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在多排螺旋计算机断层血管造影中发现肝动脉的罕见变异与胃十二指肠动脉的可变起源相关。

Rare variations of hepatic arteries in association with variable origin of gastroduodenal artery found in multidetector computed tomography angiography.

作者信息

Skórzewska A, Stajgis P, Grzymisławska M, Rojewska M, Krajecki M, Bruska M, Juszkat R

机构信息

Department of Anatomy, University of Medical Sciences, Poznan, Poland.

出版信息

Folia Morphol (Warsz). 2014 Nov;73(4):531-5. doi: 10.5603/FM.2014.0082.

Abstract

Three rare anatomical variations were found during study on hepatic arterial vascularisation in multidetector computed tomography angiography. In the first described variation the common hepatic artery (CHA) arises from the celiac trunk (CTr) and supplies right hepatic lobe. The left lobe of the liver is supplied by aberrant left hepatic artery originating as a common trunk with the left gastric artery and the splenic artery. This variation may correspond to the type 2 in Michels' classification coexisting with one of three possible patterns of the CTr division (when the CHA is the first branch of the CTr and the gastrosplenic trunk is the second one). The second variation corresponds to the very early bifurcation of the CHA arising from the CTr. Both, the right and left hepatic arteries originate separately from the CTr. The gastroduodenal artery (GDA) originates from the left hepatic artery. It may be regarded as the variation of most common type 1 according to Michels. In the third case the CHA gives raise to the GDA and terminates as the right hepatic artery supplying the right lobe of the liver only. The proper hepatic artery is missing and the left hepatic artery arises from the GDA. This variation does not correspond to any types of Michels' classification.

摘要

在多排螺旋计算机断层血管造影术对肝动脉血管化的研究过程中发现了三种罕见的解剖变异。在第一种描述的变异中,肝总动脉(CHA)起源于腹腔干(CTr)并供应右肝叶。肝左叶由异常的左肝动脉供应,该动脉与胃左动脉和脾动脉共同起源于一个主干。这种变异可能对应于Michels分类中的2型,与CTr分支的三种可能模式之一共存(当CHA是CTr的第一分支且胃脾干是第二分支时)。第二种变异对应于起源于CTr的CHA的极早期分叉。肝右动脉和肝左动脉均分别起源于CTr。胃十二指肠动脉(GDA)起源于肝左动脉。根据Michels的分类,它可被视为最常见的1型变异。在第三种情况中,CHA发出GDA并仅作为供应肝右叶的肝右动脉终止。肝固有动脉缺失,肝左动脉起源于GDA。这种变异不符合Michels分类的任何类型。

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