混合表型急性白血病伴低二倍体儿科患者

Elizabeth G. Salazar, G. Wertheim, J. Biegel, W. Hwang, S. Tasian, S. Rheingold
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引用次数: 3

摘要

我们描述了一个16岁的女性混合表型急性白血病B/髓系,NOS(以前的双表型白血病)与隐藏的次二倍体和体细胞TP53和CDKN2A/B缺失的病例。她通过淋巴细胞导向的多药化疗获得了形态缓解,但在最初诊断后11个月出现了早期髓质复发。她的病例详细介绍了一名谱系不明确的白血病患者的低二倍体的不寻常发现,并强调了这些高风险患者治疗选择的复杂性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mixed Phenotype Acute Leukemia with Low Hypodiploidy in a Pediatric Patient
We describe the case of a 16 year-old female with mixed phenotype acute leukemia B/myeloid, NOS (formerly biphenotypic leukemia) with masked hypodiploidy and somatic TP53 and CDKN2A/B deletions. She achieved morphologic remission with lymphoid-directed multi-agent chemotherapy, but experienced an early medullary relapse 11 months from initial diagnosis. Her case details the unusual finding of hypodiploidy in a patient with ambiguous lineage leukemia and highlights the complexity of therapy selection for these high-risk patients.
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