Duymaz Senanur, Duymaz Burak, Gursan Onur, Kosay M Can
Department of Cardiovascular Surgery, Dokuz Eylul University Faculty of Medicine, Izmir, Türkiye.
Department of Orthopedics and Traumatology, Dokuz Eylul University Faculty of Medicine, Izmir, Türkiye.
Front Pediatr. 2025 May 23;13:1560952. doi: 10.3389/fped.2025.1560952. eCollection 2025.
Popliteal artery pseudoaneurysms are rare but potentially life-threatening complications following orthopedic procedures, particularly osteotomies. These pseudoaneurysms, characterized by a hematoma caused by disruption of the arterial wall and contained by surrounding tissues rather than all arterial layers, can cause severe ischemic damage if not promptly diagnosed and treated. Early detection and timely surgical intervention are critical to prevent catastrophic outcomes such as thrombosis, embolization, or limb loss. This case highlights the challenges in diagnosing and managing a delayed popliteal artery pseudoaneurysm caused by implant migration in a pediatric patient.
A 15-year-old male patient with cerebral palsy presented with sudden, severe knee pain and localized swelling around the knee joint. These symptoms occurred two years after he underwent a distal femoral extension osteotomy with lateral plate fixation. Initial imaging studies were inconclusive, suggesting possibilities such as soft tissue sarcoma or hematoma. However, an incisional biopsy unexpectedly revealed a pseudoaneurysm cavity adjacent to the popliteal artery. Further imaging identified that the distal screws of the femoral plate had migrated posteriorly due to femoral deformity, causing direct irritation and injury to the artery.
An urgent multidisciplinary surgical approach was implemented. The procedure began with femoral artery clamping to control bleeding, followed by excision of the pseudoaneurysm cavity. A saphenous vein graft was harvested and interposed to repair the damaged segment of the popliteal artery. To eliminate the source of irritation, the screws were removed. Postoperative ultrasonography confirmed successful arterial repair, with no signs of thrombosis or recurrence. The patient was mobilized early and discharged with an antiplatelet regimen, followed by regular clinical monitoring.
This case emphasizes the importance of routine follow-up in pediatric patients with orthopedic implants, as skeletal growth and deformity progression can lead to implant migration and serious vascular complications. The delayed diagnosis underscores the need for heightened clinical suspicion and comprehensive imaging in patients with unusual postoperative symptoms. Early recognition and timely multidisciplinary surgical intervention are crucial for preventing life-threatening vascular injuries. This case also highlights the necessity of individualized implant removal planning in growing patients to avoid similar complications.
腘动脉假性动脉瘤是骨科手术后罕见但可能危及生命的并发症,尤其是截骨术后。这些假性动脉瘤的特征是动脉壁破裂导致血肿,由周围组织而非所有动脉层包裹,如果不及时诊断和治疗,可导致严重的缺血性损伤。早期发现和及时的手术干预对于预防诸如血栓形成、栓塞或肢体丧失等灾难性后果至关重要。本病例突出了诊断和处理一名儿科患者因植入物移位导致的延迟性腘动脉假性动脉瘤的挑战。
一名15岁脑瘫男性患者,在接受股骨远端延长截骨术并使用外侧钢板固定两年后,突然出现严重的膝关节疼痛和膝关节周围局部肿胀。最初的影像学检查结果不明确,提示可能是软组织肉瘤或血肿等情况。然而,切开活检意外发现腘动脉旁有一个假性动脉瘤腔。进一步的影像学检查发现,由于股骨畸形,股骨钢板的远端螺钉向后移位,直接刺激并损伤了动脉。
实施了紧急的多学科手术方法。手术首先夹闭股动脉以控制出血,随后切除假性动脉瘤腔。采集大隐静脉进行移植,修复腘动脉受损段。为消除刺激源,取出了螺钉。术后超声检查证实动脉修复成功,无血栓形成或复发迹象。患者早期即可活动,并在服用抗血小板药物的情况下出院,随后进行定期临床监测。
本病例强调了对接受骨科植入物的儿科患者进行常规随访的重要性,因为骨骼生长和畸形进展可能导致植入物移位和严重的血管并发症。延迟诊断凸显了对术后出现异常症状的患者提高临床怀疑度和进行全面影像学检查的必要性。早期识别和及时的多学科手术干预对于预防危及生命的血管损伤至关重要。本病例还突出了对生长中的患者进行个性化植入物取出计划以避免类似并发症的必要性。