Rosset E, Hartung O, Brunet C, Roche P H, Magnan P E, Mathieu J P, Branchereau A, Farisse J
Laboratoire d'Anatomie, Faculté de Médecine de Marseille, France.
Surg Radiol Anat. 1995;17(2):161-9, 23-7. doi: 10.1007/BF01627578.
We report 15 examples of popliteal artery entrapment syndrome observed in 11 patients. The anatomical causes were as follows: in one case, the popliteal artery presented an aberrant course medially to the medial head of the gastrocnemius muscle. In 5 cases, there was a small fibrous band linking the medial head of the gastrocnemius muscle to the lateral condyle and crossing behind the popliteal artery; in 5 cases this anomaly was also found in association with an abnormally high and/or internal insertion of the medial head of gastrocnemius muscle. In the last 4 cases, there was a muscular insertion anomaly associated with muscular hypertrophy causing arterial compression. Arteriography performed in the 11 patients showed evocative signs of the diagnosis in all cases where the artery was patent. Two popliteal arteries were occluded. CT scan and MRI examination of the popliteal fossa enabled us to define the muscular origin of the popliteal compression. All of the patients were operated upon; two received a reversed saphenous bypass and all of the others were treated by liberation of the popliteal artery and/or vein by a posterior approach. Follow-up in all patients at long term showed good prognosis. All of the patients were able to take up their previous physical activities without sequelae. Our review of the literature, which is based on 374 cases of popliteal artery entrapment observed in 280 patients, made it possible to define the frequency of the various anomalies observed, their symptoms and the different therapeutic possibilities. The multiple anatomical classifications as well as the arterial and muscular embryology are also described.
我们报告了在11例患者中观察到的15例腘动脉压迫综合征病例。解剖学原因如下:1例中,腘动脉走行异常,位于腓肠肌内侧头的内侧。5例中,有一条小纤维带连接腓肠肌内侧头与外侧髁,并在腘动脉后方交叉;5例中还发现这种异常与腓肠肌内侧头异常高位和/或内侧附着有关。在最后4例中,存在与肌肉肥大相关的肌肉附着异常,导致动脉受压。对11例患者进行的动脉造影显示,在所有动脉通畅的病例中均有提示诊断的征象。两条腘动脉闭塞。对腘窝进行CT扫描和MRI检查使我们能够确定腘动脉受压的肌肉起源。所有患者均接受了手术治疗;2例接受了大隐静脉转流术,其他所有患者均采用后路松解腘动脉和/或静脉的方法进行治疗。所有患者的长期随访显示预后良好。所有患者都能够恢复之前的体育活动,没有后遗症。我们基于280例患者中观察到的374例腘动脉压迫病例进行的文献综述,使我们能够确定观察到的各种异常的频率、其症状以及不同的治疗可能性。还描述了多种解剖学分类以及动脉和肌肉的胚胎学。