...
首页> 外文期刊>Journal of pediatric hematology/oncology: Official journal of the American Society of Pediatric Hematology/Oncology >A boy with acute lymphoblastic leukemia acquired clonal and nonclonal cytogenetic abnormalities including del(7q) and del(20q) without clinical evidence of disease after sex-mismatched cord blood transplantation.
【24h】

A boy with acute lymphoblastic leukemia acquired clonal and nonclonal cytogenetic abnormalities including del(7q) and del(20q) without clinical evidence of disease after sex-mismatched cord blood transplantation.

机译:患有急性淋巴细胞白血病的男孩在性别不匹配的脐带血移植后获得了克隆和非克隆细胞遗传异常,包括del(7q)和del(20q),而没有临床证据表明该疾病。

获取原文
获取原文并翻译 | 示例

摘要

An 8-year-old boy was diagnosed with precursor B-cell acute lymphoblastic leukemia. After intensified chemotherapy, he underwent sex-mismatched allogeneic cord blood transplantation. Postcord blood transplantation cytogenetic studies revealed engraftment failure evidenced by switching into the recipient type (XY), and, notably, various complex chromosomal aberrations in the recipient cells. Nonclonal and clonal aberrations including deletions of 7q and 20q were persistently observed. Nonetheless, the patient was clinically stable without evidence of marrow dysplasia or leukemic cells. Del(7q) and del(20q), 2 recurrent chromosomal aberrations in myeloid neoplasia, might represent underlying genomic instability in this patient, not the direct culprits of dysplasia or leukemogenesis.
机译:一个8岁男孩被诊断​​患有前体B细胞急性淋巴细胞白血病。加强化疗后,他接受了性别不匹配的异基因脐带血移植。脐带血移植后的细胞遗传学研究显示,移植失败可通过转换为受体类型(XY)来证明,尤其是受体细胞中各种复杂的染色体畸变。持续观察到包括7q和20q缺失在内的非克隆和克隆畸变。尽管如此,该患者临床稳定,没有骨髓异常增生或白血病细胞的迹象。 Del(7q)和del(20q),髓样瘤形成中的2个复发性染色体畸变,可能代表该患者潜在的基因组不稳定,而不是发育异常或白血病发生的直接元凶。

著录项

相似文献

  • 外文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号