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撒哈拉以南非洲地区胡桃夹综合征的外科治疗:贝宁六例系列病例的中期结果

Surgical treatment of nutcracker syndrome in Sub-Saharan Africa: Mid-term outcomes from a six-case series in Benin.

作者信息

Bata Abdel Kémal Bori, Gbessi Mahugnon Emmanuel Martino, Ibrahim Ahmad, Gbegnide Caleb, Nékoua Désiré, Gandji Wilfried

机构信息

University Visceral Surgery Clinic (CNHU-HKM), Faculty of Health Sciences, University of Abomey-Calavi, Cotonou, Benin; University Cardiology Clinic (CNHU-HKM), Faculty of Health Sciences, University of Abomey-Calavi, Cotonou, Benin.

University Visceral Surgery Clinic (CNHU-HKM), Faculty of Health Sciences, University of Abomey-Calavi, Cotonou, Benin.

出版信息

Int J Surg Case Rep. 2025 Sep;134:111787. doi: 10.1016/j.ijscr.2025.111787. Epub 2025 Aug 13.

Abstract

INTRODUCTION

Nutcracker syndrome is a rare vascular condition whose management has long been controversial. Data remain scarce in Sub-Saharan Africa. The objective of this study is to report the clinical presentations and mid-term outcomes of patients who underwent surgical treatment for Nutcracker syndrome in Benin.

METHODS

This was a single-center retrospective study conducted from November 2022 to January 2025. It included all patients who underwent surgical management of Nutcracker syndrome at our hospital during this period.

RESULTS

Six cases of Nutcracker syndrome were identified, all in male patients. The median age was 15.5 years [IQR: 13.5-16]. Left flank pain and varicocele were present in all patients. Abdominal Doppler ultrasound and abdominal CT angiography were performed in all cases. The mean aorto-mesenteric angle was 11.8° ± 2.7. The surgical procedure performed was transposition of the left renal vein into the inferior vena cava. Postoperative outcomes were satisfactory, with complete resolution of symptoms and no major complications or deaths during a median follow-up of 9 months [IQR: 8-13].

CONCLUSIONS

Surgery for rare vascular anomalies is feasible in Sub-Saharan Africa with excellent results. This supports advocacy for improved technical infrastructure.

摘要

引言

胡桃夹综合征是一种罕见的血管疾病,其治疗方法长期以来一直存在争议。撒哈拉以南非洲地区的数据仍然很少。本研究的目的是报告在贝宁接受胡桃夹综合征手术治疗的患者的临床表现和中期结果。

方法

这是一项于2022年11月至2025年1月进行的单中心回顾性研究。它纳入了在此期间在我们医院接受胡桃夹综合征手术治疗的所有患者。

结果

共确诊6例胡桃夹综合征患者,均为男性。中位年龄为15.5岁[四分位间距:13.5 - 16岁]。所有患者均有左侧腰痛和精索静脉曲张。所有病例均进行了腹部多普勒超声和腹部CT血管造影。平均腹主动脉 - 肠系膜上动脉夹角为11.8°±2.7°。所施行的手术为左肾静脉转位至下腔静脉。术后结果令人满意,症状完全缓解,在中位随访9个月[四分位间距:8 - 13个月]期间无重大并发症或死亡。

结论

在撒哈拉以南非洲地区,针对罕见血管异常进行手术是可行的,且效果良好。这支持了对改善技术基础设施的倡导。

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