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首页> 外文期刊>Pediatrics international : >Persistent clonal chromosomal abnormalities in a chronic myeloid leukemia patient
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Persistent clonal chromosomal abnormalities in a chronic myeloid leukemia patient

机译:慢性粒细胞白血病患者的持续性克隆染色体异常

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摘要

Clonal cytogenetic abnormalities (CCA) in Philadelphia chromosome (Ph)-negative cells have been reported in a small population of adult chronic myelogenous leukemia (CML) patients during the clinical course, but CCA in pediatric CML patients are rarely reported. We herein report the case of an 8-year-old boy from the onset of CML. Although he had relapse after unrelated bone marrow transplantation when 9years old, he has since been in complete molecular response on imatinib mesylate treatment. Surprisingly, various CCA have been observed in this patient, including several reciprocal chromosomal translocations in Ph-negative cells for >12years. Although dysplasia in the bone marrow cells was identified, no overt transformation to myelodysplastic syndrome or acute myeloid leukemia has been observed. The cause of the CCA remains unknown in this patient, and careful observation is required.
机译:在临床过程中,少数成年慢性骨髓性白血病(CML)患者中已报告了费城染色体(Ph)阴性细胞的克隆细胞遗传学异常(CCA),但很少报道小儿CML患者的CCA。我们在此报告了CML发作时一个8岁男孩的病例。尽管他在9岁时进行无关的骨​​髓移植后已复发,但此后他就一直接受甲磺酸伊马替尼的完全分子反应。令人惊讶的是,在该患者中观察到了各种CCA,包括Ph阴性细胞中12年以上的染色体相互易位。尽管已鉴定出骨髓细胞中的不典型增生,但未观察到明显的转化为骨髓增生异常综合症或急性髓细胞性白血病。该患者的CCA病因尚不清楚,需要仔细观察。

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