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Neuromuscular Ultrasound: A New Tool in Your Toolbox

Published online by Cambridge University Press:  20 September 2018

Nens van Alfen*
Affiliation:
Department of Neurology and Clinical Neurophysiology, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands
Jean K. Mah
Affiliation:
Departments of Pediatrics and Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Alberta Children’s Hospital, Calgary, Alberta, Canada
*
Correspondence to: N. van Alfen, Department of Neurology 920, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, PO Box 9101, 6500 HB Nijmegen, The Netherlands. Email: nens.vanalfen@radboudumc.nl
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Abstract

Neuromuscular ultrasound is a rapidly evolving technique for diagnosing, monitoring and facilitating treatment of patients with muscle and nerve disorders. It is a portable point-of-care technology that is non-invasive, painless and without ionizing radiation. Ultrasound can visualize muscle texture alterations indicating dystrophy or denervation, changes in size and anatomic continuity of nerve fascicles, and its dynamic imaging capabilities allow capturing of contractions and fasciculations. Ultrasound can also provide real-time guidance for needle placement, and can sometimes make a diagnosis when electromyography is not tolerated or not informative anymore. This review will focus on the technical and practical aspects of ultrasound as an imaging technique for muscles and nerves. It will discuss basic imaging principles, hardware and software setup, and provide examples of ultrasound use for visualizing muscle and nerve abnormalities with accuracy and confidence. The review is intended as a practical “how-to” guide to get started with neuromuscular ultrasound in daily practice.

Résumé

Les examens d’échographie dans le cas de pathologies neuromusculaires : un nouvel outil à votre disposition. Les examens d’échographie destinés aux pathologies neuromusculaires sont en mutation rapide. Ils permettent de diagnostiquer des troubles des muscles et des nerfs, d’assurer le suivi des patients atteints et de faciliter leur traitement. À la fois non-invasive et sans douleur, pouvant être utilisée sur les lieux des soins, cette technologie n’entraîne aucune radiation ionisante. De tels examens permettent ainsi de constater des altérations à la texture des muscles pouvant constituer des indices de dystrophie ou de dénervation mais aussi des modifications concernant la taille et la continuité anatomique des faisceaux nerveux. Ces capacités dynamiques d’imagerie permettent aussi de détecter des signes de contraction et de fasciculation. Ce n’est pas tout : les examens d’échographie peuvent aussi permettre un guidage en temps réel pour le positionnement d’une seringue et parfois faciliter l’établissement d’un diagnostic lorsqu’un examen d’électromyographie n’est pas toléré ou n’est plus en mesure de fournir des données utiles. Cette étude entend donc se pencher sur les aspects techniques et pratiques de ce type d’échographie destinée aux muscles et aux nerfs. Elle abordera les principes de base de l’imagerie, le type d’installation informatique requise ainsi que les logiciels utilisés. Elle fournira des exemples d’examens d’échographie permettant de détecter, avec exactitude et en toute confiance, des anomalies des muscles et des nerfs. En somme, cette étude a été conçue comme un guide pratique permettant, dans le cas de pathologies neuromusculaires, d’utiliser pour la première fois et quotidiennement des examens d’échographie.

Information

Type
Review Article
Copyright
Copyright © 2018 The Canadian Journal of Neurological Sciences Inc. 
Figure 0

Figure 1 (A) Shows a transverse image of a healthy medial gastrocnemius muscle, showing the “starry night” appearance of dark muscle fiber tissue interspersed with white speckles of fascia. (B) Shows a longitudinal image of a healthy biceps brachii muscle, showing the linear arrangement of muscle fibers that insert at an angle onto the underlying fascia and bone.

Figure 1

Figure 2 (A) Shows a transverse image of the median nerve in the forearm. The hyperechoic rim of the epineurium and the internal fascicle bundles are clearly visible. (B) Shows a longitudinal image of the median nerve in the forearm. The markers delineate the outer epineurial edge of the nerve; internally, the longitudinal lines of perineurial fascia are seen. The nerve as a whole resembles a set of railway tracks.

Figure 2

Figure 3 Two transverses images of the proximal ventroradial forearm, showing the bony structure of the radius with different muscles layered on top, and the median nerve between the fascia (arrow). Notice the difference in overall image appearance; the left image was captured with a Sonosite Xporte system with a 5-16 MHz linear probe and a MSK nerve preset (Fujifilm Sonosite Inc., Bothell, Washington, DC), and the right image was captured with an Esaote MyLab Alpha system with a 3-13 MHz linear probe and an MSK preset (Esaote SpA, Genoa, Italy).

Figure 3

Figure 4 Transverse image of the ventral wrist crease, showing the flexor tendons of the wrist and fingers and the median nerve in the middle on top. The top half of the image shows a raw image format without additional image enhancing; the bottom half shows full use of image-enhancing features with clear delineation of the nerve and tendon contours. Images captured on a Philips IU22 system with a linear 5-17 MHz probe and MSK preset (Philips Healthcare, Eindhoven, The Netherlands).

Figure 4

Figure 5 Two images of the proximal ventral forearm showing the flexor muscle overlying the radius (on the left) and ulna (right), with the median nerve in the middle left. The left image shows the result of an optimal 90° scan angle, with clear reflection of the bony edges, the fascia and outline of the nerve. The right image shows a 5° probe tilt with a resulting 85° scan angle toward the bones and fascia; the amount of ultrasound that is deflected and does not return to the probe results in a visibly darker image with suboptimal delineation of anatomical structures.

Figure 5

Figure 6 Transverse image of a normal median nerve at the level of the wrist crease, with markers indicating the internal epineurial rim and measuring the cross-sectional area. The nerve lies on top of the finger flexor tendons. The arch of the carpal ligament can be seen lying from left to right over the nerve.

Figure 6

Figure 7 Two images of the ventral forearm. The left image is unannotated, making it harder to instantly recognize the site and anatomical features. On the right is the annotated image indicating the bone, muscles and median nerve for clarity, and also showing power Doppler signals of the radial artery (RAD ART) and small arteries accompanying the median nerve. FDP=flexor digitorum profundus; FDS=flexor digitorum superficialis; PT=pronator teres.

Figure 7

Figure 8 Panel showing four examples of the visual appearance of nerve pathology. (A) Swollen ulnar nerve in the upper arm with enlarged, hypoechoic fascicles and a slightly thicker epineurium, caused by thermal injury of the nerve during surgery for a humeral fracture (osteosynthesis material is visible in the underlying bony structure). (B) Enlarged median nerve at the wrist with a very thick epineurium and an overlying subcutaneous scar, caused by repeated carpal tunnel decompressions in the context of ongoing labor-induced compression of the nerve. (C) Neuroma in continuity of the ulnar nerve in the forearm after a glass-cut injury that partially transected the nerve and encased it in scar tissue (a Sunderland mixed-grade 4/5 lesion). (D) Supraclavicular brachial plexus lying on top of the 1st rib and adjacent to the subclavian artery in a patient with active chronic inflammatory demyelinating polyneuropathy. The different plexus elements are swollen and show a typical diffusely hyperechogenic appearance. FCR=flexor carpi radialis; SA=subclavian artery.

Figure 8

Figure 9 (A) Shows a transverse image of the ventral upper leg (VL), with the rectus femoris (RF) muscle lying in the middle on top, showing the typical oblique shape of its internal central fascia. (B) Shows a transverse image of the tibialis anterior (TA) muscle scanned at a 90° angle to obtain the brightest and best reproducible depiction of the underlying interosseus membrane and equal echogenicity of both muscle halves. EDL=extensor digitorum longus; VI=vastus intermedius; VM=vastus medialis.

Figure 9

Figure 10 This panel shows three types of abnormality that can be found on visual evaluation of muscle ultrasound. On the left a diffusely increased echogenicity with a “ground glass” aspect of the biceps brachii muscle is seen. This pattern occurs in muscular dystrophies such as Duchenne muscular dystrophy (DMD) and facioscapulohumeral dystrophy (FSHD). In the middle a biceps muscle is seen with an area of increased echogenicity and other parts of the muscle that have a normal appearance. Such patchy abnormalities are mainly found in inflammatory disorders of muscle, such as dermatomyositis, but can also occasionally occur in FSHD or in disorders with very focal denervation such as neuralgic amyotrophy. On the right a biceps muscle with focal zones of normal echogenicity (the black holes) surrounded by hyperechogeneous tissue (denervated fibrosed muscle) is seen, giving it a “moth-eaten” appearance. This pattern is found in disorders with denervation and partial reinnervation of muscles, such as in spinal muscular atrophy (SMA), severe radiculopathies or inclusion body myositis.

Figure 10

Figure 11 Transverse image of a severely affected tibialis anterior (TA) muscle in facioscapulohumeral dystrophy. The intramuscular central tendon, as well as the intermuscular facia between the TA and extensor digitorum longus (EDL), now appear dark instead of bright (compare to Figure 9B). The interosseus membranes and deeper structures are no longer visible because of attenuation of the ultrasound caused by absorption and scattering of the beam.

Figure 11

Figure 12 Transverse image of the proximal dorsomedial forearm showing the radius with an overlying supinator and brachialis muscle. The echogenicity of the supinator is clearly abnormal and compatible with selective denervation caused by a partial infraclavicular brachial plexus traction injury. BR=brachioradialis; SUP=supinator.

Figure 12

Figure 13 The Heckmatt grading scale for visual assessment of muscle echogenicity. Grade 1 is normal. Grade 2 shows an overall increase in echogenicity without architecture loss or attenuation. Grade 3 showed clearly increased muscle echogenicity, loss of muscle architecture and some attenuation causing less visibility of deeper structures. Grade 4 denotes a completely white muscle with loss of recognizable features and strong attenuation of the ultrasound signal, so no deep structures can be discerned beyond the superficial layer of muscle.

Figure 13

Figure 14 This panel shows the vastus lateralis muscle in two healthy female subjects, one with a body mass index (BMI) of 18.7 (left image) and one with a BMI of 30.1 (right image). The muscle on the right has more intramuscular fat depositions, leading to a more grainy and somewhat fuzzy appearance of the intramuscular fascia.

Figure 14

Figure 15 Screenshot of the ImageJ free software program for calculating mean grayscale value from the muscle ultrasound image histogram. The rectangle in the left half of the image denotes the region of interest from which the histogram is captured.

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