Cañizares Otero Maria Carla, Osterman Floyd, Danckers Mauricio
Department of Medicine, HCA Florida Aventura Hospital, Aventura, FL, USA.
Department of Radiology, HCA Florida Aventura Hospital, Aventura, FL, USA.
AME Case Rep. 2022 Jul 25;6:28. doi: 10.21037/acr-22-9. eCollection 2022.
Iliac artery aneurysms (IAA) can exist in isolation or in combination abdominal aortic aneurysmal disease. Isolated IAA are rare, often asymptomatic and will present with compression of local structures or incidentally on imaging. Treatment depends on symptomology and size. While endovascular repair has become the preferred method in recent years, for patients with extensive aneurysmal disease, the standard of care is surgical procedure. Acute limb ischemia (ALI) related to aneurysmal disease can occur by progression of untreated disease or rarely, as a complication of its repair.
A man in his 70s who had previously undergone aorto-bifemoral repair for severe aorto-iliac aneurysmal disease nine years prior presented to the emergency department (ED) with a cold left lower extremity concerning for ALI. Emergent aortogram revealed progression of aneurysmal disease with extrinsic graft compression by a giant left iliac aneurysm and femoral artery thrombosis. He underwent femoral artery thrombectomy, bilateral graft limb stent placement and left femoral graft anastomosis balloon angioplasty with stent placement achieving restoration of limb flow and resolution of symptoms. He was discharged and unfortunately lost in follow up. He returned eight months later with mixed shock due to a ruptured left iliac aneurysm. Despite aggressive treatment measures, patient progressed to multi-organ failure, cardiopulmonary arrest, and death.
Our case illustrates an unusual mechanism of ALI by extrinsic graft compression from an expanding left IAA over the course of eight years through delayed retrograde collateral flow. It highlights its life-threating late complications and the importance of close follow-up after abdominal aneurysm surgical repair.
髂动脉瘤(IAA)可单独存在,也可与腹主动脉瘤疾病并存。孤立性IAA较为罕见,通常无症状,会表现为对局部结构的压迫或在影像学检查时偶然发现。治疗取决于症状和大小。近年来,血管腔内修复已成为首选方法,但对于患有广泛动脉瘤疾病的患者,标准治疗方法是外科手术。与动脉瘤疾病相关的急性肢体缺血(ALI)可因未治疗疾病的进展而发生,或很少作为其修复的并发症出现。
一名70多岁的男性,9年前因严重的主-髂动脉瘤疾病接受了主-双股动脉修复术,现因左下肢发冷至急诊科就诊,怀疑为ALI。急诊主动脉造影显示动脉瘤疾病进展,巨大的左髂动脉瘤对外侧移植物造成压迫,且股动脉血栓形成。他接受了股动脉血栓切除术、双侧移植物肢体支架置入术以及左股移植物吻合口球囊血管成形术并置入支架,实现了肢体血流恢复和症状缓解。他出院了,但不幸的是失访了。8个月后,他因左髂动脉瘤破裂出现混合性休克再次就诊。尽管采取了积极的治疗措施,患者仍进展为多器官功能衰竭、心肺骤停并死亡。
我们的病例说明了一种不寻常的ALI机制,即扩张的左IAA通过延迟的逆行侧支血流在8年时间里对外侧移植物造成压迫。它突出了其危及生命的晚期并发症以及腹主动脉瘤手术修复后密切随访的重要性。