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"Fos"

Case Report

Neurovascular Compression Caused by Popliteus Muscle Enlargement Without Discrete Trauma
Kyoung Jin Cho, Sangkuk Kang, Sanghyung Ko, Junghyun Baek, Yeongkyun Kim, Noh Kyoung Park
Ann Rehabil Med 2016;40(3):545-550.   Published online June 29, 2016
DOI: https://doi.org/10.5535/arm.2016.40.3.545

Popliteal entrapment syndrome caused by isolated popliteus muscle enlargement is very rare, although its occurrence has been reported after discrete trauma. However, popliteal artery stenosis with combined peroneal and proximal tibial neuropathy caused by popliteus muscle enlargement without preceding trauma has not been reported. A 57-year-old man presented with a tingling sensation and pain in his left calf. He had no previous history of an injury. The symptoms were similar to those of lumbosacral radiculopathy. Calf pain became worse despite treatment, and the inability to flex his toes progressed. Computed tomography angiography and magnetic resonance imaging of the lower extremity showed popliteal artery stenosis caused by popliteus muscle enlargement and surrounding edema. An electrodiagnostic study confirmed combined peroneal and proximal tibial neuropathy at the popliteal fossa. Urgent surgical decompression was performed because of the progressive neurologic deficit and increasing neuropathic pain. The calf pain disappeared immediately after surgery, and he was discharged after the neurologic functions improved.

Citations

Citations to this article as recorded by  
  • Layer-Specific Architecture and Nerve Innervation of the Popliteus Muscle: Neuroanatomical Basis for Precision-Guided Interventions for the Knee Joint
    Soo-Jung Kim, Ji-Hyun Lee, In-Seung Yeo
    Diagnostics.2026; 16(6): 834.     CrossRef
  • Uncommon complication in traumatic ACL rupture: Tibial neuropathy due to popliteus muscle haemorrhage: A case report
    Maarten Rombauts, Arne Hautekiet, Koen Matthys, Willem Goethals
    Journal of Orthopaedic Reports.2025; 4(1): 100351.     CrossRef
  • Tibial Nerve Palsy Secondary to Spontaneous Isolated Popliteus Muscle Rupture and Localized Compartment Syndrome
    Sophie Jolliet, Yves Harder, Sébastien Durand
    Diagnostics.2025; 15(23): 2990.     CrossRef
  • Diagnostic Approach to Lower Limb Entrapment Neuropathies: A Narrative Literature Review
    Nicu Cătălin Drăghici, Vitalie Văcăraș, Roxana Bolchis, Atamyrat Bashimov, Diana Maria Domnița, Silvina Iluț, Livia Livinț Popa, Tudor Dimitrie Lupescu, Dafin Fior Mureșanu
    Diagnostics.2023; 13(21): 3385.     CrossRef
  • Nerve and Arterial Supply Pattern of the Popliteus Muscle and Clinical Implications
    Anna Jeon, Ye-Gyung Kim, Youngjoo Sohn, Je-Hun Lee, Friedrich P. Paulsen
    BioMed Research International.2022;[Epub]     CrossRef
  • Macroscopic observations of muscular bundles of accessory iliopsoas muscle as the cause of femoral nerve compression
    Fuat Unat, Suzan Sirinturk, Pınar Cagimni, Yelda Pinar, Figen Govsa, Gkionoul Nteli Chatzioglou
    Journal of Orthopaedics.2019; 16(1): 64.     CrossRef
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Original Articles
The Effect on Fos Expression in Rat Spinal Cord following Stimulation to Dorsal Root Ganglion by Pulsed Radiofrequency.
Seo, Jeong Hwan , Byeon, Whan Taek , Kwon, Young Bae , Sim, Young Joo
J Korean Acad Rehabil Med 2007;31(4):387-393.
Objective
To reconfirm the relationship between the Fos expression and the pulsed radiofrequency which very few articles have reported. Method: Thirty-four male Sprague-Dawely rats were enrolled: 8 for lumbar 3rd dorsal root ganglion (DRG) stimulation, 4 for L3 and L4 DRGs, 5 for C5 and C6 DRGs, 8 for sham L3 DRGs, 5 for sham L3 and L4 DRGs, and 4 for sham C5 and C6 DRGs. Without laminectomy, each lumbar DRG was stimulated with PRF for 2 minutes 2 times with 42°C. Sham group was stimulated with PRF electrode but without any stimulation. Three hours after the stimulations, spinal cord was thin sectioned for immunohistochemistry and Fos expression was calculated. Individual sections were digitized with 4096 gray levels using a computer assisted image analysis system. With laminectomy, cervical DRGs was stimulated with the same method of lumbar DRGs. Sham stimulation was applied to the sham group. Results: No significant difference of Fos expression was observed on dorsal horn of rat in operated site, 3 hours later after operation, between the PRF and sham group in lumbar DRGs and the PRF and sham groups in cervical DRGs. Conclusion: The expression of Fos was not significantly related with the cervical and the lumbar DRGs stimulation with PRF. (J Korean Acad Rehab Med 2007; 31: 387-393)
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The Cross Effects of Needle Electrical Stimulation according to Electrode Placements on the Analgesia in Arthritic Rat Model.
Kim, Kyoung Yoon , Kim, Gye Yeop , Jung, Sung Hwan , Kim, Jae Hyung , Lee, Sam Gyu
J Korean Acad Rehabil Med 2007;31(2):143-149.
Objective
To investigate the analgesic effect of needle electrical stimulation (NES) according to the electrode placement in acute arthritic rat model. Method: Male Sprague-Dawley rats (120 rats, 250⁑50 g) were injected with a mixture of 3% carrageenan and 3% kaolin into the right knee joint. Rats were randomly assigned into one of four groups: Group I, control group (n=30); Group II, arthritic limb-induced control group (n=30); Group III, NES application group on the ipsilateral arthritic limb (n=30); Group IV, NES application group on the contralateral arthritic limb (n=30). We applied the NES (2 Hz, 200μs, 20 min) to group III and IV. We assessed the change of paw withdrawal latency (PWL) and the immunoreactivity of c-fos by immunohistochemistry at baseline, 4, 8, 12 and 24 hours after induction of arthritis. Results: NES was more effective in Group III and IV than group II 8 hours after the induction of arthritis (p<0.001) based on the results of PWLs and c-fos immunoreactivity. The analgesic effects of Group III were greater than those of group IV (p<0.001). Conclusion: Contralateral NES on arthritic limb reduced pain in arthritic rat model as effectively as ipsilateral NES. (J Korean Acad Rehab Med 2007; 31: 143-149)
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Mechanism of Electrical Stimulation on Functional Recovery Following Spinal Injury in Rats.
Lee, Jae Sung , Lee, Moon Young , Kim, Min Sun , Park, Dong Sik , Choi, Suck Jun , Park, Byung Rim
J Korean Acad Rehabil Med 1997;21(2):281-289.

The present study was designed to investigate the effects and action mechanism of electrical stimulation on functional recovery following spinal cord injury in Sprague-Dawley rats. Electrical stimulation with 0.2 ms, 20 Hz, 1-3 V was applied to the sciatic nerve for 4 hours/day during 6 days following dorsal hemisection of the T10 spinal cord. After 7 days of spinal cord injury, mechanical properties of muscle contraction including contraction time, half relaxation time, maximum twitch tension, maximum tetanic tension, and fatigue index were measured in the soleus and medial gastrocnemius muscles, and the number of c-fos immunoreactive cells was counted in the upper lumbar cord. In mechanical properties of muscle contraction of normal rats, contraction time and half relaxation time of the soleus muscle were 1.5 times and 2 times as long as those of the medial gastrocnemius muscle, respectively. And fatigue index of the soleus muscle was 0.19⁑0.4 and the medial gastrocnemius muscle was 0.82⁑0.03. According to the above characteristics, the soleus muscle was mainly composed of slow muscle fibers and the medial gastrocnemius muscle was composed of fast muscle fibers. Maximum twitch tension, maximum tetanic tension, and fatigue index of both muscles following spinal cord injury were decreased significantly compared to the control group (p<0.01). In electrically stimulated rats following spinal cord injury, maximum twitch tension, maximum tetanic tension, and fatigue index were significantly increased compared to spinal cord injured rats. The number of c-Fos immunoreactive cells was increased markedly at the upper lumbar cord in electrically stimulated rats.

These results may suggest that electrical stimulation not only prevents from muscle atrophy in slow and fast muscles through efferent nerve fibers, but also promotes functional plasticity through afferent nerve fibers by activating silent synapse and regulation of receptors for neurotransmitters.

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