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发自腹腔干的替代型未分类右肝动脉:一例报告。

Replaced unclassified right hepatic artery arising from the celiac trunk: A case report.

作者信息

Osman Bahaa, Kazan Daniel, Tohme-Noun Carla, Chakhtoura Ghassan, Noun Roger

机构信息

Department of Digestive and Endocrine Surgery, Hotel Dieu de France Hospital, Saint Joseph University, Faculty of Medicine, Beirut, Lebanon.

Department of Radiology, Hotel Dieu de France Hospital, Saint Joseph University, Faculty of Medicine, Beirut, Lebanon.

出版信息

Radiol Case Rep. 2024 Oct 30;20(1):449-453. doi: 10.1016/j.radcr.2024.10.028. eCollection 2025 Jan.

Abstract

Anatomical variations in hepatic arteries are both common and diverse. According to the classic classification systems, a replaced right hepatic artery typically originates from the superior mesenteric artery, supplying blood to the right liver lobe in the absence of the right branch of the proper hepatic artery. This article reports 2 cases of a rare variation, a replaced right hepatic artery arising directly from the celiac trunk. In these cases, the artery courses posterior to the common hepatic artery and then behind the portal vein within the hepatoduodenal ligament. The first case, involving a 62-year-old male with intraductal papillary mucinous neoplasm (IPMN) of the pancreas, was identified intraoperatively during a pancreaticoduodenectomy. The second case, involving a 58-year-old female with chronic sclerosing cholangitis, was detected through contrast-enhanced computed tomography angiography. Identification of such variations is critical in hepatobiliary and pancreatic surgeries to prevent serious postoperative complications. Injury to a replaced right hepatic artery can lead to biliary-enteric anastomosis dehiscence after pancreaticoduodenectomy or ischemic liver complications. While hepatic arteries display numerous anatomical variations, classic classification systems fail to encompass all these anomalies. A more comprehensive classification system, such as CRL and ex-CRL classification, is necessary to ensure safer surgical outcomes.

摘要

肝动脉的解剖变异既常见又多样。根据经典分类系统,替代右肝动脉通常起源于肠系膜上动脉,在肝固有动脉右支缺如的情况下为右肝叶供血。本文报告2例罕见变异,即替代右肝动脉直接起源于腹腔干。在这些病例中,该动脉走行于肝总动脉后方,然后在肝十二指肠韧带内走行于门静脉后方。第一例为一名62岁男性,患有胰腺导管内乳头状黏液性肿瘤(IPMN),在胰十二指肠切除术术中被发现。第二例为一名58岁女性,患有慢性硬化性胆管炎,通过增强CT血管造影检测到。识别此类变异在肝胆胰手术中至关重要,以防止严重的术后并发症。替代右肝动脉损伤可导致胰十二指肠切除术后胆肠吻合口裂开或肝脏缺血性并发症。虽然肝动脉存在众多解剖变异,但经典分类系统未能涵盖所有这些异常。需要一个更全面的分类系统,如CRL和ex-CRL分类,以确保更安全的手术结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2cc/11555244/8a2e6593fde9/gr1.jpg

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