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在从骨髓增生异常综合征进展而来的急性髓性白血病中出现伴有p190 BCR/ABL嵌合转录本的费城染色体较晚。

Late appearance of Philadelphia chromosome with the p190 BCR/ABL chimeric transcript in acute myelogenous leukemia progressing from myelodysplastic syndrome.

作者信息

Kakihana Kazuhiko, Mizuchi Daisuke, Yamaguchi Mitsuko, Sakashita Chizuko, Fukuda Tetsuya, Yamamoto Koh, Miki Tohru, Murakami Naomi, Miura Osamu

机构信息

Department of Hematology and Oncology, Tokyo Medical and Dental University.

出版信息

Rinsho Ketsueki. 2003 Apr;44(4):242-8.

PMID:12784657
Abstract

We report a late appearance of the Philadelphia chromosome (Ph) with the p190 BCR/ABL chimeric transcript in a 69-year-old patient with acute myelogenous leukemia (AML) that had evolved from myelodysplastic syndrome (MDS). In July 1997, the patient was found to have pancytopenia caused by refractory anemia with excess of blasts, which evolved into AML in 4 months. The leukemic cells were positive for CD13, CD14, CD33, and HLA-DR and had a normal karyotype. The patient achieved a complete remission after combination chemotherapy. However, his leukemia relapsed in November 1999, with the appearance of leukemic cells positive for CD7, CD13, CD34, and HLA-DR with a 46, XY, add (18) (p11) karyotype. The patient failed to achieve the second remission after several courses of intensive chemotherapy. When the number of blastic cells, showing the same surface phenotypes, in the peripheral blood increased drastically in April 2000, chromosomal analysis of leukemic cells revealed a 46, XY, t(9;22) (q34;q11), add(18)(p11) karyotype. The fusion of the BCR and ABL genes was confirmed by fluorescence in situ hybridization analysis, and the reverse transcription-polymerase chain reaction analysis further revealed the presence of the p190 BCR/ABL chimeric transcript. The appearance of the Ph chromosome in the course of MDS transforming to AML is very rare and may be correlated to the disease progression.

摘要

我们报告了一名69岁急性髓系白血病(AML)患者出现费城染色体(Ph)及p190 BCR/ABL嵌合转录本较晚的情况,该患者由骨髓增生异常综合征(MDS)演变而来。1997年7月,患者因伴有过多原始细胞的难治性贫血导致全血细胞减少,4个月后演变为AML。白血病细胞CD13、CD14、CD33和HLA-DR呈阳性,核型正常。患者经联合化疗后达到完全缓解。然而,他的白血病于1999年11月复发,出现CD7、CD13、CD34和HLA-DR呈阳性的白血病细胞,核型为46, XY, add(18)(p11)。经过几个疗程的强化化疗,患者未能达到第二次缓解。2000年4月,外周血中具有相同表面表型的原始细胞数量急剧增加,白血病细胞的染色体分析显示核型为46, XY, t(9;22)(q34;q11), add(18)(p11)。通过荧光原位杂交分析证实了BCR和ABL基因的融合,逆转录-聚合酶链反应分析进一步显示存在p190 BCR/ABL嵌合转录本。在MDS转化为AML过程中出现Ph染色体非常罕见,可能与疾病进展相关。

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Late appearance of Philadelphia chromosome with the p190 BCR/ABL chimeric transcript in acute myelogenous leukemia progressing from myelodysplastic syndrome.在从骨髓增生异常综合征进展而来的急性髓性白血病中出现伴有p190 BCR/ABL嵌合转录本的费城染色体较晚。
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引用本文的文献

1
Philadelphia Translocation in MDS: A Case Report and a Brief Review of the Literature Looking at Its Prevalence, Disease Progression, and Treatment Options.骨髓增生异常综合征中的费城染色体易位:一例报告及对其患病率、疾病进展和治疗选择的文献简要综述
Case Rep Hematol. 2018 Nov 22;2018:5865321. doi: 10.1155/2018/5865321. eCollection 2018.
2
Cryptic e1a2 BCR-ABL1 fusion with complex chromosomal abnormality in de novo myelodysplastic syndrome.初发骨髓增生异常综合征中具有复杂染色体异常的隐匿性e1a2 BCR-ABL1融合
Ann Lab Med. 2015 Nov;35(6):643-6. doi: 10.3343/alm.2015.35.6.643.