Suppr超能文献

急性髓系白血病中涉及12号染色体短臂的易位:与既往骨髓增生异常及接触诱变剂的关联。英国癌症细胞遗传学组(UKCCG)。

Translocations involving 12p in acute myeloid leukemia: association with prior myelodysplasia and exposure to mutagenic agents. United Kingdom Cancer Cytogenetics Group (UKCCG).

出版信息

Genes Chromosomes Cancer. 1992 Oct;5(3):252-4. doi: 10.1002/gcc.2870050313.

Abstract

Six cases of acute myeloid leukemia (AML) with translocations involving 12p are described. The patients were one child age 7 yrs and five adults with an age range of 20-66 yrs (median 46 yrs). In two patients AML followed treatment for acute lymphoblastic leukemia (ALL), in one case after 11 years disease-free survival. Of the remaining four patients, two had been occupationally exposed to possible mutagens and three had a previous myelodysplastic phase. Two patients achieved complete remission; survival for the six cases was between 1 and 24 months (median 6.5 months). The breakpoints in 12p occurred in p11, p12, and p13, indicating that several sites are important in these rearrangements, and it is suggested that t(12;17)(p11;q11) is a new nonrandom abnormality in AML.

摘要

本文描述了6例急性髓系白血病(AML)伴有涉及12号染色体短臂(12p)易位的病例。患者包括1名7岁儿童和5名成年人,年龄范围为20 - 66岁(中位年龄46岁)。2例患者在急性淋巴细胞白血病(ALL)治疗后发生AML,其中1例在无病生存11年后出现。其余4例患者中,2例有职业性接触可能诱变剂的情况,3例曾有骨髓增生异常阶段。2例患者实现完全缓解;6例患者的生存期为1至24个月(中位生存期6.5个月)。12p上的断点发生在p11、p12和p13,表明这些位点在这些重排中很重要,提示t(12;17)(p11;q11)是AML中一种新的非随机异常。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验