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Peutz-Jeghers综合征9例临床分析 被引量:4

Peutz-Jeghers Syndrome:Clinical Analysis of 9 Cases
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摘要 目的:提高Peutz-Jeghers综合征(Peutz-Jeghers syndrome,PJS)的诊治水平。方法:通过分析2003年—2011年复旦大学附属中山医院收治的9例PJS患者的临床资料,结合文献复习,探讨PJS的发病机制、临床表现、诊断、治疗及预后。结果:9例患者发病年龄1~49岁,有家族史者5例(56%)。6例1次或多次行内镜下胃肠道息肉切除术,术后其症状明显好转,其中1例并发肠套叠导致小肠部分缺血坏死而行小肠部分切除术;2例因息肉巨大而无法在内镜下将其切除,患者拒绝外科手术治疗自动出院;1例就诊时结肠息肉已癌变并全身多发转移,患者放弃治疗。结论:PJS患者有肿瘤易感性,内镜下行胃肠道息肉切除术和定期随访可降低息肉引起的并发症的发生率,并降低患者发生恶性肿瘤的风险。 Objective:To improve the the diagnosis and treatment of Peutz-Jeghers syndrome. Methods:The clinical data of 9 patients with Peutz-Jeghers syndrome hospitalized in Zhongshan Hospital, Fudan University from 2003 to 2011 was retrospec- tively analyzed. Results: The age of onset ranged from 1 to 49 years old. Among them, 5 cases (560%) had family histories. Six cases underwent endoscopic mucosal resection of polyps once or repeatedly, and one of them underwent small intestinal resec- tion because of ischemic necrosis of small intestine caused by intussusception. Two cases who had to undergo surgical operation for the huge polyps denied treatment. One case developed polyp carcinoma. Conclusion: Patients with Peutz-Jeghers syndrome are more susceptible for tumors. Endoscopic therapy and regular follow-up are sound ways to reduce the incidence of complica- tions of Peutz-Jeghers syndrome, as well as to reduce the risk of malignant tumor.
作者 黄畅熹 蔡瑜
出处 《中国临床医学》 2012年第4期377-378,共2页 Chinese Journal of Clinical Medicine
关键词 PEUTZ-JEGHERS综合征 诊断 治疗 Peutz-J eghers syndrome Diagnosis Treatment
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  • 1Giardiello FM, Trimbath JD. Peutz-Jeghers syndrome and man-agement recommendations [J]. Clin Gastroenterol Hepatol,2006,4(4):408-415.
  • 2戴益琛,宋于刚,肖冰,谢军培,曾伟.黑斑息肉综合征临床病理研究52例[J].武警医学,2008,19(5):450-452. 被引量:12
  • 3Robinson J, Lai C, Martin A, et al. Oral rapamycin reducestumour burden and vascularization in Lkbl + /- mice[J]. JPathol, 2009,219(1):35-40.
  • 4Trojan J, Brieger A, Raedle J, et al. Peutz-Jeghers syndrome:molecular analysis of a three generation kindred with a noveldefect in theserine threonine kinase gene STK11 [J]. Am JGastroenterol,1999,94(1) :257-261.
  • 5王振军,严仲瑜,万远廉,刘玉村,吕有勇,徐文怀,黄莚庭.黑斑息肉病LKB1基因胚系突变和肿瘤易感性研究[J].中国胃肠外科杂志,2000,3(2):82-84. 被引量:17
  • 6Beggs AD, Latchford AR, Vasen HF, et al. Peutz-Jeghersagement[J]. Gut, 2010, 59(7):975-986.
  • 7顾国利,魏学明,徐丽梅,王石林.Peutz-Jeghers综合征预防性治疗的研究[J].胃肠病学和肝病学杂志,2012,21(4):380-383. 被引量:26

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  • 1李伟伟,唐坤,李瑞,殷薇薇,郑祥武.Peutz-Jeghers息肉CT诊断价值探讨[J].中华临床医师杂志(电子版),2011,5(15):4547-4550. 被引量:5
  • 2赵鹏,柳建中,董新舒,郝希山.黑斑息肉综合症的治疗-附一家族病例分析[J].中国肿瘤临床,2006,33(4):221-222. 被引量:12
  • 3覃彩团,蒙金兰.清洁灌肠的疗效观察及护理体会[J].现代医药卫生,2006,22(9):1373-1373. 被引量:2
  • 4M Jansen, W W J de Leng, A F Baas, et al. Mu- cosal prolapse in the pathogenesis of Peutz-Jegh- ers polyposis [J]. Gut, 2006, 55(1): 1- 5.
  • 5Francis M Giardiello, Jill D Trimbath. Peutz- Jeghers syndrome and management recommenda- tions [J]. Clinical Gastroenterology and Hepatol- ogy, 2006, 4(4): 408-415.
  • 6Hemminki A, Markie D, Tomlinson I, et al. A serine/threonine kinase gene defective in Peutz - Jeghers syndrome[J]. Nature, 1998, 391(6663) : 184 - 187.
  • 7Spigelman AD, Phillips RKS. Management of the Peutz - Jeghers patient [J]. JR Soc Med, 1989, 82 (11): 681.
  • 8Douglasa corley MU, MD, Johnp Cello. Gastroin- testinal Bleedingand GastricOutletObstruction From Peutz - Jeghers Polyposis Diagnosis and Treatment [J]. WJM, 1997, 166(5):350 - 352.
  • 9Davidson NO. Genetic testing in colorectal cancer: who, when, how and why [J]. Keio J Med, 2007, 56(1) : 14 - 20.
  • 10Van Lier MG, Korsse SE, Mathus- Vliegen EM, et al. Peutz - Jeghers syndrome and family plan- ning: the attitudetowards prenatal diagnosis and pre- implantation genetic diagnosis [J]. Eur J Hum Genet, 2012, 20(2): 236-239.

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