Berhanu Dagim Leykun, Mendere Dereje Berhanu, Chala Zerihun Gadisa, Bekele Fikir Awraris
Department of Surgery, Hawassa University, College of Medicine and Health Sciences, School of Medicine, Hawassa, Ethiopia. Electronic address: https://twitter.com/dagim_leykun.
Department of Surgery, Hawassa University, College of Medicine and Health Sciences, School of Medicine, Hawassa, Ethiopia.
Int J Surg Case Rep. 2025 Jul;132:111456. doi: 10.1016/j.ijscr.2025.111456. Epub 2025 May 21.
True brachial artery aneurysms (TBAA) in children are exceptionally rare vascular anomalies, with fewer than 20 cases of idiopathic isolated aneurysms reported in children aged between 2 month to 18 in the medical literature. We present a rare case of a true brachial artery aneurysm in a 3-year-old child without any associated risk or systemic disease. This case adds to limited literature on TBAA and provides valuable insight for clinician managing similar case in resource limited setting.
A previously healthy 3-year-old female presented with a two-week history of progressive left upper extremity swelling. Physical examination revealed a 2 × 2 cm pulsatile mass on the medial aspect of the left proximal arm, 8 cm proximal to the medial epicondyle. CT angiography (CTA) confirmed a 1.7 × 1.6 cm saccular aneurysm of the proximal brachial artery. The patient underwent successful aneurysm repair with reconstruction using reversed great saphenous vein interposition (GSV) graft. Post-operative recovery was uneventful, with normal vascular function maintained at 3-month follow-up.
This case demonstrates the importance of early recognition and timely surgical management in paediatric arterial aneurysms. A systematic diagnostic approach with ultrasound and CTA enabled precise surgical planning. Histopathology finding support a congenital-idiopathic aneurysm, enriching our understanding of rare paediatric vascular anomalies. Autologous saphenous vein reconstruction was effective, confirming its role as the preferred conduit for paediatric vascular repairs.
Surgical management of paediatric brachial artery aneurysms using autologous vein reconstruction appears safe and effective. Early intervention may prevent potential complications while providing excellent short-term outcomes.
儿童真性肱动脉瘤(TBAA)是极为罕见的血管异常,医学文献中报道的2个月至18岁儿童特发性孤立性动脉瘤病例少于20例。我们报告了一例3岁儿童真性肱动脉瘤的罕见病例,该患儿无任何相关风险因素或全身性疾病。此病例补充了关于TBAA的有限文献,并为资源有限环境下处理类似病例的临床医生提供了有价值的见解。
一名既往健康的3岁女性,有两周进行性左上肢肿胀病史。体格检查发现左上臂近端内侧、内上髁近端8厘米处有一个2×2厘米的搏动性肿块。CT血管造影(CTA)证实肱动脉近端有一个1.7×1.6厘米的囊状动脉瘤。患者接受了成功的动脉瘤修复术,使用大隐静脉倒置移植进行重建。术后恢复顺利,3个月随访时血管功能正常。
本病例证明了小儿动脉性动脉瘤早期识别和及时手术治疗的重要性。超声和CTA的系统诊断方法有助于精确的手术规划。组织病理学结果支持先天性特发性动脉瘤,丰富了我们对罕见小儿血管异常的认识。自体大隐静脉重建有效,证实了其作为小儿血管修复首选管道的作用。
使用自体静脉重建手术治疗小儿肱动脉瘤似乎安全有效。早期干预可预防潜在并发症,同时提供良好的短期疗效。