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先天性门体分流诊治进展 被引量：8

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摘要 先天性门体分流（congenital portosystemic shunts,CPS）是一种门静脉系统的发育性畸形,Abernethy[1]于1793年对1例死因不明的10个月女婴尸体解剖时首次发现,该疾病可造成门静脉血液流入体静脉系统.一般认为该畸形产生于胚胎发育的第四周到第八周（该阶段为肝静脉和体静脉的发育阶段）,因此该畸形也常与其他心脏和血管畸形相关联.目前,该畸形经典分型分为两型：端-侧分流（Ⅰ型）和侧-侧分流（Ⅱ型）.各型无标准化的治疗方案,主要治疗方式包括手术和介入治疗.本文就门体分流的胚胎发育学、病理、一般症状、并发症、影像学检查以及治疗进展等情况进行综述.
作者 黄顺根
机构地区 苏州大学附属儿童医院外科
出处 《临床外科杂志》 2013年第8期646-649,共4页 Journal of Clinical Surgery
关键词 先天性疾病 门体静脉 血管畸形
分类号 R681.8 [医药卫生—骨科学]
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参考文献40

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同被引文献50

  • 1吴碧君,周苏晋.肝内门-体静脉分流的彩色多普勒超声诊断[J].中华临床医师杂志（电子版）,2012,6(20):204-205. 被引量：1
  • 2陈勇,赵剑波,申鹏,曾庆乐,韦传军,王江云,邱发东,李彦豪.Abernethy畸形的影像学表现[J].中华放射学杂志,2005,39(8):874-876. 被引量：22
  • 3黄劲柏,徐海波,孔祥泉,史河水,李欣,刘定西.先天性门-腔静脉分流畸形的影像分析[J].实用放射学杂志,2007,23(6):848-850. 被引量：5
  • 4Lautz TB, Tantemsapya N, Rowell E, et al. Management and classification of type 1I congenital portosystemic shunts [J]. J Pedi- atrSurg, 2011, 46(2): 308-314.
  • 5Kim MJ, Ko JS, Seo JK, et al. Clinical features of congenital portosystemic shunt in children [J]. Eur J Pediatr, 2012, 171(2) : 395-400.
  • 6Hara Y, Sato Y, Yamamoto S, et al. Successful laparoscopic division of a patent ductus venosus : report of a case [J]. Surg To- day, 2013, 43(4): 434-438.
  • 7Moubarak E, BouvierA, Boursier J, etal. Portosystemic colla- teral vessels in liver cirrhosis : a three-dimensional MDCT pictorial review [J].Abdomlmaging, 2012, 37 (5): 746-766.
  • 8Franchi-Abella S, Branchereau S, Lambert V, et al. Complica- tions of congenital portosystemic shunts in children: therapeutic options and outcomes [J]. J Pediatr Gastroenterol Nutr, 2010, 51(3): 332-330.
  • 9Ferrero GB, Porta F, Biamino E, et al. Remittent hyperam- monemia in congenital portosystemic shunt [J]. Eur J Pediatr, 2010, 169(3).. 369-372.
  • 10Sokollik C, Bandsma RH, Gana JC, et al. Congenital portosys- temic shunt characterization of a multisystem disease [J]. J Pediatr GastroenterolNutr, 2013, 56(6): 675-681.

引证文献8

二级引证文献12

临床外科杂志
2013年 第8期

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