Hospital Kuala Lumpur, Department of Surgery, Kuala Lumpur, Malaysia.
Hospital Miri, Department of Surgery, Miri, Sarawak, Malaysia.
Med J Malaysia. 2021 Mar;76(2):270-272.
Iliac aneurysms are rare in children, especially mycotic aneurysms. Re-vascularization is challenging given the infected field and concern on patency due to their growth potential and a longer life-span. We report a complex case of a mycotic iliac aneurysm in a child. A 12-years-old boy with a previous history of infective endocarditis was referred to us for a right common iliac mycotic aneurysm after presenting with pain. A balloon-expandable stent-graft was deployed across the aneurysm during the acute presentation. He improved post-operatively, but developed abdominal pain four weeks later. A repeat computed tomography (CT) imaging showed a new inflammation of the appendix which was adhered to the calcified wall of the aneurysm and an endoleak from the internal iliac artery. A laparotomy was performed and the right internal iliac artery ligated along with an appendicectomy and omental pedicle. Postoperatively the patient was well and discharged home. Six-month surveillance revealed a healthy child and imaging showed a patent stent-graft and no residual collection.
髂动脉瘤在儿童中较为罕见,尤其是感染性动脉瘤。由于感染灶的存在以及对其生长潜力和更长寿命导致的通畅性的担忧,再血管化具有挑战性。我们报告了一例儿童感染性髂动脉瘤的复杂病例。一名 12 岁男孩,既往有感染性心内膜炎病史,因疼痛就诊,被诊断为右侧髂总感染性动脉瘤。在急性发作期间,在动脉瘤处放置了一个球囊扩张支架移植物。术后他情况有所改善,但四周后出现腹痛。重复的 CT 成像显示阑尾有新的炎症,与动脉瘤的钙化壁粘连,并且髂内动脉有内漏。行剖腹手术,结扎右侧髂内动脉,并进行阑尾切除术和网膜蒂。术后患者情况良好并出院回家。6 个月的随访显示患儿健康,影像学检查显示支架移植物通畅,无残留积液。