Peripheral nerve ultrasound (US) has emerged as a promising technique for the diagnosis of peripheral nerve disorders. While most experience with US has been reported in the context of nerve entrapment syndromes, the role of US in the diagnosis of peripheral neuropathy (PN) has recently been explored. Distinctive US findings have been reported in patients with hereditary, immune-mediated, infectious and axonal PN; US may add complementary information to neurophysiological studies in the diagnostic work-up of PN. This review describes the characteristic US findings in PN reported to date and a classification of abnormal nerve US patterns in PN is proposed. Closer scrutiny of nerve abnormalities beyond assessment of nerve calibre may allow for more accurate diagnostic classification of PN, as well as contribute to the understanding of the intersection of structure and function in PN.
- GUILLAIN-BARRE SYNDROME
- HMSN (CHARCOT-MARIE-TOOTH)
- DIABETIC NEUROPATHY
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Peripheral neuropathy (PN) contributes significantly to the neurological burden of disease worldwide.1 ,2 Prevalence of PN is increasing, particularly when associated with the growing population affected by diabetes,3 and the rising incidence of drug-induced neuropathy associated with chemotherapy and antiretroviral drugs.4 ,5
Traditionally, the diagnostic work-up of PN involves delineating a pattern of clinical involvement through history and examination, with the diagnosis confirmed by neurophysiological studies. In some situations, the clinical features and associated comorbidities may be enough to diagnose PN without further investigations,6 although grading of severity and monitoring of progression often includes neurophysiological assessment. However, the diagnosis of PN by clinical and neurophysiological grounds alone may be difficult, particularly in those patients with atypical or proximal demyelinating PN.7 It may also be difficult to distinguish acquired from inherited demyelinating PN.8 Hence, there is a need to develop novel strategies to aid in the diagnosis and monitoring of patients with PN, in particular the demyelinating forms.
The peripheral nervous system was unavailable to imaging modalities prior to the 1990s because of insufficient resolution and poor discrimination of nerves from surrounding soft tissues. However, recent technical developments have allowed imaging techniques, including MR neurography (MRN) and ultrasound (US), to play an important role in the diagnostic algorithm of peripheral nerve disorders. MRN currently provides an excellent depiction of three-dimensional nerve anatomy and pathology, and development of diffusion tensor imaging and tractography may provide further functional data.9 ,10 US provides superior spatial resolution that has enabled detailed visualisation of even the smallest peripheral nerves. Evolution of high-frequency broadband transducers (up to 22 MHz), advances in image postprocessing and sensitive Doppler technology, that allows assessment of nerve vascularity without contrast administration, have improved the ability of US to detect anatomic details and subtle structural abnormalities in peripheral nerves. In addition, the acquisition of US is a real-time dynamic process and allows the examiner to explore the entire course of the nerve in a single sweep. Finally, US has the general advantages of being a painless, non-invasive and inexpensive technique. As such, US may be considered to be an optimal tool to look for structural nerve pathology, and hence serve as a complementary technique to clinical and neurophysiological diagnosis of patients with PN. This review will discuss the US features of PN, focusing on situations in which US studies may make a positive contribution to the diagnosis.
US features of normal peripheral nerve
The US features of peripheral nerves correspond to macroscopic and microscopic anatomy.11 Peripheral nerves are visualised on US as tubular structures with a characteristic fascicular appearance (figures 1 and 2). On longitudinal images, linear hypoechoic fascicles are seen, separated by bands of hyperechoic perineurial connective tissue. On axial images, the peripheral nerves demonstrate a ‘honeycomb’ appearance, with ovoid hypoechoic fascicles embedded in a hyperechoic background. The dense epineurial connective tissue surrounding the nerve is highly reflective of sound waves, which results in a hyperechoic rim that may provide a means of demarcating the nerve from surrounding structures.
There are some situations where the US appearance of normal nerves differs from a typical fascicular pattern. Nerves are more hypoechoic and demonstrate fewer or no fascicles in very proximal nerves, such as the brachial plexus and cervical nerve roots,12 because of reduced volume of connective tissue and more tightly packed fascicles.13 Echogenicity and fascicle number may also be reduced where they cross osteofibrous tunnels, such as the ulnar nerve in the cubital tunnel.14 The size of peripheral nerves decreases slightly proximal to distal in the limb and it may be greater in entrapment sites in normal individuals.14 ,15
Commercially available US units are able to assess most peripheral nerves of the upper limbs, lower limbs and brachial plexus. However, very deep nerves such as the proximal sciatic nerve may be difficult to image, and the lumbar and sacral plexus cannot be visualised using US.
US features of injured peripheral nerve
US findings following peripheral nerve injury converge on a number of common features. These changes include alterations in nerve size, nerve echotexture, definition of the epineurial margins, fascicle diameter and vascularity. Much of the literature describing peripheral nerve changes following nerve injury is based on assessment of entrapment neuropathies.16 In nerve compression, there may be focal nerve enlargement, loss of the internal fascicular appearance and decrease in nerve echogenicity.17
Nerve enlargement is most commonly quantified using cross-sectional area (CSA) traced within the hyperechoic epineurial rim. CSA is a reliable measure with a good intraobserver and interobserver agreement and reproducibility;18 therefore, it has been most frequently used to quantify changes in neuropathy and reference values have been established for the major limb nerves in several anatomic locations and for the brachial plexus.15 ,19–21 It is worthwhile noting that some studies have demonstrated that nerve size may be influenced by age, gender, body mass index and height.15 ,19 Temperature of the limb may also influence nerve calibre.22 As such, it is recommended that comparison groups in studies of nerve US are matched for those subject characteristics and standardised environmental conditions are employed during the study.
Measuring the size of individual nerve fascicles may also contribute important pathophysiological information for the nerve injury and PN, although presently there is very little published data.23 Fascicle size can differ between individuals, nerves and anatomic regions of an individual nerve, and hence a standardised approach would be required to systematically study this.
Peripheral nerve echogenicity may be quantified by measuring the mean grey scale value of the nerve image. Alternatively, thresholding techniques may be applied to determine the proportion of the nerve that is relatively hypoechoic.14 ,24 ,25 Data obtained using each of these approaches is specific to the US system being used and cannot be compared with data from another site unless the values are calibrated using a universal phantom.
Nerve vascularity, as measured by Doppler, may also provide insights into the pathophysiology of peripheral nerve disease. In normal nerves there is no detectable blood flow.26 Increased blood flow may be detected in compressive mononeuropathy and inflammatory PN,16 ,27 possibly reflecting vascular proliferation precipitated by chronic trauma or inflammation (figure 3).
US findings in PN
US is emerging as a valuable tool in the diagnosis of PN and it is in this field where it is anticipated that US will have a significant impact in rationalising the diagnostic pathway, potentially reducing the number of expensive investigations performed and focusing the use of expensive immunomodulatory therapies.28 In this section, the US findings documented to date in hereditary, immune-mediated, infectious and axonal neuropathies will be discussed.
Charcot-Marie-Tooth disease (CMT) is a clinically and genetically heterogeneous hereditary neuropathy characterised by distal muscle atrophy, weakness and sensory loss with reduced tendon reflexes. More than 60 different causative gene mutations have been described.29 Nerve conduction studies still remain crucial both for the diagnosis and the classification of CMT (demyelinating type or axonal type), whereas US has emerged as a convenient technique to assess morphological changes of peripheral nerves in patients with CMT as a complement to the neurophysiological evaluation.
Nerve US findings of patients with CMT were first described in 1999 by Heinemeyer and Reimers 30 They examined nerve diameter, but not CSA, in patients with CMT. They concluded that nerve diameter and echogenicity did not differ significantly between patients with CMT and healthy subjects, and noted that the visualisation of nerves with the 7.5 MHz linear array probe was often difficult because of increased echogenicity of adjacent muscles in patients with CMT. The negative findings of this study may be explained by the limitations of resolution and recent studies using higher frequency probes (≥12 MHz) have provided further information regarding nerve morphology in patients with various subtypes of CMT.
CMT disease type 1A
CMT1A, the most common form of demyelinating CMT, is caused by a duplication of PMP22 that encodes peripheral myelin protein 22, a transmembrane protein in the compact myelin of the peripheral nerves. Schwann cells and abundant connective tissue around thinly myelinated axons (‘onion bulbs’) are the main features of pathology in CMT1A. In patients with CMT1A, nerve US reveals that the CSA of peripheral nerves, brachial plexus and nerve roots are larger than those in healthy subjects. Nerve CSA is uniformly increased throughout the course of the nerve, and the CSA and diameter of the C6 nerve root are also larger than those in controls (figure 1). Martinoli et al31 reported that patients with CMT1A can be distinguished from those with other types of CMT (CMT2 and CMTX1) by either a larger CSA or a larger fascicular diameter in median nerves. Likewise, Noto et al32 demonstrated that CSA was also increased in the great auricular nerves and in C6 nerve roots in patients with CMT1A. Thus, nerve US findings demonstrate why CMT1A was previously classified as a hypertrophic neuropathy based just on nerve palpation.
Regarding the CSAs of the sural nerves, two conflicting descriptions have been reported. Pazzaglia et al33 found that the CSA in the sural nerve was not increased in the majority of patients with CMT1A. Noto et al32 found that the CSA in the sural nerve was increased in their population with CMT1A. One possible reason for this discrepancy can be attributed to the different methods of CSA measurement between their studies. Pazzaglia et al tracked the nerve circumference inside the hyperechoic rim, whereas Noto et al traced the nerve circumference including hyperechoic rim.
In terms of the correlation between US, clinical and electrophysiological findings in CMT1A, there is an inverse relationship between the CSA and the nerve conduction parameters, such as motor conduction velocity and compound muscle action potentials amplitude.23 ,32 There is also a positive correlation between the CSAs in the median nerve and CMT neuropathy score (CMTNS) that quantifies the disease severity in patients with CMT1A.32 Taken together, in patients with CMT1A, the extent of nerve enlargement assessed by US paralleled not only the physiological function of peripheral nerves but also the clinical disease severity.
CMT disease type 1B
CMT1B, another demyelinating form of CMT, is caused by mutations of MPZ gene that encodes myelin protein zero, a major constituent of peripheral myelin proteins. In a study involving a large family with CMT1B, enlargement of the median and vagus nerves was detected in affected family members.34 Conversely, sural nerve calibre was reduced, possibly reflecting length-dependent axonal loss.
CMT disease type 2
CMT2, a group of axonal forms of autosomal dominant CMT, includes more than 19 distinct types. Among them, the most common form is CMT2A that is caused by mutations of mitofusin 2 (MFN2) gene. In axonal neuropathies, axonal loss is predicted to result in decreased nerve caliber; however, median nerve CSA in patients with CMT2 is slightly larger than that of normal subjects.23 ,31 This discrepancy may be related to histopathological findings that include Schwann cell hyperplasia with pseudo onion bulb formations and endoneurial swelling seen in some genetic subtypes of CMT2.35
CMT disease type X1
CMTX1, the second most common form of CMT, is caused by point mutations of gap junction-associated protein B1 (GJB1) gene, which encodes connexin-32 protein. Although a statistically significant difference was not demonstrated, the median nerve CSAs in patients with CMTX1 were larger than those in healthy subjects in one study, but were smaller in another report.23 ,31 Both studies included a small number of patients; therefore, a further study with larger number of patients will be needed.
With the accumulation of future studies of US findings in various types of CMT, nerve US in combination with results of nerve conduction studies may provide tools to facilitate more targeted gene analysis in patients with suspected CMT. Nerve US is also useful for the diagnosis of hypertrophic-type CMT in the rare instance when compound muscle action potentials are not evoked in demyelinating CMT due to severe atrophy in distal muscles or marked increase in stimulation threshold.
Hereditary neuropathy with liability to pressure palsies
Hereditary Neuropathy with liability to pressure palsies (HNPP) is caused by a deletion of PMP22 and nerve biopsies in such patients reveal focal thickening of myelin, that is, tomacula. Beekman and Visser36 first reported focal and multiple nerve enlargements in a patient with HNPP not only at typical nerve entrapment sites but also outside the entrapment sites. Non-uniform nerve enlargement patterns have been reported in some studies of patients with HNPP.23 ,37 ,38 Gianneschi et al37 revealed that no morphometric changes were seen in the distal nerve segments where entrapment is unlikely while the distal motor latencies were increased. Morphological abnormalities identified on US were not always correlated to the neurophysiological parameters in patients with HNPP, unlike those in patients with CMT1A.
Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP)
The clinical features of typical chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) are well recognised, including progressive symmetric weakness involving proximal more than the distal muscles, sensory impairment and reduced or absent deep tendon reflexes. Histopathologically, nerves in patients with CIDP demonstrate segmental demyelination and remyelination resulting in onion bulb formation and varying degrees of interstitial oedema and endoneurial inflammation.39 There are also a number of atypical or variant presentations, such as multifocal acquired demyelinating sensory and motor neuropathy (MADSAM), sensory-predominant CIDP, and distal forms such as distal acquired demyelinating sensory neuropathy (DADS).40–42
In the majority of patients with CIDP, abnormalities are detected on nerve US. However, just as there is clinical variability, there is a wide range of nerve US findings reported in CIDP (figure 3). Increased CSA of peripheral nerves and/or cervical nerve roots is most frequently reported.43–48 Hypertrophy of the vagus nerve has also been reported in CIDP.49 ,50
While nerve enlargement is frequently identified, there may be marked variability in the nerve CSA both between-patients and within a patient. In some cases there may be massive enlargement (figure 3), but in other patients nerve calibre may be normal or mildly enlarged. Variability in nerve enlargement may be seen when different nerves of the same patient are compared and along the course of the same nerve, and identifying intranerve and internerve variability of CSA may be of diagnostic benefit.51
Three separate classes of US morphological findings have been described in CIDP depending on the CSA and echogenicity.52 Class 1 nerves were enlarged with hypoechoic fascicles. Class 2 nerves were enlarged with mixed hypoechoic and hyperechoic fascicles. Class 3 nerves were of normal calibre but demonstrated abnormal hyperechoic fascicles, which were less easily distinguished from the perineurial connective tissue. The nerve US patterns correlated with disease duration (class 3 was associated with longer disease duration). As such, variations in US findings in CIDP may reflect different pathophysiological stages of the disease, although further histopathological correlation is needed. As CIDP is a chronic, segmental disorder often with a relapsing course, it is expected that different classes of nerve changes may coexist in some patients.
Nerve vascularity may also be increased in patients with CIDP as assessed with Doppler US studies (figure 3).53 Nerve blood flow strongly correlates with cerebrospinal fluid protein and the number of enlarged nerves, suggesting that nerve vascularity may reflect disease activity.
The correlation between the US findings and neurophysiology features or functional disability remains controversial,43 ,52 although correlation between the extent of nerve enlargement and the duration of the disease has been reported.15 ,52 More detailed comparisons between US, clinical and neurophysiological findings are needed to clarify this point. Nerve US abnormalities may improve with treatment response.45
The extent and nature of US abnormalities in CIDP variants are less well defined, although changes overlap with typical CIDP.
Multifocal acquired demyelinating sensory and motor neuropathy
Patients with MADSAM present with asymmetric motor and sensory deficits, often with patchy neurophysiological abnormalities in nerve conduction studies. US demonstrates multifocal nerve enlargements (figure 3) that may be identified at sites of current or previous electrophysiological conduction blocks.54
Distal acquired demyelinating symmetric neuropathy
The US features of DADS have not been systematically studied. Neuropathy associated with antimyelin-associated glycoprotein (MAG) antibodies is most commonly categorised with DADS and one study has evaluated US findings in this patient population.55 Patchy enlargement of nerves was identified most commonly at entrapment sites. Of interest, distal nerve enlargement was not prominent and this contrasts with the characteristic neurophysiological findings of prominent slowing of distal nerve conduction.56
The demyelinating neuropathy associated with POEMS (polyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes) syndrome may be confused with CIDP early in the course of the disease. Distinguishing clinical features include poor treatment response and the associated systemic features that contribute to the acronym. Increased serum vascular endothelial growth factor is a marker of the disease. US may also help distinguish POEMS syndrome neuropathy from CIDP. In POEMS syndrome, nerve enlargement may be seen at sites of nerve entrapment but is uncommon in other parts of the nerve,57 which is distinct from the findings in CIDP.
Multifocal motor neuropathy
Multifocal motor neuropathy (MMN) is a rare neuropathy characterised by slowly progressive limb weakness, most commonly starting in the distal upper limb, with most patients responding to treatment with intravenous immunoglobulin. From a practical perspective, in some cases MMN can be difficult to distinguish from patients with progressive muscular atrophy. US studies identify focal nerve enlargement in the majority of patients with MMN, including in limbs without neurophysiological dysfunction.45 ,58 ,59 This is in contrast to the mild reduction of nerve CSA seen in MND.60 As such, US studies have been suggested as one method to select appropriate patients for treatment.28
Presently, there are few studies reporting the US findings in patients with Guillain-Barré syndrome (GBS) and no studies to date comparing demyelinating with axonal GBS variants. Nerve enlargement has been reported in 47–83% of patients with early GBS, and may be present in peripheral nerves and/or cervical nerve roots.15 ,61 The distribution of nerve changes may be patchy within an individual61 and may be seen early before neurophysiological changes have developed.15 Alterations of the fascicular architecture have been reported, with heterogeneous focal enlargement of single fascicles noted in one case report.62
In a detailed study, Gallardo et al61 described clinical, neurophysiological and US findings in six consecutive early GBS patients, with pathological correlation with autopsy material in two patients. US of the cervical nerve roots, and major upper and lower limb peripheral nerves was reported. US abnormalities were only detected in 8.8% of the scanned nerves, however, cervical nerve root abnormalities were identified in the majority of patients, consisting of increased CSA and reduced definition of epineurial margins. Indistinct margins of cervical nerve roots was a novel US finding and was correlated with nerve oedema demonstrated on corresponding pathological studies, which suggested that US findings may reflect the pathogenesis of the disease.
While longitudinal studies are generally lacking, a single case report demonstrated that US changes normalised during recovery, in keeping with clinical and neurophysiological improvement.62 However, increased nerve CSA was identified in patients with residual deficits years after the onset of GBS, but these US changes did not correlate with functional disability.63
Leprosy is the most common infectious cause of neuropathy worldwide. Nerve enlargement and loss of fascicular pattern are seen on US.27 ,64 These abnormalities are most frequent at common sites of nerve entrapment, in particular the cubital tunnel. However, generally the nerve enlargement tends to be more extensive and less circumscribed. Thickened and hypoechoic epineurium is a characteristic finding. Immunologically mediated reversal reactions are a common cause of skin and nerve injury in leprosy, and Doppler US at this stage may demonstrate increased nerve vascularity, which suggests rapid progression of nerve damage and a poor prognosis.64
The role of US may be less well defined in axonal PN. Intuitively, one may expect reduced CSA in axonal PN due to loss of myelinated fibres. However, this is seldom apparent with the exception of modest reduction of nerve calibre in amyotrophic lateral sclerosis (ALS).60 ,65 ,66 In fact, US of axonal PN may detect nerve enlargement in approximately 20% of patients.15
Studies of US in diabetic PN, most of them focused on the evaluation of tibial and median nerves, have demonstrated evidence of nerve and fascicle enlargement, and loss of fascicular pattern.67–70 Correlation with electrophysiological parameters has been noted in some but not in all studies. Specifically, inverse relationships between nerve CSA and compound muscle action potential amplitude and motor nerve conduction velocity have been identified.69 Increased water content due to conversion of glucose into sorbitol in the nerve was suggested as a cause of the increased nerve CSA.67 Nerve enlargement may be an interesting marker of diabetic PN severity in future studies, although it is noted that this finding has not been reported in all studies of diabetic PN.15 ,71
Oxaliplatin-induced neuropathy, which has axonal features on neurophysiological studies,72 is not associated with reduced CSA on US but rather nerve enlargement at sites of nerve entrapment—a finding suggesting increased susceptibility to mechanical nerve injury.73
When only imaging data is considered, hypertrophic neuropathy may be mistaken for a peripheral nerve tumour and vice versa, particularly when nerve enlargement is segmental or when tumours are multifocal, for example, neurofibromatosis, multiple schwannomatosis and intraneural perineurioma.74 ,75 A comprehensive review of US in peripheral nerve tumours is beyond the scope of this review (and readers are directed to specific reviews on the topic76 ,77). However, characteristic lesion features are noted in some peripheral nerve tumours, which may help distinguish them from hypertrophic neuropathy. A comprehensive US study of proximal and distal peripheral nerves combined with clinical and neurophysiological information should satisfactorily distinguish each disease process; however, fascicular nerve biopsy may sometimes be needed.
Practical approach to US diagnosis
Mapping nerve abnormalities
An important aspect of the US examination of suspected PN is analysis of the topographic distribution of nerve abnormalities. This includes: the number of nerves involved (diffuse, multifocal or localised); the presence of a proximal or distal predominance; and the uniformity of the involvement along the course of the nerve. Comprehensive US assessment of the peripheral nervous system is the recommended approach, which may include examination of the brachial plexus, upper extremity nerves (median, radial and ulnar) and lower extremity nerves (femoral, sciatic, peroneal, tibial and sural), with the composition of the study guided by the clinical phenotype but also including clinically unaffected regions.
Distinguishing CMT from CIDP
One issue experienced in the neuromuscular clinic is distinguishing some acquired neuropathies from hereditary demyelinating neuropathies and broad diagnostic test batteries and empirical treatment trials are often employed to confirm a diagnosis. Nerve US may contribute to the diagnosis of demyelinating neuropathies in a number of ways.
US may help differentiate CMT from mimicking acquired demyelinating neuropathies, such as in those patients in whom clinical features and nerve conduction studies remain inconclusive. Evaluation of CSAs at intermediate nerve segments helped distinguish demyelinating CMT from CIDP because the CSAs in patients with demyelinating CMT were uniformly enlarged while those in patients with CIDP demonstrated variable enlargement.78 However, care must be taken because patients with demyelinating CMT other than CMT1A do not always exhibit nerve enlargement.32
In addition, US studies facilitate assessment of proximal nerve segments that may be difficult to assess with nerve conduction studies, and hence may improve the detection of PN with demyelinating features in a predominantly proximal distribution.
Identifying the contribution of nerve compression
Despite non-specific findings in patients with axonal PN, US does have an important role in the diagnosis or exclusion of superimposed entrapment neuropathy in these patients, which can be difficult to diagnose using electrophysiological studies alone. US is able to confirm the diagnosis of compressive neuropathy and to rule out anatomical contributions to nerve injury.
As an example, increased CSA of the median nerve without change in wrist-to-forearm ratio might be compatible with diabetic PN, while it would not be indicative of carpal tunnel syndrome.79 Many causes of PN do not lead to altered nerve morphology on US, but may predispose to secondary entrapment neuropathy. For example, 70% of patients with systemic sclerosis and sensory complaints have US evidence of carpal tunnel syndrome or ulnar neuropathy at the elbow.80
Future directions: beyond CSA
Recent publications have demonstrated the utility of US in the work-up of patients with PN. However, many studies to date have examined heterogeneous populations. In addition, most studies have focused on the measurement of CSA at different sites, and there is overlap of values with healthy populations. Unlike findings in entrapment mononeuropathy, there is frequently no correlation between the changes in nerve calibre in PN and clinical severity, although detailed clinical information is often not reported. More detailed exploration of the US changes in PN may provide a more powerful assessment of nerve pathology, which may help in the diagnosis of PN.
The high resolution of US allows accurate assessment of different morphological characteristics of the nerve independent of CSA and these features have seldom been mentioned in published studies. The features that may warrant further exploration include: fascicle diameter, fascicle-to-connective tissue ratio, epineurial demarcation and nerve blood flow.23 ,52 ,53
Proposed classification of nerve US abnormalities
Although the angle of insonation and other technical factors impact on the nature of the nerve image acquired by US, information regarding the histopathological processes occurring within the nerve may be available with closer scrutiny of the US appearance of the nerve. Taking into account the different morphological aspects that can be evaluated at present, the previous reports and our personal observations, we propose the following patterns of nerve involvement (figure 2):
Type 1: Increased CSA in multifascicular nerves due to fascicular enlargement.
Type 1a: With uniform or heterogeneous enlargement of hypoechoic fascicles as seen in hereditary demyelinating neuropathies and CIDP.
Type 1b: With mixed hyperechoic and hypoechoic fascicles as seen in longstanding CIDP.
Type 1c: With obliteration of normal sonographic fascicular appearance as seen in inflammatory PN, nerve trauma, HNPP, leprosy and some axonal neuropathies; mild examples of this pattern are also common in entrapment sites in nerves of asymptomatic normal individuals.
Type 2: Increased CSA in monofascicular nerves. This pattern may be seen in the brachial plexus and cervical nerve roots in inflammatory neuropathies, such as GBS and CIDP, and hereditary neuropathies such as CMT.
Type 3: Increased CSA in multifascicular nerves due to increased perineurial connective tissue. This may be seen in unusual neuropathies, such as hypertrophic mononeuropathy and leprosy, and may contribute to US changes in diabetic neuropathy.
Type 4: Normal CSA with fascicular enlargement or altered echotexture as seen in CIDP and deposition disorders such as amyloid neuropathy.
Type 5: Decreased CSA. Reduced CSA has been reported in ALS and rarely in studies of patients with axonal PN.
US has a complementary role in the diagnosis of PN. US has the advantage of excellent resolution of superficial nerves, and the dynamic nature of image acquisition makes it a natural fit for the neuromuscular and electrodiagnostic clinics. Neurophysiological studies have long been considered to be an extension of the clinical examination.81 It is expected that a similar assertion will be increasingly relevant for US, and the addition of anatomic and structural information may provide important complementary diagnostic information.
Further, US may be useful to distinguish between different types of neuropathy, in particular the demyelinating neuropathies, by identifying patterns of morphological changes. Incorporating US features into diagnostic algorithms may rationalise the process of diagnostic testing with inherent time and cost savings. Exploration of nerve US features in addition to CSA may provide additional pathophysiological and diagnostic insights. Further correlation between US and MRI in PN may allow the roles of each of these techniques to be better delineated.
Presently, correlations between nerve morphology and electrophysiological function are emerging in demyelinating neuropathies, such as CMT and CIDP, and diabetic neuropathy; however, further exploration is needed to determine the relationship between structure and function in other neuropathy subtypes. Understanding of this emerging diagnostic tool will be better developed by detailed comparisons of US findings with clinical, neurophysiological and histopathological features, and this is recommended as a focus of future research.
NGS gratefully acknowledges funding from the National Health and Medical Research Council and the Motor Neurone Disease Research Institute of Australia (grant #1039520).
Competing interests None.
Provenance and peer review Commissioned; externally peer reviewed.
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