|Year : 2017 | Volume
| Issue : 4 | Page : 147-152
Medial calcaneal neuropathy: a missed etiology of chronic plantar heel pain
Emmanuel Kamal Aziz Saba, Sarah Sayed El-Tawab, Hussein Al-Moghazy Sultan
Department of Physical Medicine, Rheumatology and Rehabilitation, Faculty of Medicine, Alexandria University, Alexandria, Egypt
|Date of Submission||23-Mar-2017|
|Date of Acceptance||27-Jul-2017|
|Date of Web Publication||31-Oct-2017|
Emmanuel Kamal Aziz Saba
Department of Physical Medicine, Rheumatology and Rehabilitation, Faculty of Medicine, Alexandria University, Alexandria, 21131
Source of Support: None, Conflict of Interest: None
Introduction Medial calcaneal neuropathy had been implicated as a source of chronic plantar heel pain.
Aim The aim was to determine the presence of medial calcaneal neuropathy as a cause of chronic plantar heel pain.
Patients and methods The present study included 43 heels obtained from 38 patients with chronic plantar heel pain and 30 apparently healthy volunteers as a control group. Clinical examination was done. Sensory nerve conduction study of the medial calcaneal nerve was performed. This was a single-center, public hospital-based study. It was designed as a cross-sectional examination of consecutive patients with chronic plantar heel pain.
Results There were 27 (62.79%) heels, from 23 (60.52%) patients, who had medial calcaneal neuropathy. From them, unobtainable medial calcaneal nerve response was present in 10 (37.03%) heels of nine (39.13%) patients. Medial calcaneal neuropathy was the solitary cause of chronic plantar heel pain in 10 (37.03%) heels from 10 (43.48%) patients. However, it was associated with other local heel pathologies in the remaining patients. The majority of them were having plantar fasciitis in nine (33.34%) heels from five (21.73%) patients.
Conclusion Medial calcaneal neuropathy is present in a considerable number of patients with chronic plantar heel pain. It should be taken into consideration during the assessment of any patient with chronic plantar heel pain.
Keywords: chronic heel pain, medial calcaneal nerve, medial calcaneal neuropathy, plantar heel pain, tarsal tunnel syndrome
|How to cite this article:|
Saba EA, El-Tawab SS, Sultan HA. Medial calcaneal neuropathy: a missed etiology of chronic plantar heel pain. Egypt Rheumatol Rehabil 2017;44:147-52
|How to cite this URL:|
Saba EA, El-Tawab SS, Sultan HA. Medial calcaneal neuropathy: a missed etiology of chronic plantar heel pain. Egypt Rheumatol Rehabil [serial online] 2017 [cited 2018 May 25];44:147-52. Available from: http://www.err.eg.net/text.asp?2017/44/4/147/217436
| Introduction|| |
Plantar heel pain is a commonly encountered problem that causes significant discomfort. Several causes have been implicated to cause chronic plantar heel pain ,. The neurological etiologies of it include entrapment neuropathy of medial plantar nerve, lateral plantar nerve, or medial calcaneal nerve (MCN) branches of the posterior tibial nerve . Medial calcaneal neuropathy is considered to be a form of tarsal tunnel syndrome (TTS), when it occurs solitary and is not associated with medial or lateral plantar neuropathies ,,.
Medial calcaneal nerve is a sensory nerve. It is the first branch that arises from the posterior tibial nerve at the level of the ankle ,,,. The MCN provides sensory innervation to the inferior, medial, and posterior aspects of the heel and the calcaneus .
Medial calcaneal neuropathy is considered to be the second most common reported neuropathy that causes plantar heel pain of neural origin ,,,. It is usually missed in the differential diagnosis of plantar heel pain, especially the chronic ones ,,,,. The diagnosis of it could be difficult because its symptoms are often subjective and are mimicking those associated with other heel and foot pathological conditions ,. There are scanty studies that assessed this issue.
The aim of this study was to determine the presence of medial calcaneal neuropathy as a cause of chronic plantar heel pain.
| Patients and methods|| |
The present study included 43 heels obtained from 38 patients with chronic plantar heel pain from those attending the outpatient clinic of Physical Medicine, Rheumatology and Rehabilitation Department, Main University Hospital, Alexandria Faculty of Medicine, and 30 apparently healthy volunteers (30 heels) as a control group. The volunteers included medical staff, their relatives and patients’ relatives. Plantar heel pain of at least 3 months duration was considered to be chronic . Exclusion criteria included diabetes mellitus, endocrine disorders, metabolic disorders, and neurological disorders including lumbosacral radiculopathy, peripheral neuropathy, and TTS affecting the medial and/or lateral plantar nerves. The study was explained to the participants and an informed consent was given by each. The study had been approved by the ethics committee of the Faculty of Medicine, Alexandria University, Egypt.
Demographic data collection and history taking were done stressing on the presence of subjective burning pain and/or paresthesia or numbness over the territory of MCN. Clinical examination was done stressing on the musculoskeletal and neurological examination of the lower limb. Assessment of sensation over the territory of the MCN was done to detect the presence of objective sensory loss in the form of hypoesthesia or anesthesia ,,.
Electrophysiological studies were conducted on a Nihon Kohden Neuropack MEB-7102 mobile unit with a two-channel evoked potential/electromyography measuring system (Nihon Kohden Corporation, Tokyo, Japan). Skin temperature at the site of the recording electrodes was maintained around 32–34°C by means of an infrared lamp. The skin of the stimulation and recording sites were abraded with a commercial cleansing stone especially the heel and cleansed with alcohol. The ground electrode was placed between the recording electrodes distally and the stimulation site proximally. Conduction distances were measured by a measuring tape with a precision of 1 mm .
Sensory nerve conduction study of the MCN was done by using an antidromic technique. It was done for patients and for the apparently healthy volunteers (control group). The following was applied: the sweep speed was 2 ms/division and the sensitivity was 5–10 μV/division. The filter bandwidth was 20 Hz–2 kHz. The bipolar stimulator had a production current ability of 50 mA. The pulse duration was 0.2 ms. Signal averaging was applied. Responses were superimposed to ensure reproducibility. Supramaximal stimulation was ensured. Measurements of the sensory nerve action potential (SNAP) included onset latency (in milliseconds), peak latency (PL) (in milliseconds), amplitude (in microvolts), and conduction velocity (CV) (meter per second) using onset latency .
The antidromic technique for doing the sensory nerve conduction study of the MCN was as follows: the active recording surface disc electrode was placed in a point at one-third the distance between the apex of the heel to a point midway between the navicular tuberosity and the prominence of the medial malleolus. The reference surface disc electrode was placed on the apex of the heel. Electrical stimulation was done at about 2 cm posterior to the medial edge of the tibia, at about 10 cm proximal to the active recording electrode . [Figure 1] is an illustration of the technique of MCN sensory nerve conduction study.
|Figure 1 This is an illustration for the stimulation technique and recording electrodes position for the medial calcaneal nerve sensory conduction study.|
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The diagnosis of medial calcaneal neuropathy depended on the presence of subjective burning and tingling sensation or objective sensory loss in the territory of the MCN with or without the presence of positive Tinel’s sign in an area inferior and posterior to the medial malleolus. This was confirmed with the results of the sensory conduction study of the MCN ,. Patients with medial calcaneal neuropathy were considered group I, whereas group II included patients without medial calcaneal neuropathy.
Statistical analysis of data was done using the statistical package for the social sciences (SPSS version 17) software . Descriptive measures [count, frequency, minimum, maximum, mean, and standard deviation (SD)] as well as analytic measures (Mann–Whitney test, Kruskal–Wallis test, and Pearson’s Chi-square-test) were used. Correlation study was done using Spearman’s correlation test. Statistical significance was assigned to any P value at less than 0.05. The reference cutoff values of the electrophysiological studies were calculated by rounding the mean plus or minus two SD to measure the upper limit of normal or the lower limit of normal, respectively.
| Results|| |
The present study included 43 heels obtained from 38 patients with chronic plantar heel pain [26 (68.42%) women]. Their mean age was 40.67±9.91 years (range: 21–62 years). The control group consisted of 30 asymptomatic heels that were obtained from 30 apparently healthy individuals [20 (66.67%) women]. Their mean age was 39.00±11.58 years (range: 19–60 years). There were no statistically significant differences between patients and control group as regards sex (χ2=0.024, P=0.878) and age (Z=−0.404, P=0.686). The clinical characteristics of the patients and controls are summarized in [Table 1].
Reference values for different parameters of the MCN SNAP from the controls are shown in [Table 2].
|Table 2 The determined reference cutoff values of medial calcaneal nerve sensory conduction study parameters obtained from the control group|
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The patients were subdivided into two groups according to the presence of medial calcaneal neuropathy. Group I included patients with medial calcaneal neuropathy, whereas group II included patients without medial calcaneal neuropathy. There were 27 (62.79%) heels obtained from 23 (60.52%) patients who had medial calcaneal neuropathy (group I) proved clinically and electrophysiologically. From them, unobtainable medial calcaneal nerve response was present in 10 (37.03%) heels of nine (39.13%) patients. The comparison between the two patient groups and the control group as regards the results of the nerve conduction study of the MCN are shown in [Table 3].
|Table 3 Comparison of the clinical characteristics and different medial calcaneal nerve sensory conduction study parameters between the two patient groups and the control group|
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There were statistically significant differences between parameters of MCN SNAP among the two patient groups and control group as regards the PL, CV, and amplitude of MCN SNAP, as well as, among the two patient groups, and among group I (patients with medial calcaneal neuropathy) and control group. Regarding the disease duration of chronic plantar heel pain, it was significantly longer among group I patients when compared with group II patients ([Table 3]).
There was a statistical significant negative correlation between the MCN SNAP amplitude and duration of complaints (r=−0.435, P=0.013). Otherwise, there was no statistically significant correlation between the MCN SNAP parameters and age (P>0.05).
[Table 4] illustrates the different final diagnosis of all patients in the study. Among the patient group with medial calcaneal neuropathy (group I), medial calcaneal neuropathy was the solitary cause of chronic plantar heel pain in 10 (37.03%) heels obtained from 10 (43.48%) patients. However, it was associated with other local heel pathologies in the remaining patients. The majority of them were plantar fasciitis in nine (33.34%) heels from five (21.73%) patients.
|Table 4 Diagnosis of patients with chronic plantar heel pain in the two patient groups|
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| Discussion|| |
A potential etiology for chronic plantar heel pain is entrapment of MCN under the flexor retinaculum or compressed behind the medial malleolus ,,. However, it is a frequently under-recognized cause of heel pain. The medial calcaneal neuropathy produces symptoms that are frequently subjective because it is a pure sensory nerve. Subsequently, it is usually missed. It was postulated that the entrapment of the MCN is a rare condition .
In the current study, medial calcaneal neuropathy was detected in 27 (62.79%) heels obtained from 23 (60.52%) patients. It was the solitary diagnosis for chronic plantar heel pain in 10 (37.03%) patients. Its high prevalence is an indicator of a considerable health problem. Unfortunately, it is usually missed in patients with chronic plantar heel pain. This condition is usually overlooked because the more obvious local musculoskeletal disorders and injuries draw the physician’s attention. This could be due to the similarity of its symptoms with other causes of plantar heel pain. Its clinical signs are usually missed and unreliable. In addition, the electrophysiological assessment of MCN is not used routinely .
It was reported that MCN is affected in about two-thirds of TTS patients. This is because it arises proximal to the tarsal tunnel and descends superficial to the flexor retinaulum . However, it was postulated that isolated medial calcaneal neuropathy is rare . A study reported 11 heels from 10 patients with chronic heel pain secondary to entrapment of the MCN. Surgical decompression was done with improvement in 10 (90.9%) heels . Another study reported one (4%) patient with solitary medial calcaneal neuropathy among 25 patients with TTS . The present study is not in agreement with this study due to differences in the studied patients. Patients with TTS affecting the medial and/or lateral plantar nerves were excluded in the current study. Seo et al.  reported four cases with only medial calcaneal neuropathy as an illustration for the efficacy of an electrophysiological technique for assessment of MCN. Cheong et al.  presented a single case report of medial calcaneal neuropathy as a cause of intractable heel pain.
In the current study, the duration of chronic plantar heel pain was significantly longer among the patient group with medial calcaneal neuropathy. This could be due to the delay in the diagnosis of medial calcaneal neuropathy. Making the patient receive inappropriate medical therapy which is not effective or has only a placebo effect with slight improvement of the condition then recurrence after stopping the therapy .
There are many etiologies that lead to medial calcaneal neuropathy. These include compression of the nerve by hypertrophic flexor retinaculum, tendonopathy, any space occupying lesions as ganglion, lipoma, neuroma, and lower limb varicosities ,. Moreover, these include foot deformity as hind foot valgus deformity, prolonged weight bearing periods as walking and standing, lower limb edema of any cause, obesity, post surgical scarring and inflammatory arthropathies as rheumatoid arthritis ,. It may be caused by chronic microtrauma associated with repetitive biomechanical overload. The heel fat pad acts as a natural shock absorber for the body. This is deficient in case of heel pad syndrome due to atrophy of heel fat pad. Because the branches of the MCN usually lie superficial to the intrinsic foot muscles and plantar fascia, subsequently, they are likely to be traumatized and irritated following heel fat pad atrophy ,. Repetitive trauma to the heel can lead to extraneural, as well as, intraneural fibrosis involving the MCN . It could be affected by direct trauma to the heel which lead to contusion and the bleeding is healed by adhesions and perineural fibrosis .
In the present study, medial calcaneal neuropathy was associated with plantar fasciitis in nine (33.34%) heels. The current study is in agreement with Rose et al.  and Chang et al. . Rose et al.  reported that solitary medial calcaneal neuropathy was associated with plantar fasciitis in 22.68% of their patients, whereas 49.48% of their patients had medial calcaneal neuropathy in association with medial plantar neuropathy . Chang et al.  reported that medial calcaneal neuropathy was associated with plantar fasciitis in six (23.1%) patients with unilateral plantar fasciitis. This could be because the etiology of both conditions; i.e. medial calcaneal neuropathy and plantar fasciitis; could be the same which is excessive load that could be the result of prolonged standing and walking with excessive activity .
The current study is in agreement with Park and Toro , who assessed sensory nerve conduction study of the MCN by using an antidromic technique, regarding PL and amplitude of the MCN SNAP. However, it does not agree with them regarding the SNAP CV which was much slower in the current study. This could be due to differences in the study population. Park and Toro  studied participants who were younger than the control group of the current study (mean age: 30 years; range: 22–45 years).
Chang et al.  estimated the lowest normal MCN CV to be 34.3 m/s and the lowest normal SNAP amplitude to be 6.1 μV. The current study is in agreement with Chang et al.  regarding the lowest normal MCN CV. However, it is not in agreement with them regarding the SNAP amplitude. This could be due to difference in the study population who were older than those of the current study (mean age: 50.3±5.3 years), as well as, the difference in the techniques of MCN recording between the two studies .
The current study had few limitations. First, the relatively larger number of female patients included in the current study. This could be because men seek medical advice only in late stages of their illness; they are usually seeking medical advice in the health insurance services related to their employment; and also they are working in the morning and tend to seek medical advice in the private clinics in the evening and at night. Second, the current study was conducted in the Physical Medicine, Rheumatology and Rehabilitation outpatient clinic and did not include other clinics where patients with chronic plantar heel pain could attend as Orthopedic Surgery outpatient clinic and Internal Medicine (Rheumatology subunit) outpatient clinic.
In conclusion, medial calcaneal neuropathy is present in a considerable number of patients with chronic plantar heel pain. It should be taken into consideration during the assessment of any patient with chronic plantar heel pain.
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Conflicts of interest
There are no conflicts of interest.
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[Table 1], [Table 2], [Table 3], [Table 4]