• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

一名患有M2型急性非淋巴细胞白血病且核型为47,XY,t(5;7)(q34;q21), +8的患者的不良预后。

Unfavourable outcome of a patient with M2 acute non lymphocytic leukemia and a 47,XY,t(5;7)(q34;q21), +8 karyotype.

作者信息

Testoni N, Zaccaria A, Celso B, Tura S

机构信息

Centro di Genetica e Citogenetica Oncologica, Istituto di Ematologia L. e A. Seràgnoli, Università di Bologna, Italy.

出版信息

Haematologica. 1991 Jan-Feb;76(1):65-8.

PMID:2055562
Abstract

We report a patient with M2 acute non-lymphocytic leukemia and a complex karyotype: 47,XY,t(5;7)(q34;q21), +8. After chemotherapy with Daunomycin and Arabinosyl Cytosine, a complete remission was reached, but two months later he relapsed and died because of sepsis. Only 5 other cases with translocations involving chromosomes 5 and 7 have been described, but with different breakpoints. Several genes related to cell proliferation and maturation have been identified on the long arms of chromosomes 5 and 7. The possible involvement of specific genes located at or very close to the breakpoints is hypothesized.

摘要

我们报告了一名患有M2型急性非淋巴细胞白血病且核型复杂的患者:47,XY,t(5;7)(q34;q21), +8。在用柔红霉素和阿糖胞苷进行化疗后,患者达到完全缓解,但两个月后复发并因败血症死亡。仅另有5例涉及5号和7号染色体易位的病例被描述,但断点不同。在5号和7号染色体长臂上已鉴定出几个与细胞增殖和成熟相关的基因。推测位于断点处或非常靠近断点的特定基因可能参与其中。

相似文献

1
Unfavourable outcome of a patient with M2 acute non lymphocytic leukemia and a 47,XY,t(5;7)(q34;q21), +8 karyotype.一名患有M2型急性非淋巴细胞白血病且核型为47,XY,t(5;7)(q34;q21), +8的患者的不良预后。
Haematologica. 1991 Jan-Feb;76(1):65-8.
2
Chromosome abnormalities in leukemia and lymphoma.白血病和淋巴瘤中的染色体异常。
Ann Clin Lab Sci. 1983 Mar-Apr;13(2):87-94.
3
5q- and t(2;11) in a patient with M2 acute non-lymphocytic leukemia. Case report.
Haematologica. 1989 Nov-Dec;74(6):595-9.
4
[Abnormal karyotype, t(9;13)(q34;q12) in a patient with acute myelocytic leukemia].
Rinsho Ketsueki. 1988 Nov;29(11):2163-7.
5
11q- and constitutional X trisomy in a patient with M5b acute non-lymphocytic leukemia.一名M5b型急性非淋巴细胞白血病患者存在11号染色体长臂缺失和先天性X三体。
Haematologica. 1993 May-Jun;78(3):185-6.
6
[Acute myeloblastic leukemia 5q-. Clinical and cytogenetic remission by means of intensive chemotherapy].
Sangre (Barc). 1991 Jun;36(3):251-2.
7
Complex chromosome 8;21 translocation with associated hyperdiploidy in acute myeloid leukemia (FAB-M2).急性髓系白血病(FAB-M2)中伴有相关超二倍体的复杂8号;21号染色体易位
Pediatr Blood Cancer. 2008 Mar;50(3):651-4. doi: 10.1002/pbc.21192.
8
[An unusual way of manifesting acute granulocytic leukemia: granulocytic sarcoma of the breast. Apropos of a case with trisomy 22].
Nouv Rev Fr Hematol (1978). 1986;28(2):91-6.
9
Acquired acute myelogenous leukemia after therapy for acute promyelocytic leukemia with t(15;17): a case report and review of the literature.急性早幼粒细胞白血病伴t(15;17)治疗后获得性急性髓系白血病:一例报告并文献复习
P R Health Sci J. 2009 Jun;28(2):146-50.
10
Translocation between chromosome 5q35 and chromosome 11q13-- an unusual cytogenetic finding in a primary refractory acute myeloid leukemia.5号染色体长臂35区与11号染色体长臂13区之间的易位——原发性难治性急性髓系白血病中一种不寻常的细胞遗传学发现。
Clin Lab Haematol. 2006 Jun;28(3):160-3. doi: 10.1111/j.1365-2257.2006.00770.x.