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[1;19易位的儿童急性淋巴细胞白血病的临床和细胞遗传学特征]

[Clinical and cytogenetic features in childhood acute lymphoblastic leukemia with 1; 19 translocation].

作者信息

Sikano T, Ishikawa Y, Konno M, Hatayama Y, Nakadate H, Hatae Y, Takeda T

机构信息

Department of Pediatrics of the Hokkaido University School of Medicine.

出版信息

Rinsho Ketsueki. 1990 Jun;31(6):793-8.

PMID:2214170
Abstract

We studied the clinical and cytogenetic features of 14 acute lymphoblastic leukemia (ALL) patients with 1; 19 translocation. Ten patients had poor prognostic factors such as age over 10 years, hyperleukocytosis over 5 X 10(4)/microliters or high serum lactic dehydrogenase levels over 5,000 IU/l. Two patients had relapsed within 12 months after the onset, but their 5-year survival rate was 84.6%. Cytogenetically, 6 of 14 patients had multiple subclones. Two had the clones with hyperdiploidy greater than 50 chromosomes, which was known to be one of the favorable prognostic factors in childhood ALL. These findings show ALL children with 1; 19 translocation have a more favorable outcome in spite of some high-risk features than hitherto been thought.

摘要

我们研究了14例伴有1;19易位的急性淋巴细胞白血病(ALL)患者的临床和细胞遗传学特征。10例患者具有不良预后因素,如年龄超过10岁、白细胞增多超过5×10⁴/微升或血清乳酸脱氢酶水平高于5000 IU/L。2例患者在发病后12个月内复发,但其5年生存率为84.6%。细胞遗传学方面,14例患者中有6例有多个亚克隆。2例有超二倍体大于50条染色体的克隆,这是儿童ALL已知的有利预后因素之一。这些发现表明,伴有1;19易位的ALL儿童尽管有一些高危特征,但预后比迄今认为的更有利。

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