國家衛生研究院 NHRI:Item 3990099045/5271
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 12145/12927 (94%)
造访人次 : 907348      在线人数 : 910
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜寻范围 查询小技巧:
  • 您可在西文检索词汇前后加上"双引号",以获取较精准的检索结果
  • 若欲以作者姓名搜寻,建议至进阶搜寻限定作者字段,可获得较完整数据
  • 进阶搜寻
    主页登入上传说明关于NHRI管理 到手机版


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: http://ir.nhri.org.tw/handle/3990099045/5271


    题名: PDGFRA one nucleotide deletion: A novel mutation of systemic mastocytosis associated with chronic myelomonocytic leukemia
    作者: Wu, YY;Nieh, SW;Chen, LT;Chan, H;Sheu, LF;Chao, TY;Chen, YC
    贡献者: National Institute of Cancer Research
    摘要: Background: The mast cell is a common tissue cell located in connective tissue around blood vessels and beneath the capsular tissues of most organs. Uncontrolled proliferation can lead to mast cell disease, which may have different clinical presentation depending on site of primary involvement. Recently, a point mutation in the c-kit receptor gene, Asp816Val (D816V), was shown to activate c-kit, via ligand-independent receptor autophosphorylation resulting in uncontrolled mast cell proliferation. Fusion gene involving Fip1-like 1(FIPL1L1) and plateletderived growth factor receptorα (PDGFRA) was identified in hypereosinophilic syndrome (HES) and mast cell disease. These mutations might have quite different treatment response to imatinib mesylate. Case Report: A 71-year-old man presented with intractable ascites, hepatosplenomegaly, and skin ecchymosis change. Laboratory tests showed leukocytosis, monocytosis, and anemia. Histopathological examination of bone marrow, liver, skin, and ascites all showed spindle-shaped mast cells infiltration. Gene mutation analysis revealed one nucleotide deletion in PDGFRA exon18; the frame-shift generating a new mutated protein. The patient was treated with hydroxyurea. His ascites and leukocytosis were under controlled. Conclusions: Systemic mastocytosis should be considered as one cause of ascites, especially in those patients with unexplained hepatomegaly and splenomegaly. Genetic analysis is crucial in this kind of cases in order to determine the treatment strategy and evaluate patients' prognosis.
    日期: 2008
    關聯: American Journal of Case Reports. 2008;9:10-14.
    Link to: http://www.journals.indexcopernicus.com/abstracted.php?level=5&icid=690770
    Cited Times(Scopus): http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=78249235645
    显示于类别:[陳立宗] 期刊論文
    [詹宗晃(2000-2008)] 期刊論文

    文件中的档案:

    档案 描述 大小格式浏览次数
    SCP78249235645.pdf714KbAdobe PDF467检视/开启


    在NHRI中所有的数据项都受到原著作权保护.

    TAIR相关文章

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回馈