Abstract
Three-dimensional diffusion-weighted steady-state free precession (3D DW-SSFP) of high-resolution magnetic resonance has emerged as a promising method to visualize the peripheral nerves. In this study, the application value of 3D DW-SSFP brachial plexus imaging in the diagnosis of brachial plexus injury (BPI) was investigated. 33 patients with BPI were prospectively examined using 3D DW-SSFP MR neurography (MRN) of brachial plexus. Results of 3D DW-SSFP MRN were compared with intraoperative findings and measurements of electromyogram (EMG) or somatosensory evoked potentials (SEP) for each injured nerve root. 3D DW-SSFP MRN of brachial plexus has enabled good visualization of the small components of the brachial plexus. The postganglionic section of the brachial plexus was clearly visible in 26 patients, while the preganglionic section of the brachial plexus was clearly visible in 22 patients. Pseudomeningoceles were commonly observed in 23 patients. Others finding of MRN of brachial plexus included spinal cord offset (in 16 patients) and spinal cord deformation (in 6 patients). As for the 3D DW-SSFP MRN diagnosis of preganglionic BPI, the sensitivity, the specificity and the accuracy were respectively 96.8%, 90.29%, and 94.18%. 3D DW-SSFP MRN of brachial plexus improve visualization of brachial plexus and benefit to determine the extent of injury.
Similar content being viewed by others
Introduction
Brachial plexus injury (BPI) is the most severe nerve injury of the upper extremities and is often associated with trauma such as, motorcycle accidents1. The factors on the restricted recovery of upper limb function, especially those of the hand, after BPI are complicated. Recovery is mainly determined by the interval between injury and treatment times2, which in turn depends on early diagnosis. Early reconstructive surgery of brachial plexus injuries encourages rapid regeneration and repair3,4. However, the early determination of the degree of damage, the time of surgery, and the selection of surgical methods in BPI patients still pose problems. Patients with brachial plexus injuries are typically observed for three to six months to confirm that there is no recovery of function before surgical treatment5. However, brachial plexus root avulsions usually require surgical intervention as soon as possible6,7. A deferred diagnosis misses the best timing for early intervention. Traditionally, brachial plexus injury has been evaluated using clinical history, physical examination, and neurophysiological testing8. Neurophysiological tests and physical examination may not reveal the extent of the injury at the early stage and therefore may not supply the guideline of surgery time.
Imaging of the brachial plexus has progressed from plain radiography to CT, and then to CT myelography. Now, CT myelography has gradually been replaced by MR neurography (MRN), which is a non-invasive technique that allows assessment of both the proximal and distal components of the brachial plexus9. Since MRN was introduced in 199210, it has gained acceptance as an important diagnostic adjunct to the clinical evaluation of BPI11,12. The major disadvantage of conventional MRI sequences used to evaluate the brachial plexus was that maximum intensity projection (MIP) can be done but with less image quality13. With recent improvements in MRI, especially 3.0-T MRI, images now show 3D high-resolution views of fine structures which plays a vital role in successful preoperative diagnosis of BPI. This in turn is imperative for proper decisions to be made by surgeons14. Current state-of-the-art conventional Magnetic Resonance Nerve imaging, involving 2D or 3D high-resolution T1-weighted, (fat-suppressed) T2-weighted, or short TI inversion recovery (STIR) imaging, provides detailed anatomic nerve depiction15,16. Clinical application of three-dimensional reversed fast imaging by steady-state precession (3D-PSIF) with diffusion-weighted MR sequence showed the successful use in cranial nerve reconstruction in 200817, while a review of the current imaging literature showed rare correlation between MRN results with per-operative findings in BPI. The purpose of this study is to investigate the usefulness of three-dimensional diffusion-weighted steady-state free precession (3D DW SSFP) for BPI diagnosis.
Materials and Methods
Patients
Between January 2007 and December 2012, 33 patients with brachial plexus injury (BPI) underwent pre-operative electromyography (EMG) and magnetic resonance imaging (MRI) of the brachial plexus. The actual conditions of the injury were confirmed intra-operatively. The patients included 30 males and 3 females; 21 cases with BPI on the left and 12 on the right; ages between 16 and 52 years old, given a mean age of 33.47 ± 7.41 years old; mean interval between injury and MRI examination of 3.67 ± 1.42 months; reasons for injury: 19 cases of motorcycle accidents, 10 cases of car accidents, 2 cases of falling and 2 cases of mechanical traction injuries. The ethics committee of the First Affiliated Hospital of Sun Yat-sen University approved the study. All methods were carried out in “accordance” with the approved guidelines. All patients gave written informed consent.
MRI Examination
MRI was performed using a clinical 3.0T MR imager (Magnetom Trio with TIM system, Siemens Medical Systems, Erlangen, Germany) with a standard neck and CP spine array coil. After conventional T1- and T2-weighted spin-echo (SE) imaging was completed, the 3D-PSIF with diffusion-weighted sequence was performed. The patient was supine and the cervical spine was in the conventional position. The magnetic field was centered on the C6 vertebra and conventional neck MRI scans were performed. Patients were advised to avoid swallowing as much as possible during the scan and to breathe mainly from the abdomen. If patients had upper limb spasms due to causalgia, appropriate analgesics and sedatives were administered before the examination in order to prevent image interference caused by involuntary limb movements.
The basic parameters of the 3D DW SSFP sequence were as follows: TR 9.26 ms, TE 4.91 ms, matrix: 448 × 448 mm, flip angle, 180°, FOV, 280 × 280 mm; bandwidth, 686 Hz/px; slice thickness, 2 mm, in-plane spatial resolution, 1.1 × 1.5 mm; number of acquisitions, 2; and the acquisition time was 5 minutes 42 seconds.
The 3D DW SSFP sequence was assessed by two experienced radiologists at the same time. MR images were reviewed in a random fashion and all imaging parameters were unknown to the observers.
Observation and Evaluation
MRI observation and evaluation of normal brachial plexus: the contralateral side was used as a normal reference. The imaging features of the contralateral brachial plexus were observed in all patients with the assistance of a qualified radiologist. All clearly visible intraspinal brachial plexus roots, ganglia, and extraspinal brachial plexus roots, trunks, branches and cords were counted. MRI observation and evaluation of BPI: The MRI features of patient’s BPI were observed and analyzed, followed by comparisons with intraoperative findings and EMG or SEP.
Results
Results of MRI observation and evaluation of normal brachial plexus
MRI observations of normal brachial plexus
The brachial plexus exhibited high signal intensity in the raw MRI images while the ganglions appeared as hyperintensities. Of the 33 patients in this study, the postganglionic section of the brachial plexus was clearly visible in 26 patients, while the preganglionic section of the brachial plexus was clearly visible in 22 patients. The imaging features were as follows:
MRI features of preganglionic brachial plexus
The ventral rootlets appeared as low-signal narrow, striped shadows, which swelled to form ganglia near the intervertebral foramen, appearing as hyperintensities. The ventral rootlets could be observed clearly in the coronal view of MRI (Fig. 1), while the ganglia could be observed clearly in sagittal view (Fig. 2).
MRI features of postganglionic brachial plexus
Postganglionic brachial plexus appeared as a cord-like hyperintensities structure starting next to the intervertebral foramen between C5–8 and T1, merging under the clavicle and the axilla. The C5–8 and T1 nerve roots as well as the superior, middle and inferior trunks formed by their merging were clearly visible. The nerve branches and cords could also be seen, however, due to the higher concentration of anatomical structures, single branches or single cords could not be differentiated.
MRI count results of normal brachial plexus
The MRI count results of the 33 patients are shown in Table 1. Visibility of the brachial plexus roots and trunks were the highest, followed by that of ganglia, branches and cords, while that of the intraspinal nerve filaments were the lowest.
Results of MRI observation and evaluation of BPI
MRI Manifestation of Preganglionic BPI
Of the 33 patients, 23 had preganglionic injuries and 10 had postganglionic injuries. The results are as follows.
-
1
Pseudomeningocele: 51 cysts in 23 patients, the most common feature observed, which appeared as high-density cystic shadows inside and outside intervertebral foramen; 31 left-sided and 20 right-sided. Varied morphology, with the basic shape being triangular.
-
2
Spinal cord offset: 16 cases; 11 patients shifted toward the injured side and 5 patients shifted toward the contralateral side.
-
3
Spinal cord deformation: 6 patients. Compression from Pseudomeningocele or traction from avulsed nerve roots led to the loss of a normal oval shape of the spinal in transverse plain.
Comparison between MRI and Findings of intra-operative exploration
Among the 33 patients, 103 nerve roots were identified during surgical exploration. 96 roots were positively identified by MRI examination, of which 93 roots were true positives and 3 were false positives. Seven roots were not identified by MRI, of which 3 were false negatives and 4 were true negatives. As for the MRI diagnosis of preganglionic BPI, the sensitivity was 96.8%, specificity was 90.29% and accuracy was 94.18%. Chi-squared tests were used to compare the difference between MRI and findings of intra-operative exploration, P = 0.23 > 0.05, hence the difference was not significant (Table 2).
MRI Manifestation of Postganglionic BPI
Of the 33 patients, postganglionic brachial plexus was clearly visible in 26. The results of observation are as follows:
-
1
Nerve discontinuity, retraction of distal nerves after rupture, disappearance of local nerve structure, replacement by scar tissue or hematoma, and neural appearance could not be observed on MRI (Fig. 3).
-
2
Abnormal neural signals often manifested as hyperintensities T2-weighted images, significant neural thickening, and unclear boundaries between thickened nerves (Fig. 4a).
-
3
Abnormal shapes in neural pathways, loss of normal smooth neural pathways, meandering or even curling pathways (Fig. 5).
-
4
Abnormal signals from soft tissues surrounding the damaged nerve, including (1) scarring of the anterior scalene muscle, (2) local scarring around damage nerves, appeared as hyperintensities in T2 images.
Discussion
Anatomy of the brachial plexus
The brachial plexus innervates the muscles, joints and skin of the shoulder and upper limb. It is formed by the ventral rami of C5–C8 and T1 nerves. There is irregular contribution from the C4 and T2 rami in a pre or post fixed plexus, respectively. The C5 and C6 roots join to form the superior trunk, the C7 root forms the middle trunk and C8 and T1 roots join to form the inferior trunk. Each trunk gives anterior and posterior divisions. The posterior divisions of all the three trunks join to form the posterior cord. The anterior divisions of superior and middle trunks form the lateral cord. The anterior division of the inferior trunk forms the medial cord. The axillary and radial nerves are the terminal branches of the posterior cord. The musculocutaneous nerve and lateral root of the median nerve arise from the lateral cord. The medial root of median nerve, ulnar nerve and medial cutaneous nerves in the arm and forearm arise from the medial cord18.
3D-imaging technology of MRN
The MRN protocol includes a combination of T1W, T2W, STIR, 3D STIR SPACE and 3D T2 SPACE sequences. Recently, the integration of peripheral nerve imaging sequences and post-processing 3D-reconstruction technology has become the focus of research. In 2007, Wolfgang et al.19 reported the successful reconstruction of healthy human sciatic nerve using multi-planar 3D reconstruction. Viallon et al.20 used an isotropic 3D T2 Short Term Inversion Recovery (STIR) sequence to image normal brachial plexus and brachial plexus tumors and visualize the relationship between the brachial plexus tumors and nerves. P. Mürtza21 reported that Diffusion-weighted MRN is superior for lumbosacral plexus, but not for brachial plexus. Zhang et al.22 designed a sequence based on 3D DW-SSFP which was able to visualize the main trunk and branches of the cranial nerve. Compared to other gradient echo sequences, the echo signals of 3D DW-SSFP are produced by radio frequency (RF) excitation, which has obvious T2 contrast characteristics. As the echo signals are produced by RF excitation, the spin relaxation is less affected by inhomogeneity in the magnetic field. Thus, the advantages of 3D DW-SSFP in neuroimaging are as follows: firstly, the echo signals obtained by the gradient echo using this sequence has T2 contrast characteristics which can achieve sufficiently high resolution within a reasonable scan time while relatively less affected by inhomogeneity within the magnetic field. Furthermore, by applying water excitation for fat suppression, it is less affected by chemical shift, while the application of the diffusion gradient method allows for effective fluid suppression23. Secondly, the sequence involves 3D Fourier imaging, which allows us to obtain any level of image after various post-processing of the raw image. In addition, as the SSFP signal requires certain steady-state conditions, the proton spin of motion, such as that of blood flow, will be manifested as signal loss24, which is extremely important in the imaging of small nerves, especially when they are located among larger surrounding blood vessels.
We attempted to use this sequence in the imaging of the brachial plexus and obtained clear images showing the various sections of the brachial plexus with stable imaging in this study.
MRI features of BPI and their clinical significance
Pre-ganglionic injuries
In pre-ganglionic injuries, approximately 20% of the patients show altered signal intensity in the spinal cord on the affected side due to edema, hemorrhage or myelomalacia25. In this study pseudomeningocele is the most common finding in MRI. It is an indirect sign of preganglionic injury, well appreciated on T2 WI. The formation mechanism is the outflow of cerebrospinal fluid due to avulsion of the nerve sheath tumor, indicating the presence of nerve root avulsion26. Pseudomeningoceles may occur alone without root avulsion in 15% of the cases, and conversely, 20% of nerve root avulsions will not have a pseudomeningocele27. In this study, 5 cases with nerve root avulsions did not have a pseudomeningocele and 8 cases without pseudomeningocele proved to be root avulsion by intra-operative neurophysiological testing. Other signs of root avulsion in this study include enhancement of intradural nerve roots or root stumps. This feature was not only found on plane of the nerve root injury, it was also found in adjacent uninjured planes, which might have been due to the outward traction of the brachial plexus during injury.
Direct visualization of the intradural nerve roots is not always adequate, with reported accurate diagnosis in 52% of cases28. Obvious loss of ganglia compared to the contralateral side is mostly observed on the coronal view. Normal ganglia are manifested as round areas with high signal intensities in MRI. Their diameters are slightly larger than those of nerve roots and multiple ganglia are arranged longitudinally. After BPI the features disappeared on the affected side, while there was hyperintensities over a larger area at the ganglia compared to that on the unaffected side. Another indirect sign of preganglionic injury was spinal cord signal intensity changes29 which is observed in approximately 20% of patients with preganglionic injuries. We found spinal cord offset and deformation in 8 cases. The spinal cord could be toward the injured or contralateral side. The mechanism is due to the rupture of nerve roots or cord ligament after violent avulsion of the spine. Complete rupture will cause a shift towards the contralateral side, while a partial rupture will cause a shift to the injured side (Fig. 6). The mechanism of spinal cord deformation might be due to the compression of local meningeal cysts.
Post-ganglionic injuries
The post-ganglionic plexus can be evaluated by MRI with findings suggesting neuropraxia, axonotmesis or neurotmesis30. Nerve discontinuity on MRI implied retraction of distal nerves after rupture, disappearance of local nerve structure, and replacement by scar tissue or hematoma. If these features are discovered at the early stage, immediate surgical examination will be needed and the majority of injury nerves can be directly sutured. However, if discovered slightly later, there will be heavy local scarring that is difficult to remove surgically. The distance of nerve retraction is also longer and difficult to be sutured directly, therefore it should be repaired by nerve transfer. Neural thickening and nerve continuity was still present but often manifested as hyperintensities in T2-weighted images (Fig. 7). Nerves on the injured side were obviously thicker than those on the contralateral side, while the relationship between thickened nerves was unclear. Whether surgical intervention or more conservative therapies is appropriate depended on EMG or SEP. If the EMG and SEP are positive, neurolysis would be performed, otherwise the nerve transfer would be the method used. Of the 33 patients in this study, 6 cases exhibited such manifestations. During surgical examination it was found that the nerves had slightly harder texture and electrical stimulation of the lesion caused muscle contraction, therefore only neurolysis was performed. High hyperintense signal changes of flat and long segments in T2W images implied that the differentiation between nerves and surrounding soft tissues were unclear. Such manifestations indicated more severe conditions than root avulsions and treatment was more difficult. Intraoperative examination revealed a long segment of scar tissue surrounding the nerves where the nerve defect was no more than 20 cm, and then left rare reconstructive options, such as contralateral C7 (CC7) and vascularized ulnar nerve transfer (Fig. 4b).
Effects of brachial plexus MRI on surgical selection in BPI
If MRI examinations are carried out at the early stages of BPI, which can elucidate the status of nerve damage, surgical interventions can be done at the early stage. Not only can brachial plexus MRI be used to identify preganglionic and postganglionic damage, it can also be used to localize postganglionic damage, thus providing a reference for surgical incisions. Therefore, it is imperative that patients with suspected BPI should first undergo MRI examination as soon as possible. Patients who had BPI clinical manifestation with MRI showing the continuous nerve survival and without abnormal signals of the brachial plexus when compared to the unaffected side can receive conservative treatment for three months.
Patients with the following conditions should immediately receive surgery: 1. Medical history of penetration wound with clinical manifestation of BPI, and nerve discontinuity revealed in MRI; 2. MRI reveals widespread abnormal brachial plexus signals, with unclear boundaries between nerves and surrounding soft tissues; 3. MRI indicates brachial plexus root avulsion.
Limitations
There are certain limitations to the study. One of the limitations is the small sample size. Second, it takes 30 minutes to 40 minutes to complete the examination which might increase the chance of motion artifact, especially for patients with claustrophobia. Third, division and cord segments of the brachial plexus gather into a bundle therefore, it is difficult to distinguish each nerve. Forth, due to the factors such as the cerebrospinal fluid and breathing, there is a certain rate of false positives (13%). Finally, cost might be a major problem limiting the common use of brachial plexus MRI examination.
Conclusion
Three-dimensional diffusion-weighted steady-state free precession (3D DW-SSFP MRN) improve visualization of brachial plexus from root to branch and help to determine the level of the injury and character of injury. 3D DW-SSFP MRN was demonstrated to be useful in preoperative diagnoses of the type, presurgical planning and timing of surgery for brachial plexus injuries.
Additional Information
How to cite this article: Qin, B.-G. et al. Diagnostic Value and Surgical Implications of the 3D DW-SSFP MRI On the Management of Patients with Brachial Plexus Injuries. Sci. Rep. 6, 35999; doi: 10.1038/srep35999 (2016).
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
Yang, Y. et al. Functioning free gracilis transfer to reconstruct elbow flexion and quality of life in global brachial plexus injured patients. Sci Rep 6, 22479 (2016).
Lanaras, T. I., Schaller, H. E. & Sinis, N. Brachial plexus lesions: 10 years of experience in a center for microsurgery in Germany. Microsurg 29(2), 87 (2009).
Ma, J., Novikov, L. N., Kellerth, J. O. & Wiberg, M. Early nerve repair after injury to the postganglionic plexus: an experimental study of sensory and motor neuronal survival in adult rats. Scand J Plast Reconstr Surg Hand Surg 37(1), 1 (2003).
Jivan, S., Kumar, N., Wiberg, M. & Kay, S. The influence of pre-surgical delay on functional outcome after reconstruction of brachial plexus injuries. J Plast Reconstr Aesthet Surg 62(4), 472 (2009).
Zhu, J. Recent progress in diagnosis and treatment of the injury to the peripheral nerve. Zhong guo Xiu Fu Chong Jian Wai Ke Za Zhi 20(4), 319 (2006).
Shin, A. Y., Spinner, R. J., Steinmann, S. P. & Bishop, A. T., Adult traumatic brachial plexus injuries. J Am Acad Orthop Surg 13(6), 382 (2005).
Spinner, R. J., Shin, A. Y. & Bishop, A. T. Update on brachial plexus surgery in adults. Current Opinion in Orthopaedics 15(4), 203 (2004).
Pullman, S. L. et al. Clinical utility of surface EMG: report of the therapeutics and technology assessment subcommittee of the American Academy of Neurology. Neurology 55(2), 171 (2000).
Mallouhi, A. et al. 3T MR tomography of the brachial plexus: structural and microstructural evaluation. Eur J Radiol 81(9), 2231 (2012).
Howe, F. A., Filler, A. G., Bell, B. A. & Griffiths, J. R. Magnetic resonance neurography. Magn Reson Med 28(2), 328 (1992).
Du, R. et al. Magnetic resonance neurography for the evaluation of peripheral nerve, brachial plexus, and nerve root disorders. J Neurosurg 112(2), 362 (2010).
van Es, H. W., Bollen, T. L. & van Heesewijk, H. P. MRI of the brachial plexus: a pictorial review. Eur J Radiol 74(2), 391 (2010).
Takahara, T. et al. Diffusion-weighted MR neurography of the brachial plexus: feasibility study. Radiology 249(2), 653 (2008).
Upadhyaya, V., Upadhyaya, D. N., Kumar, A. & Gujral, R. B. MR neurography in traumatic brachial plexopathy. Eur J Radiol 84(5), 927 (2015).
Thawait, S. K. et al. Peripheral nerve surgery: the role of high-resolution MR neurography. AJNR Am J Neuroradiol 33(2), 203 (2012).
Eppenberger, P., Andreisek, G. & Chhabra, A. Magnetic resonance neurography: diffusion tensor imaging and future directions. Neuroimaging Clin N Am 24(1), 245 (2014).
Zhang, Z. et al. 3-T imaging of the cranial nerves using three-dimensional reversed FISP with diffusion-weighted MR sequence. J Magn Reson Imaging 27(3), 454 (2008).
MusetiLara, A., Dolz, C. & Rodriguez-Baeza, A. Anatomy of the brachial plexus. (ed. Gilbert, A. ) 3–15 (Martin, 2001).
Freund, W. et al. MR neurography with multiplanar reconstruction of 3D MRI datasets: an anatomical study and clinical applications. Neuroradiology 49(4), 335 (2007).
Viallon, M. et al. High-resolution and functional magnetic resonance imaging of the brachial plexus using an isotropic 3D T2 STIR (Short Term Inversion Recovery) SPACE sequence and diffusion tensor imaging. Eur Radiol 18(5), 1018 (2008).
Murtz, P. et al. Diffusion-weighted MR neurography of the brachial and lumbosacral plexus: 3.0 T versus 1.5 T imaging. Eur J Radiol 84(4), 696 (2015).
Zhang, Z., Chen, Y. & Meng, Q. Imaging of cranial nerves with three-dimensional high resolution diffusion-weighted MR sequence based on SSFP technique. International Journal of Medical Radiology 31(1), 1 (2008).
Baur, A. et al. Diffusion-weighted MR imaging of bone marrow: differentiation of benign versus pathologic compression fractures. Radiology 207(2), 349 (1998).
Taupitz, M. et al. T2-weighted breath-hold MR imaging of the liver at 1.5 T: results with a three-dimensional steady-state free precession sequence in 87 patients. Radiology 194(2), 439 (1995).
Abul-Kasim, K., Backman, C., Bjorkman, A. & Dahlin, L. B. Advanced radiological work-up as an adjunct to decision in early reconstructive surgery in brachial plexus injuries. J Brachial Plex Peripher Nerve Inj 5, 14 (2010).
Castillo, M. Imaging the anatomy of the brachial plexus: review and self-assessment module. AJR Am J Roentgenol 185 (6 Suppl), S196 (2005).
van Es, H. W., Bollen, T. L. & van Heesewijk, H. P. MRI of the brachial plexus: a pictorial review. Eur J Radiol 74(2), 391 (2010).
Romano, A. et al. Intravenous injection of bortezomib, melphalan and dexamethasone in refractory and relapsed multiple myeloma. Ann Oncol 24(4), 1038 (2013).
Sureka, J., Cherian, R. A., Alexander, M. & Thomas, B. P. MRI of brachial plexopathies. Clin Radiol 64(2), 208 (2009).
Caranci, F. et al. Magnetic resonance imaging in brachial plexus injury. Musculoskelet Surg 97 Suppl 2, S181 (2013).
Acknowledgements
The authors acknowledge the NHFPC Special Fund for Health Scientific Research in the Public Welfare (Number 201402016). We thank Audra Heinitz (Tomas hospital, TN, USA) for the English improvement.
Author information
Authors and Affiliations
Contributions
B.-G.Q. was responsible for conception and design, acquisition of data and drafting the article; B.Q. and J.-T.Y. contributed equally to this study. J.-T.Y. contributed to analysis and interpretation of data; Y.Y. contributed to analysis, interpretation of data and English language polishing; H.-G.W. revised the article; G.F. was responsible for English language polishing. L.-Q.G. was responsible for conception and design, acquisition of data; P.L. contributed to analysis and interpretation of data; Q.-T.Z. revised the article; X.-L.L. acquired data; J.-K.Z. revised the article.
Ethics declarations
Competing interests
The authors declare no competing financial interests.
Rights and permissions
This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
About this article
Cite this article
Qin, BG., Yang, JT., Yang, Y. et al. Diagnostic Value and Surgical Implications of the 3D DW-SSFP MRI On the Management of Patients with Brachial Plexus Injuries. Sci Rep 6, 35999 (2016). https://doi.org/10.1038/srep35999
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/srep35999
This article is cited by
-
Development of magnetic resonance imaging of brachial plexus neuralgia
Neurological Sciences (2022)
-
MR neurography in traumatic, non-obstetric paediatric brachial plexopathy
European Radiology (2018)
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.