Abstract
Prolonged squatting is a well-documented cause of common peroneal neuropathy, wherein the common peroneal nerve is thought to be compressed between the biceps femoris tendon and the lateral head of the gastrocnemius muscle or the fibular head. However, deep peroneal neuropathy resulting from prolonged squatting has not been previously reported. We present the case of a tile installer who developed unilateral deep peroneal neuropathy following extended squatting, diagnosed through ultrasonography, which identified the bilateral division of the common peroneal nerves between the knee joint and the fibular head. This case underscores the value of ultrasonography, particularly when electrodiagnostic results are inconsistent with clinical expectations.
Introduction
Peripheral nerves are susceptible to entrapment within anatomical structures or compression from external pressure, leading to compressive neuropathy. Such compression may be caused by bone, bony callus, synovial thickening, ganglia, tumors, fibrous bands, or muscle (). Certain areas of the body are anatomically predisposed to compression, with the fibular head being a common site for such occurrences. Common peroneal neuropathy at the fibular head is one of the most frequent compressive neuropathies affecting the lower extremities. The common peroneal nerve wraps around the fibular head and neck, where it adheres closely to the periosteum, rendering it particularly vulnerable to compression (). This condition can lead to foot drop and tingling pain in the lower extremities, necessitating differential diagnosis from other conditions like radiculopathy (). Therefore, identifying the precise cause of neuropathy is crucial. Established causes include leg-crossing, dilated veins, drastic weight loss, schwannoma, neurofibroma, pneumatic compression, and ganglion cysts (). Prolonged squatting is also recognized as a cause of common peroneal neuropathy, where the nerve is believed to be compressed between the biceps femoris tendon and the lateral head of the gastrocnemius muscle or the fibular head (). However, deep peroneal neuropathy resulting from prolonged squatting has not been previously reported. We present the case of a tile installer who developed unilateral deep peroneal neuropathy following prolonged squatting.
Case presentation
A 27-year-old man presented with a 3-week history of right foot drop. The onset of symptoms occurred 1 week after he had spent over 8 h squatting and kneeling on his right knee while installing tiles (Figure 1). Seven days into the tile installation, he began experiencing tingling sensations in his right leg. His medical history was unremarkable, with no prior neuropathy or significant family history. He also reported no history of low back pain, and lumbar spine magnetic resonance imaging performed at another hospital was normal. Neurological examination revealed weakness in right ankle dorsiflexion, graded as 1 on the Medical Research Council (MRC) scale, and in right toe dorsiflexion, graded as 3 on the MRC scale. Sensation in the first web space of the right foot dorsum was diminished.
FIGURE 1
Nerve conduction studies and electromyography were conducted. The nerve conduction study showed normal compound muscle action potentials (CMAPs) in the right peroneal nerve when recorded from the extensor digitorum brevis (EDB) muscle and stimulated at the ankle and popliteal fossa. However, CMAPs recorded from the tibialis anterior (TA) muscle displayed reduced amplitude compared to the contralateral side. Superficial peroneal and sural sensory nerve action potentials were within the normal range. Needle electromyography revealed abnormal spontaneous activities in the right EDB and TA muscles, along with large motor unit action potentials (MUAPs) in the EDB muscle. No abnormalities were found in muscles innervated by the superficial peroneal nerve (Table 1).
TABLE 1
| Nerve | Stimulation | Right | Left | ||||
| Latency (ms) | Amplitude (mV) | CV (m/s) | Latency (ms) | Amplitude (mV) | CV (m/s) | ||
| Motor | |||||||
| Peroneal at EDB | Ankle | 3.5 | 14.5 | – | 3.3 | 16.5 | – |
| Below the fibular head | 9.9 | 13.9 | 48.4 | 9.0 | 15.6 | 54.1 | |
| Peroneal at TA | Below the fibular head | 3.0 | 3.1* | – | 3.0 | 7.3 | – |
| Above the fibular head | 4.7 | 1.0* | 58.2 | 3.9 | 5.4 | 64.0 | |
| Tibial | Ankle | 3.1 | 35.6 | 2.7 | 31.8 | ||
| Popliteal fossa | 10.8 | 30.1 | 49.9 | 10.0 | 27.1 | 50.7 | |
| Sensory | |||||||
| Superficial peroneal | Lateral leg | 3.4 | 17.9 | 3.4 | 15.0 | ||
| Sural | Calf | 3.4 | 20.9 | 3.3 | 19.4 | ||
| Muscle | IA | ASA | MUAP | Recruitment pattern | |||
| Paraspinalis (L3-S1) | Normal | None | Normal | Normal | |||
| Extensor digitorum brevis | Normal | ++ | Large | Reduced | |||
| Abductor hallucis | Normal | None | Normal | Normal | |||
| Gastrocnemius (medial) | Normal | None | Normal | Normal | |||
| Tibialis anterior | Normal | + | Normal | Reduced | |||
| Peroneus longus | Normal | None | Normal | Normal | |||
| Biceps femoris (short) | Normal | None | Normal | Normal | |||
| Vastus lateralis | Normal | None | Normal | Normal | |||
Electrodiagnostic study findings.
CV, conduction velocity; EDB, extensor digitorum brevis; TA, tibialis anterior; IA, insertional activity; ASA, abnormal spontaneous activity; MUAP, motor unit action potential.
* Indicates abnormal values in the nerve conduction study.
Given that our findings differed from the common peroneal neuropathy associated with squatting reported in the literature, we performed additional ultrasonography. Ultrasonographic evaluation revealed that, bilaterally, the common peroneal nerves divided between the knee joint and the fibular head rather than at the fibular neck. Marked swelling of the right deep peroneal nerve was observed at the fibular head level, while the left deep peroneal nerve showed no abnormal echogenicity or swelling (Figure 2). Consequently, we diagnosed the patient with right deep peroneal neuropathy and initiated rehabilitation, including range of motion exercises, strengthening exercises, and electrical stimulation therapy.
FIGURE 2
Three months later, the patient returned for a follow-up visit, during which a repeat electrodiagnostic study was performed. The CMAPs recorded from the TA muscle had improved, showing no side-to-side difference. However, abnormal spontaneous activities persisted in the right EDB and TA muscles on needle electromyography. High amplitude MUAPs and polyphasic MUAPs indicate reinnervation through collateral sprouting (). Additionally, large MUAPs were noted in the right EDB, and polyphasic MUAPs were observed in the right TA muscle, suggesting ongoing nerve regeneration. Motor strength in the right ankle and great toe had improved to MRC grade 4.
Discussion
Our report highlights a case of unilateral deep peroneal neuropathy resulting from prolonged squatting in a tile installer. The common peroneal nerve is particularly vulnerable to injury due to its superficial course at the level of the fibular head (). Consequently, positions such as sitting cross-legged and lying down are known to precipitate common peroneal neuropathy (). Squatting is also recognized as a risk factor, and several studies have documented cases of common peroneal neuropathy associated with this posture (; ; ). Based on the patient’s history and physical examination, we initially diagnosed common peroneal neuropathy due to prolonged squatting. Previous studies have reported bilateral common peroneal neuropathy following squatting (; ; ). However, given that our patient presented with unilateral symptoms, we asked him to replicate the posture he adopted while installing tiles. It became clear that only his right knee had been kneeling, explaining the unilateral presentation. Additionally, the absence of recurrent symptoms and a notable family history ruled out further evaluation for hereditary neuropathy with liability to pressure palsies.
The nerve conduction study and needle electromyography suggested injury confined to the deep peroneal nerve, while the superficial peroneal nerve remained intact. Typically, isolated injury of the deep peroneal nerve can be suspected as anterior tarsal tunnel syndrome, where entrapment occurs under the extensor retinaculum at the ankle (). However, this possibility was excluded in this patient based on electrodiagnostic studies, which revealed abnormal findings in the TA muscle. Electrodiagnostic studies are instrumental in localizing peripheral nerve lesions and predicting prognosis (). But in our nerve conduction study, the EDB muscle was only mildly affected, but the TA muscle was severely affected. Previous studies suggested that the nerve fibers to TA muscle are located most medially in the internal fascicular anatomy of peroneal nerve (). This anatomical positioning may explain why the TA muscle was severely affected. Also, the difference in conduction velocity on the affected side was not prominent. Generally, persistent compression may eventually lead to axonal loss (). Also, in compression neuropathies, various grades of peripheral nerve injury, such as neuropraxia, which can causes conduction blocks can occur (). In axonal loss lesions, conduction velocity and distal latency can be normal, provided that the largest and fastest conducting axons remain intact (). In our case, conduction velocity on the affected side was slightly decreased, suggesting that fast conducting axons were somewhat preserved. However, other axons may have experienced demyelination. Therefore, checking CMAP duration could be a useful method. Therefore, determining the lesion site was challenging. However, in our case, the conduction velocity differences on the affected side were not significant, making it challenging to precisely localize the lesion. Foot drop can also result from other conditions such as sciatic mononeuropathy, lumbosacral plexopathy, or radiculopathy (). Therefore, we employed ultrasonography as an additional diagnostic modality. A prior study found that approximately 81% of individuals exhibit bifurcation of the common peroneal nerve at or below the level of the fibular neck, with 9% bifurcating between the fibular neck and the knee joint and 10% above the knee joint line (). In our patient, we observed that the common peroneal nerve bifurcated between the knee joint and the fibular head, underscoring the value of ultrasonography as a diagnostic tool. Ultrasonography offers advantages such as being cost-effective and relatively non-invasive. Actually, we performed needle electromyography on multiple muscles in the patient, which can cause discomfort and may affect the compliance with the examination. Moreover, even if nerve conduction study results are normal, ultrasonography can provide critical diagnostic information by measuring the cross-sectional area of the nerve when symptoms are present (). In this case, we identified swelling in the affected deep peroneal nerve by comparing the cross-sectional area to the unaffected side. We also compared the diagnostic cut-off values with those reported in previous studies ().
Anatomic variations can lead to misinterpretation during electrodiagnostic studies, potentially altering the course of treatment (). Thus, accurate diagnosis is crucial, and ultrasonography, which can detect structural abnormalities or anatomical variations in real time, is a valuable complementary tool. In our case, the combination of electrodiagnostic studies and ultrasonography was particularly beneficial, especially given the anatomical variation observed.
After an accurate diagnosis using ultrasonography and electrodiagnostic studies, we prescribed range of motion exercises, strengthening exercises and electrical stimulation therapy for foot drop. Additionally, considering an ankle-foot orthosis could enhance stability during gait and help prevent falls. Also, medications such as pregabalin can be prescribed for the patient’s neuropathic pain, such as tingling sensation ().
In conclusion, when electrodiagnostic results are inconsistent with clinical expectations, ultrasonographic evaluation is necessary to identify structural abnormalities or anatomical variations in the surrounding nerves. This approach facilitates accurate diagnosis and enables more targeted treatment for the patient.
Statements
Data availability statement
The original contributions presented in this study are included in this article/supplementary material, further inquiries can be directed to the corresponding author.
Ethics statement
Ethical approval was not required for the study involving humans in accordance with the local legislation and institutional requirements. Written informed consent to participate in this study was not required from the participants or the participants’ legal guardians/next of kin in accordance with the national legislation and the institutional requirements. Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.
Author contributions
H-SJ: Investigation, Writing – original draft, Writing – review and editing. K-HK: Writing – review and editing. M-KS: Writing – review and editing. H-KP: Writing – review and editing. IC: Writing – review and editing. J-YH: Conceptualization, Investigation, Writing – review and editing.
Funding
The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This study was financially supported by the Chonnam National University (grant number: 2023-0890-01).
Acknowledgments
We would like to thank the patient and the patient’s family for their trust in us.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
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Summary
Keywords
peroneal nerve, neuropathy, anatomic variation, nerve compression syndromes, ultrasonography
Citation
Jo H-S, Kim K-H, Song M-K, Park H-K, Choi IS and Han J-Y (2024) Deep peroneal neuropathy induced by prolonged squatting: a case report. Front. Neuroanat. 18:1474791. doi: 10.3389/fnana.2024.1474791
Received
02 August 2024
Accepted
30 September 2024
Published
09 October 2024
Volume
18 - 2024
Edited by
Nicola Montemurro, Azienda Ospedaliera Universitaria Pisana, Italy
Reviewed by
Edvard Ehler, Eldis Pardubice, Czechia
Hassan Aboumerhi, University Hospitals of Cleveland, United States
Updates
Copyright
© 2024 Jo, Kim, Song, Park, Choi and Han.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Jae-Young Han, rmhanjy@daum.net
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.