因白细胞增多症就诊,被诊断为慢性期慢性髓性白血病。细胞遗传学核型分析显示为46,XY,t(4;9;22)(q21;q34;q11.2)。他接受了博舒替尼治疗,后因不耐受改为达沙替尼治疗,持续治疗17个月后达到了MR4.5(BCR-ABL/ABL≤0.0032%,国际标准)。
这是第14例t(4;9;22)病例,特别是涉及4号染色体q21的一种新的变异型费城染色体易位,也是世界上首例用酪氨酸激酶抑制剂治疗成功的病例。我们总结了以往关于三向变异染色体易位t(4;9;22)的病例报告,并讨论了这种罕见易位与预后的关系。