期刊文献+

多囊肝临床研究进展 被引量:4

Clinical research progress of polycystic liver disease
收藏 分享 导出
摘要 多囊肝全称为常染色体显性遗传性多囊肝病,目前以外科治疗为主。随着对多囊肝病因的研究深入到分子基因水平,分子诊断为实现症状前诊断提供可能。本文主要介绍多囊肝的病因、发病机制、诊断、治疗等方面的研究进展。 The full name of the polycystic liver disease is autosomald ominant polycystic liver disease. Surgical treatment is the main method to deal with it at present. With the deep study of the polycystic liver disease into the molecular genetic level, it is possible for molecular diagnostics to achieve presymptomatic and prenatal diagnosis. The article mainly introduce the research progress of the polycystic liver disease's etiology, pathogenesis, diagnosis, treatment, and so on.
作者 靳松 崔凯 孙自强 李胜 JIN Song, CUI Kai, SUN Zi- qiang, LI Sheng. Department of Hepatobiliary and Vascular Surgery, Affiliated Hospital of Ji' ning Medical College, Ji'ning 272029, China
出处 《国际外科学杂志》 2013年第4期264-267,共4页 International Journal of Surgery
关键词 多囊肝 病因 诊断 治疗 结果 分子诊断技术 Polycystic liver disease Etiology Diagnosis Treatment outcome Molecular diagnostic techniques
作者简介 通讯作者:李胜,Email:drlisheng@sohu.com.
  • 相关文献

参考文献19

  • 1Everson GT, Taylor MR. Management of polycystic liver disease [J]. Cnrr Gastroenterol Rep, 2005, 7( 1 ): 19-25. 被引量:1
  • 2李林,梅长林.多囊肾的诊断及治疗新进展[J].中国医师进修杂志:内科版,2006,29(6):4-6. 被引量:3
  • 3Pehokallio V. Non-parasitic cysts of the liver. A clinical stuffy of 117 cases[J]. Ann Chir Gynaecol Fenn Suppl, 1970, 174: 1-63. 被引量:1
  • 4Reeders ST, Breuning MH, Davies KE, et al. A highly polymor-phic DNA marker linked to adult polycystic kidney disease on chro- mosome 16[J]. Nature, 1985, 317(6037): 542-544. 被引量:1
  • 5Gabow PA. Autosomal dominant polycystic kidney disease [ J ]. N Engl J Med, 1993, 329(5) : 332-342. 被引量:1
  • 6Reynolds DM, Falk CT, Li A, et al. Identification of a locus for autosomal dominant polycystic liver disease, on chromosome 19p13. 2-13. 1 [ J]. Am J Hum Genet, 2000, 67 (6):1598-1604. 被引量:1
  • 7Tahvanainen P, Tahvanainen E, Reijonen H, et al. Polycystic liv- er disease is genetically heterogeneous: clinical and linkage studies in eight Finnish families[ J]. J Hepatol, 2003, 38( 1 ) : 39-43. 被引量:1
  • 8Davila S, Furu L, Gharavi AG, et al. Mutations in SEC63 cause autosomal dominant polycystic liver disease[ J]. Nat Genet, 2004, 36(6) : 575-577. 被引量:1
  • 9Li A, Davila S, Furu L, et al. Mutations in PRKCSH cause isola- ted autosomal dominant polycystic liver disease [ J ]. Am J Hum Genet, 2003, 72(3): 691-703. 被引量:1
  • 10Praetorius HA, Spring KR. The renal cell primary cilium functions as a flow sensor [ J ]. Curr Opin Nephrol Hypertens, 2003, 12 (5) : 517-520. 被引量:1

二级参考文献30

  • 1Martin I, McKinley A, Currie E, et al. Tailoring the management of nonparasitic liver cysts[J]. Ann Surg,1998,228(2): 167-172. 被引量:1
  • 2Tocchi A, Mazzoni G, Costa G, et al. Symptomatic nonpara- sitic liver cysts:options for and results of surgical treatment[J] Arch Surg,2002,137(2) : 154-158. 被引量:1
  • 3LIANG Ting-bo,BAI Xue-li,ZHENG Shu-sen, et al. Deroof of congenital liver cysts,open surgery or laparoscopic approach[J]. Chin J Gen Surg,2006,21(1):23-25. 被引量:1
  • 4Moorthy K,Mihssin N ,Houghton PW.The management of simple hepatic cysts:sclerotherapy or laparoscopic fenestration[J]. Ann R Coil Surg Engl,2001,83(6):409 414. 被引量:1
  • 5Tan YM, Ooi LL, Soo KC, et al. Does laparoscopic fenestration provide long-term alleviation for symptomatic cystic disease of the liver[J]. ANZ J Surg,2002,72(10):743-745. 被引量:1
  • 6Fiamingo P, Tedeschi U, Veroux M, et al. Laparoscopic treatment of simple hepatic cysts and polycystic liver disease [J]. Surg Endosc,2003,17(4):623-626. 被引量:1
  • 7Klingler PJ, Gadenstatter M, Schmid T, et al. Treatment of hepatic cysts in era of laparoscopic surgery[J]. Br J Surg, 1997,84(4) :438-444. 被引量:1
  • 8Basil AJ, Benjamin LJ, Philip CM, et al. Surgical strategy for cystic disease of the liver in a Western Hepatobiliary Center[J]. World J Surg, 2002,26(4) : 462-469. 被引量:1
  • 9Gabow PA. Autosomal dominant polycystic kidney disease. New Eng J Med, 1993,329: 332-342. 被引量:1
  • 10International Polyeystie Kidney Disease Consortium. Polyeystie kidhey disease: the complete structure of PKD1 gene and its protein.Cell, 1994,81: 2189-2198. 被引量:1

共引文献12

同被引文献89

  • 1何玲玲,张俊琦.飞行员多囊肾、多囊肝一例[J].中华航空航天医学杂志,2013(1). 被引量:1
  • 2Bassam Abu-Wasel,Caolan Walsh,Valerie Keough,Michele Molinari.Pathophysiology, epidemiology, classification and treatment options for polycystic liver diseases[J].世界胃肠病学杂志:英文版(电子版),2013,0(35):5775-5786. 被引量:1
  • 3Drenth, Chrispijn, Nagomey, et al. Medical and surgical treatment options for polycystic liver disease[J]. Hepatology, 2010, 52(6): 2223- 2230. 被引量:1
  • 4Onor, Franchitto, Mancinelli, et al. Polycystic liver diseases [J]. Dig Liver Dis, 2010, 42(4): 261-271. 被引量:1
  • 5Everson, Helmke, Doctor. Advances in management ofpolycystic liver disease[J]. Expert Rev G-astroenterol Hepatol, 2008, 2(4): 563-576. 被引量:1
  • 6Chandok. Polycystic liver disease: a clinical review [J]. Ann Hepatol, 2012, 11(6): 819-826. 被引量:1
  • 7Keimpema, Koning, Hoek, et al. Patients with isolated polycystic liver disease referred to liver centres: clinical characterization of 137 cases [J]. Liver Int, 2011, 31 (1): 92-98. 被引量:1
  • 8Temmerman, Missiaen, Bammens, et al. Systematic review: the pathophysioiogy and management of polycystic liver disease [J]. Aliment Pharmacol Ther, 2011, 34(7): 702-713. 被引量:1
  • 9Harris, Torres. Polyeystic kidney disease [J]. Annu Rev Med, 2009, 60 (2): 321-337. 被引量:1
  • 10Xu C, Rossetti S, Jiang L, et al. Human ADPKD primary cyst epithelial ceils with a novel, single codon deletion in the PKD1 gene exhibit defective ciliary polycystin localization and loss of flow-induced Ca2* signaling [J]. Am J Physiol Renal Physiol, 2007, 292(3): F930-945. 被引量:1

引证文献4

二级引证文献6

投稿分析

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 意见反馈