A Novel Case of ABL2 Chromosomal Rearrangement in High-Risk B-Cell Acute Lymphoblastic Leukemia.

Yogita Rohil, Dhanlaxmi Shetty, Gaurav Narula, Shripad D Banavali
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Abstract

Objectives: Philadelphia chromosome-like acute lymphoblastic leukemia (Ph-like ALL) accounts for ~15% of patients with high-risk ALL with an activated tyrosine kinase profile similar to Philadelphia chromosome positive ALL, without the presence of BCR-ABL1 rearrangement. ABL-class genes (ABL1, ABL2, PDGFRB, CSF1R and CRLF2) comprise the second major subgroup of Ph-like ALL cases but presence of ABL2 gene rearrangement in leukemia is rarely reported. We report a novel case of ABL2 chromosomal rearrangement that results from t(1;7)(q25;q32) in a patient with high-risk ALL.

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高危b细胞急性淋巴母细胞白血病ABL2染色体重排的新病例。
目的:费城染色体样急性淋巴细胞白血病(Ph-like ALL)约占高风险ALL患者的15%,其酪氨酸激酶激活谱与费城染色体阳性ALL相似,但不存在BCR-ABL1重排。abl类基因(ABL1, ABL2, PDGFRB, CSF1R和CRLF2)是ph样ALL病例的第二大亚群,但ABL2基因重排在白血病中很少报道。我们报告了一例由t(1;7)(q25;q32)引起的高风险ALL患者ABL2染色体重排的新病例。
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