首页> 外文期刊>Annals of anatomy =: Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft >Variations in the anatomy of the celiac trunk: A systematic review and clinical implications
【24h】

Variations in the anatomy of the celiac trunk: A systematic review and clinical implications

机译:腹腔干解剖学的变化:系统评价及其临床意义

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

The normal pattern of the celiac trunk (CT) implies its bifurcation to three branches, the common hepatic, the splenic and the left gastric artery. According to the available literature the CT presents several anatomical variations. The purpose of our study is to investigate the different types of these variations, the corresponding incidences and the probable influence of genetic factors, as they are presented in the existing literature. Four databases were searched for eligible articles for the period up to January 2013 and a total of 36 studies were collected. The CT was trifurcated into the three basic branches in the 89.42% (10,906/12,196) of the cases. Bifurcation of the CT occurred in the 7.40% of the pooled samples (903/12,196). Absence of the CT was the rarest variation with a percentage of 0.38% (46/12,196), hepatosplenomesenteric trunk was found in 49 out of the 12,196 cases (0.40%) and the celiacomesenteric trunk presented an incidence of 0.76% (93/12,196). Other variations of the CT were detected in the 1.64% of the pooled cases (199/12,196). The 14.9% of the cases in the cadaveric series (489/3278 specimens), the 10.5% in the imaging series (675/6501 specimens) and the 4.6% (104/2261) in the liver transplantation series presented variations. These differences are statistically significant (p< 0.001). The Japanese and Korean populations presented more variations in the CT than Caucasians (p< 0.05 and p< 0.001). Negro, colored and black populations presented more variations of the CT than Indian ones (p> 0.05).Using those data, a novel classification of CT variations is proposed.
机译:腹腔干(CT)的正常模式意味着其分叉至三个分支,即肝,脾和胃左动脉。根据现有文献,CT表现出几种解剖学变化。我们研究的目的是调查这些变异的不同类型,相应的发生率以及遗传因素的可能影响,如现有文献中所述。在四个数据库中搜索了截至2013年1月的符合条件的文章,共收集了36篇研究。在89.42%(10,906 / 12,196)的病例中,CT被分为三个基本分支。在合并样本的7.40%(903 / 12,196)中发生了CT分叉。 CT的缺失是最罕见的变异,占0.38%(46 / 12,196),在12196例病例中有49例发现了肝脾腹主干(0.40%),而celencomenteric主干的发病率为0.76%(93 / 12,196)。 。在1.64%的合并病例中检出了CT的其他变异(199 / 12,196)。尸体系列(489/3278标本)中14.9%的病例,影像系列(675/6501标本)中的10.5%和肝移植系列中的4.6%(104/2261)。这些差异具有统计学意义(p <0.001)。与白种人相比,日本人和韩国人的CT差异更大(p <0.05和p <0.001)。与印度人相比,黑人,有色人种和黑人人口的CT变异更多(p> 0.05)。利用这些数据,提出了一种新颖的CT变异分类。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号