期刊文献+

家族性卵巢癌综合征研究进展 被引量:2

下载PDF
导出
摘要 为了解家族性卵巢癌综合征(FOCS)的研究进展,利用MEDLINE等检索复习近5年国外相关英文文献。FOCS患者由于肿瘤抑制基因发生种系突变卵巢癌发生率很高,BRCA是最多见的突变基因。家族性卵巢癌以浆液性癌为主。目前治疗方法首推预防性卵巢切除(BPO),但临床效果尚无最终的令人信服的结论。建议对FOCS患者应行BPO,术后应用激素替代治疗,随访早期发现原发性腹膜浆液性乳头状腺癌。对不愿接受该术者更应密切随访,定期卵巢癌筛查。
作者 李东至
机构地区 广州市妇婴医院
出处 《国外医学(妇产科学分册)》 2003年第2期105-108,共4页 Foreign Medical Sciences(Obstet Gynecol Fascicle)
  • 相关文献

参考文献20

  • 1Gayther SA,Russell P,Harrington P,et al.The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer:No evidence for other ovarian cancer-susceptibility genes.Am J Hum Genet,1999,65:1021-1029
  • 2Boyd J.Molecular genetics of hereditary ovarian cancer.Oncology,1998,12:399-406
  • 3Phillips KA,Nichol K,Ozcclik H,et al.Frequency of p53 mutations in breast carcinomas from Ashkenazi Jewish carriers of BRCA1 mutations.J Natl Cancer Inst,1999,91:469-473
  • 4Narod SA,Boyd J.Current understanding of the epidemiology and clinical implications of BRCA1 and BRCA2 mutations for ovarian cancer.Curr Opin Obstet Gynecol,2002,14:19-26
  • 5Piver MS.Hereditary ovarian cancer.Lessons from the first twenty years of the Gilda Radner Familial Ovarian Cancer Registry.Gynecol Oncol,2002,85:9-17
  • 6Bandera CA,Muto MG,Schorge JO,et al.BRCA1 gene mutations in women with papillary serous carcinoma of the peritoneum.Obstet Gynecol,1998,92(4 Pt 1):596-600
  • 7Karlan BY,Baldwin RL,Lopez-Luevanos E,et al.Peritoneal serous papillary carcinoma,a phenotypic variant of familial ovarian cancer:implications for ovarian cancer screening.Am J Obstet Gynecol,1999,180:917-928
  • 8Rebbeck TR,Lynch HT,Neuhausen SL,et al.Prophylactic oophorectomy in carriers of BRCA1 or BRCA2 mutations.N Engl J Med,2002,346:1616-1622
  • 9Kauff ND,Satagopan JM,Robson ME,et al.Risk-reducing salpingooophorectomy in women with a BRCA1 or BRCA2 mutation.N Engl J Med,2002,346:1609-1615
  • 10Grann VR,Jacobson JS,Thomason D,et al.Effect of prevention strategies on survival and quality-adjusted survival of women with BRCA1/2 mutations:an updated decision analysis.J Clin Oncol,2002,20:2520-2529

同被引文献9

  • 1Pisano M, Coypu A, Persico I, et al. Identification of a founder BRCA2 mutation in sardinia[ J ]. British Journal of Cancer, 2000,82:553-559.
  • 2Schildkraut JM, Thompson WD. Familial ovarian cancer: a population- based case control study[J]. Am J Epidemiol, 1988,128 (3):456.
  • 3Watson P, Lynch HT. Hereditary ovarian cancer ( A 1. Sharp, Mason, e- ds. Ovarian cancer, biology, diagnosis and management [ M ]. London : Chapman and Hall Medical, 1992:9 - 24.
  • 4Chen S, Iversen ES, Friebel T, et al. Characterization of BRCA1 and BRCA2 mutations in a large United States sample [ J ]. Clin Oncol, 2006,24(6) :863.
  • 5Lynch HT, Lynch J F, Conway T A. Hereditary ovarian cancer In ovari- an cancer( RubinSC, Sutton GP, eds) [ M ]. NewYork : McGraw-Hill, 1993 : 189 ~ 217.
  • 6乔丽雅,王振国,张江琴,范敏,成争先.遗传性乳腺癌-卵巢癌临床分析[J].中国优生与遗传杂志,2010,18(5):135-136. 被引量:2
  • 7陆药丹,丁彦青,罗深秋.癌家族及家族性癌三家系[J].中华医学遗传学杂志,2000,17(2):144-144. 被引量:2
  • 8王丹丹,李燕华,张競.卵巢癌组织中HE4表达及与其临床病理因素的关系[J].实用癌症杂志,2012,27(6):578-582. 被引量:15
  • 9孙玲,孙慧,刘林湘,张秋堂,乐晓平,邹典斌,张钦宪.急性白血病ATM基因和BRCA2基因的杂合性缺失[J].临床血液学杂志,2002,15(2):54-56. 被引量:2

引证文献2

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部