Altinsoy Hasan Baki, Alatas Ozkan, Khalil Emjed, Kara Kenan Abdurrahman, Okten Candan Cudi, Dogan Omer Faruk
Department of Radiology, Health Sciences University, Elazig Research and Training Hospital, Elazig, Turkey.
Department of Cardiovascular Surgery, Health Sciences University, Dr. Cengiz Aslan Research and Training Hospital, Gaziantep, Turkey.
Open Cardiovasc Med J. 2018 Mar 30;12:18-28. doi: 10.2174/1874192401812010018. eCollection 2018.
Popliteal artery entrapment syndrome (PAES) is a very rare pathology that can cause lower extremity ischemia in healthy young people. Anomalous anatomic relationships between the popliteal artery (PA) and the surrounding musculo-tendinous structures cause PAES. We present 31 patients with PAES in 35 limbs that were treated surgically in our clinic within a 12-year period.
From 2001 to 2015, 31 patients (mean age: 32 ± 7.4 years) underwent surgery for PAES. ; 4 patients presented had bilateral PAES. Doppler ultrasonography (US), magnetic resonance angiography (MRA), and conventional angiography were performed as diagnostic procedures. We detected Type I PAES in 4 limbs and Type II PAES in 12 limbs. In the remaining 19 limbs, we diagnosed Type III or Type IV PAES. Simple release of the PA, PA embolectomy and simple release, and the radial artery (RA) patch angioplasty, with or without thromboendarterectomy (TEA), were performed. In 12 limbs, PA continuity was provided by RA interposition.
With the exception of 5 patients, no complications were seen after surgery. Haematoma was detected in 2 patients and local infection in 2 patients. One patient required a revision for recurrent PA thromboembolic event 12 h after surgery. At a median follow- up of 23 months (range: 11-29 months), there were no postoperative complications.
PAES can result in lower limb ischemia due to chronic vascular trauma in young healthy patients. The use of diagnostic tools such as US, a non-invasive method, and MRA are effective diagnostic tools for early diagnosis. With their combined approach, exact and early diagnosis can be achieved. PA release, alone or with arterial bypass using RA, is a viable treatment option when intervention is necessary to prevent limb loss in the early stages of the disease.
腘动脉压迫综合征(PAES)是一种非常罕见的疾病,可导致健康年轻人下肢缺血。腘动脉(PA)与周围肌肉肌腱结构之间异常的解剖关系导致PAES。我们报告了12年间在我们诊所接受手术治疗的35条肢体的31例PAES患者。
2001年至2015年,31例患者(平均年龄:32±7.4岁)接受了PAES手术;4例患者为双侧PAES。采用多普勒超声(US)、磁共振血管造影(MRA)和传统血管造影作为诊断方法。我们在4条肢体中检测到I型PAES,在12条肢体中检测到II型PAES。在其余19条肢体中,我们诊断为III型或IV型PAES。进行了PA的简单松解、PA取栓术和简单松解,以及桡动脉(RA)补片血管成形术,伴或不伴血栓内膜切除术(TEA)。在12条肢体中,通过RA插入维持PA的连续性。
除5例患者外,术后未见并发症。2例患者检测到血肿,2例患者出现局部感染。1例患者术后12小时因复发性PA血栓栓塞事件需要再次手术。中位随访23个月(范围:11 - 29个月),无术后并发症。
PAES可导致年轻健康患者因慢性血管损伤而出现下肢缺血。使用US等非侵入性诊断工具以及MRA是早期诊断的有效诊断工具。通过联合使用这些方法,可以实现准确的早期诊断。当有必要在疾病早期进行干预以防止肢体丧失时,PA松解术单独或联合使用RA进行动脉搭桥术是一种可行的治疗选择。