Evaluation of coeliac trunk and hepatic artery variations in thoracic CT angiography in patients with congenital heart disease

Kemal Bugra Memis , Hasan Bulut , Hasibe Gokce Cinar , Berna Ucan , Cigdem Uner , Ozkan Kaya , Sonay Aydin
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Abstract

Introduction

Understanding the variations of abdominal vascular structures is important for preventing complications of abdominal surgical procedures for gastrointestinal disease such as necrotizing enterocolitis or others that may arise in patients with congenital cardiac disease. We analysed the coeliac trunk and its branches in children with congenital heart disease to determine whether there is a greater prevalence of associated vascular abnormalities.

Methods

We retrospectively analysed thoracic computed tomography (CT) angiograms performed in our hospital in paediatric patients with congenital heart disease. We documented the anatomical variations observed in abdominal sections in which the coeliac trunk and hepatic arteries were included in the field of view. We used the Uflacker classification to describe anatomical variants of the coeliac trunk, and the Michels classification and its modified version (Hiatt classification) to describe the anatomy of the hepatic artery system.

Results

Our study included 178 patients with congenital heart disease. We identified coeliac trunk variants in 10.7% of the patients. Gastrosplenic trunk was to the most prevalent variant, amounting to 5.6% of total cases. We found hepatic artery variations in 19.1% of the patients. According to the Michels classification, the prevalence of accessory left hepatic artery arising from the left gastric artery as 4.5%, compared to 6.7% based on the Hiatt classification.

Conclusion

The prevalence of coeliac trunk and hepatic artery variations in patients with congenital heart disease was not greater in our study compared to other series in the literature. Clinicians must be vigilant about the variations detected in multislice CT scans to avoid complications resulting from vascular abnormalities, especially in patients who undergo abdominal surgery.

Abstract Image

评估先天性心脏病患者胸部 CT 血管造影中的腹腔干和肝动脉变异。
导言:了解腹部血管结构的变化对于预防胃肠道疾病腹部外科手术并发症(如坏死性小肠结肠炎)或先天性心脏病患者可能出现的其他并发症非常重要。我们对先天性心脏病患儿的腹腔干及其分支进行了分析,以确定相关血管异常的发生率是否更高:方法:我们回顾性分析了本医院为先天性心脏病儿科患者所做的胸部计算机断层扫描(CT)血管造影。我们记录了在腹部切片中观察到的解剖变异,其中腹腔干和肝动脉被纳入视野。我们使用 Uflacker 分类法描述腹腔干的解剖变异,使用 Michels 分类法及其改进版(Hiatt 分类法)描述肝动脉系统的解剖:我们的研究包括 178 名先天性心脏病患者。我们发现10.7%的患者存在腹腔干变异。胃脾动脉干是最常见的变异,占病例总数的 5.6%。我们发现19.1%的患者存在肝动脉变异。根据米歇尔斯(Michels)分类法,由左胃动脉产生的左肝附属动脉的发病率为 4.5%,而根据希阿特(Hiatt)分类法,这一比例为 6.7%:结论:与其他文献相比,我们的研究中先天性心脏病患者腹腔干和肝动脉变异的发生率并不高。临床医生必须对多层 CT 扫描中发现的变异保持警惕,以避免血管异常导致的并发症,尤其是在接受腹部手术的患者中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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