Case Reports in Vascular Medicine

Case Reports in Vascular Medicine / 2019 / Article

Case Report | Open Access

Volume 2019 |Article ID 8540631 |

Viktor Labmayr, Aryan Aliabadi, Kurt Tiesenhausen, Marianne Brodmann, Florian Schmid, Dana Moore, "Popliteal Artery Entrapment Syndrome (PAES) in a 17-Year-Old Adolescent", Case Reports in Vascular Medicine, vol. 2019, Article ID 8540631, 4 pages, 2019.

Popliteal Artery Entrapment Syndrome (PAES) in a 17-Year-Old Adolescent

Academic Editor: Antonio Silvestro
Received07 Jan 2019
Accepted25 Feb 2019
Published11 Mar 2019


Introduction. Popliteal artery entrapment syndrome (PAES) is caused by compression of the popliteal artery (PA) due to deranged myotendinous structures. It can be asymptomatic or may present with exercise intolerance, claudication, or even limb-threatening ischemia. The clinical picture depends on the anatomy and degree of vascular compromise. Case Description. We report a case of a 17-year-old Caucasian male with PAES Type II presenting with intermittent claudication and progression towards acute limb ischemia. Diagnostics. MRI and MRA helped identifying the aberrant anatomy and thrombotic occlusion. Doppler ultrasound and conventional angiography have also been employed in a stepwise approach. Intervention. The thrombus at the site of occlusion was removed by the use of catheter-directed lysis. Subsequently, popliteal artery release was achieved by myotomy of the aberrant medial head of gastrocnemius muscle (MHGM) and muscle transfer to the medial femoral condyle. A three-month regimen of 60mg edoxaban was recommended after surgery. Outcome. Surgical correction of the anomalous anatomy and postoperative anticoagulation led to freedom of symptoms. Lesson. Clinical presentation of PAES mimicking peripheral artery occlusive disease is very rare but potentially limb-threatening. PAES should be considered in young and otherwise healthy individuals.

1. Introduction

Popliteal artery entrapment syndrome (PAES) is a very rare pathology caused by an abnormal anatomic course of the popliteal artery (PA) and/or the adjacent myotendinous structures of the popliteal region. The clinical picture is highly variable. PAES can be asymptomatic in the case of sufficient collateralization of the PA. However, it can also present with foot paleness, pulselessness, and intermittent or even constant claudication. Its most critical manifestation is acute limb-threatening ischemia. The degree of symptoms depends very much on the underlying morphology. Functional entrapment caused by hyperemic muscle is neither visible in clinical examination nor detectable in Doppler ultrasound study; hence detailed medical history-taking can give the clue for its diagnosis. Partial or complete obstruction of the PA can be initially assessed by taking the pulses or by visualization with ultrasound.

2. Case

We report the case of a previously healthy 17-year-old Caucasian male with exercise-induced pain of the right foot that had deteriorated over the course of three months. During the last week prior to presentation at our emergency department, the symptoms had progressed from intermittent to constant calf pain. At clinical examination, the right foot was pale and cool with delayed capillary refill and absent pedal pulses consistent with the clinical picture of acute limb ischemia. The left foot was warm and well perfused with palpable pedal pulses.

Doppler ultrasound study of the right lower limb showed an occlusion at the proximal part of the right popliteal artery (PA). With magnetic resonance angiography the presence of a four-centimeter thrombus occluding this section of the PA was confirmed.

Furthermore, Doppler ultrasound study of the asymptomatic, contralateral (left) popliteal region revealed an occlusion of the PA with sufficient collateralization and unimpaired three-vessel runoff to the foot.

By conventional transfemoral angiography, the previously identified occlusion of the right PA and its aberrant course were demonstrated again (Figure 1). An attempt of continuous intraarterial thrombolysis of the occluded right PA was undertaken by the use of actilyse and continuous heparin applied via a lysis catheter over 24 hours. The required therapeutic dose was controlled with aPTT between 60 and 80 seconds. This resulted in a significant reduction of thrombotic material within the PA, but the vessel was still considerably occluded (70-80%). After 24 hours of catheter-directed thrombolysis, low-molecular-weight heparin (LMWH) in therapeutic dosage and continuous infusion of iloprost (over 4h) were given daily. Further investigations were started to identify the already suspected extravascular cause of occlusion.

Indeed, in magnetic resonance imaging the anomalous origin of the MHGM lateral to the medial condyle of the femur was detected. The muscle’s tendon and belly crossed over a medialized PA and caused its compression (Figure 2(b)). This aberrant anatomy was present bilaterally, yet asymptomatic on the left side.

Hence, indication for surgical decompression was given. A posterior surgical approach was used to enter the popliteal fossa. The intraoperative anatomy presented as a PAES classification Type II with a popliteal artery course medial to the extremely lateralized MHGM. The artery did not show signs of stenosis or vascular wall hypertrophy; therefore only myotomy at the origin of the MHGM was performed. The artery was moved laterally into the popliteal fossa and the muscle was inserted at the correct position at the posterior surface of the medial femoral condyle.

Postoperatively, the patient recovered well and had a warm, pain-free foot with palpable pedal pulses. A three-month regimen of 60mg edoxaban was recommended after surgery.

3. Discussion

Patients under 40 years of age presenting with arterial occlusive disease of the lower limbs may suffer from a rare disease. Although premature atherosclerosis is the most common problem, claudication with limb-threatening ischemia may result from thromboembolism, Buerger's disease, collagen vascular disease (both autoimmune or hereditary), popliteal artery aneurysm, adventitial cystic disease, and popliteal artery entrapment syndrome [15]. Our patient had a negative history of risk factors associated with arterial occlusive disease and normal laboratory values regarding inflammation or autoimmune disease. Hence, local lumen narrowing due to macroscopic structural changes was highly suspected. In this setting, MRI is key to identifying the culprit. On imaging, the abnormal relationship between the PA and the surrounding myofascial structures of the popliteal fossa gave the hint for diagnosing PAES.

The syndrome can be classified into six subtypes based on the anatomic abnormality. In Type I, the PA runs medial to the normally positioned MHGM. In Type II, the MHGM attaches abnormally more laterally on the medial femoral condyle and medially displaces the PA. In Type III, an abnormal accessory slip arises from the MHGM and entraps the anatomically normal PA. In Type IV, the PA lies deep to the popliteus muscle that causes its compressions. Type V involves both the popliteal artery and vein in any of the before mentioned scenarios. Type IV describes a functional entrapment of the PA caused by an anatomically regular but hypertrophied MHMG [68]. Although not included in this classification, entrapment syndrome may also arise from anomalous origin of the lateral head of the gastrocnemius muscle [9].

This case report is about a patient with PAES Type II that became symptomatic on the right limb and remained asymptomatic on the left limb. Studies report the proportion of bilateral entrapment of the PA ranging between 30 and 74 percent [8, 10, 11], highly emphasizing the need for bilateral diagnostic work-up.

Although intraarterial lysis brought significant reduction of thrombotic occlusion, surgical release of the entrapped PA was necessary. Intraoperatively, the integrity of our patient’s PA could be verified by surgical exploration. Theoretically, constant mechanical compression of the artery by myotendinous structures might have induced sclerosis and aneurysmal degeneration of the arterial wall resulting in stenosis, aneurysm, or occlusion. Given this scenario, further vascular procedures such as venous graft reconstruction, endarterectomy, or bypass grafting would have been necessary [1214]. In this patient, myotomy with restoration of the regular anatomy was sufficient to result in cure and freedom from symptoms in the postoperative course.

We recommended oral anticoagulation to decrease the thrombogenic risk after occlusion caused by entrapment. Hypothetically speaking, compression from outside causes blood flow deceleration and stasis, increasing the risk for thrombotic events. We did not recommend antiplatelet therapy as there is assumedly no endothelial dysfunction in artery entrapment syndrome cascading platelet aggregation.

4. Conclusion

PAES is rare, but knowledge and physicians’ awareness of this condition are crucial to early diagnosis and treatment in cases with possibly limb-threatening claudication. The pathology may affect otherwise young and healthy individuals without cardiovascular risk factors. Interdisciplinary cooperation between several specialists such as angiologists, radiologists, and vascular surgeons is fundamental for optimal patient management.

Conflicts of Interest

The authors declare that they have no conflicts of interest.


  1. M. Jarraya, S. Simmons, A. Farber, O. Teytelboym, N. Naggara, and A. Guermazi, “Uncommon Diseases of The Popliteal Artery: A Pictorial Review,” Insights into Imaging, vol. 7, no. 5, pp. 679–688, 2016. View at: Publisher Site | Google Scholar
  2. V. Tuveson, H. E. Löfdahl, and R. Hultgren, “Patients with abdominal aortic aneurysm have a high prevalence of popliteal artery aneurysms,” Vascular Medicine (United Kingdom), vol. 21, no. 4, pp. 369–375, 2016. View at: Google Scholar
  3. J. G. Gwon, Y.-J. Kwon, Y. J. Han, Y.-P. Cho, and T.-W. Kwon, “Chronic Nonatherosclerotic Occlusive Popliteal Artery Disease,” Annals of Vascular Surgery, vol. 47, pp. 128–133, 2018. View at: Publisher Site | Google Scholar
  4. P. Jud, T. Gary, F. Hafner et al., “Multiple arterial thromboses due to cystic medial degeneration Erdheim-Gsell: A case report,” Medicine (United States), vol. 96, no. 47, Article ID e8782, 2017. View at: Google Scholar
  5. J. W. Hallett Jr., L. H. Greenwood, and J. G. Robison, “Lower extremity arterial disease in young adults. A systematic approach to early diagnosis,” Annals of Surgery, vol. 202, no. 5, pp. 647–652, 1985. View at: Publisher Site | Google Scholar
  6. L. J. Levien and M. G. Veller, “Popliteal artery entrapment syndrome: more common than previously recognized,” Journal of Vascular Surgery, vol. 30, no. 4, pp. 587–598, 1999. View at: Publisher Site | Google Scholar
  7. N. M. Rich, G. J. Collins, and P. T. J. McDonalt, “Popliteal vascular entrapment,” JAMA Surgery, vol. 114, no. 12, pp. 1377–1394, 1979. View at: Publisher Site | Google Scholar
  8. J. W. Love and T. J. Whelan, “Popliteal artery entrapment syndrome,” The American Journal of Surgery, vol. 109, no. 5, pp. 620–624, 1965. View at: Publisher Site | Google Scholar
  9. M. D. Chang, A. Steer, W. Perera, and D. R. Robinson, “Bilateral popliteal artery entrapment syndrome secondary to anomalous lateral heads of gastrocnemius,” ANZ Journal of Surgery, vol. 87, no. 10, pp. E149–E150, 2017. View at: Publisher Site | Google Scholar
  10. P. S. Collins, P. T. McDonald, and R. C. Lim, “Popliteal artery entrapment: An evolving syndrome,” Journal of Vascular Surgery, vol. 10, no. 5, pp. 484–490, 1989. View at: Publisher Site | Google Scholar
  11. L. Corneloup, C. Labanère, L. Chevalier et al., “Presentation, diagnosis, and management of popliteal artery entrapment syndrome: 11 years of experience with 61 legs,” Scandinavian Journal of Medicine & Science in Sports, vol. 28, no. 2, pp. 517–523, 2018. View at: Publisher Site | Google Scholar
  12. E. J. Lee, J. S. Jung, K. Lee, S. H. Lee, H. S. Son, and K. Sun, “Popliteal artery entrapment syndrome: A case with bilateral different types,” The Korean Journal of Thoracic and Cardiovascular Surgery, vol. 47, no. 3, pp. 302–305, 2014. View at: Publisher Site | Google Scholar
  13. K. Igari, N. Sugano, T. Kudo et al., “Surgical treatment for popliteal artery entrapment syndrome,” Annals of Vascular Diseases, vol. 7, no. 1, pp. 28–33, 2014. View at: Publisher Site | Google Scholar
  14. Y. J. Kwon, T.-W. Kwon, J. G. Gwon, Y.-P. Cho, S.-J. Hwang, and K.-Y. Go, “Anatomical popliteal artery entrapment syndrome,” Annals of Surgical Treatment and Research, vol. 94, no. 5, pp. 262–269, 2018. View at: Publisher Site | Google Scholar

Copyright © 2019 Viktor Labmayr et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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