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    MR Imaging of the Lower Leg versus Clinical Electrophysiologic Examination in the Differential Diagnosis of Neurogenic Foot Drop | American Journal of Neuroradiology  
    


















    


























    
  
  




    
    

  

      


    

      

  
  
  

    

  

    

  

                
    

      

  

    

  
      
  
  

    


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EditorialEDITORIAL

  
      

  
      
MR Imaging of the Lower Leg versus Clinical Electrophysiologic Examination in the Differential Diagnosis of Neurogenic Foot Drop
  
    	
Ram Ayyar

  
    	
American Journal of Neuroradiology August 2003,  24 (7) 1273-1274; 

  
  
  



  


  
  



  
      
  
  

    
Patients with foot drop are frequently seen in clinical practice. Foot drop may be due to a lesion of the common peroneal nerve, L5 radiculopathy, or a partial sciatic nerve lesion or lesions involving the lumbosacral plexus or cauda equina. Nerve conduction studies and electromyography (EMG) are of great help in localizing the site of the lesion. EMG can help detect evidence of denervation in foot drop of recent onset and can also help in establishing evidence of reinnervation in more chronic lesions.
Since the description by Polak et al (1) of significant MR signal intensity changes in denervated muscles, several other articles have been published documenting MR signal intensity changes in the denervated muscles. An article by Bendszus et al in this issue of the AJNR compares MR findings of the lower leg with those of clinical and electrophysiologic examination in the differential diagnosis of neurogenic foot drop (2). In a prospective study with a total of 40 patients, 20 had peroneal nerve lesions, nine had L5 radiculopathy, and 11 had other lesions to account for the foot drop. MR imaging included axial T1-weighted and turbo inversion recovery magnitude (TIRM) images of the lower leg. The MR images were evaluated for patterns of signal intensity increase on TIRM images by two readers blinded to the clinical data. Three distinct patterns of signal intensity increase on TIRM images were noted: peroneal nerve pattern, L5 pattern, and nonspecific pattern. T1-weighted images were used for localizing the muscles. The electrophysiologic studies were performed within a week after MR studies. MR imaging and EMG were in agreement in 37 of the 40 patients. In three patients, MR imaging demonstrated a more widespread involvement than did EMG. In one of the patients with combined L5 and S1 radiculopathy, evidence of denervation was noted on MR images, but not on EMG, because only one of the two heads of gastrocnemius muscle was studied by EMG. In another patient who had a lesion of the peroneal nerve, MR imaging showed increased signal intensity on TIRM images in the distal parts of the anterior tibial compartment muscles, whereas the proximal anterior compartment muscles were normal. EMG showed no evidence of denervation, and repeat study showed evidence of denervation only in the distal parts of the muscles. On the basis of their findings, the authors claim that, in selected patients with acute and subacute denervation, MR imaging may be more accurate than EMG in the differential diagnosis of peripheral nerve lesions. Failure to examine sufficient numbers of muscles is a frequent cause for not detecting denervation on EMG. It is preferable to examine at least three muscles innervated by the same segment and three muscles innervated by the same peripheral nerve. It is also important to examine different parts of the same muscle.
MR imaging offers several advantages. It is noninvasive and is more easily tolerated by children. As a rule, EMG is not performed in patients receiving anticoagulants or with a bleeding diathesis. The entire cross section of the muscles can be studied by MR imaging, whereas all areas of the muscle are not examined by EMG. MR imaging can determine the degree of atrophy, hypertrophy, and fatty replacement of muscle fibers. In addition, there does not appear to be an interobserver variation in the interpretation of MR findings.
There are also some disadvantages to MR imaging. The more proximal muscles innervated by the same segments were not examined by MR imaging. Although evidence of acute and subacute denervation is easily seen, it does not apply to chronic neurogenic changes.
During EMG, several proximal and distal muscles can be examined, and paraspinal muscle evaluation may add additional information and help in the differential diagnosis of lesions of the lumbosacral plexus and cauda equina. In addition to evidence of denervation, reinnervation changes can be documented by EMG. Sensory nerve conduction studies are very helpful in differentiating lesions proximal to the dorsal root ganglion (DRG) from lesions that are distal to DRG. The sensory nerves are tested distally, and the sensory nerve action potentials will be abnormal in lesions distal to the DRG because of the interruption, anatomic or physiologic, of the distal sensory fibers from their cells of origin in the DRG. EMG is an invasive procedure, and there is a certain degree of discomfort associated with it. The expertise of the electromyographer plays a major role in the quality of the studies.
In a study comparing MR imaging of denervated muscle and EMG by McDonald et al (3), MR imaging had a relative sensitivity of 84% and specificity of 100% for detecting denervation. Increased MR signal intensity corresponded closely with evidence of denervation on EMG. They concluded that, although less sensitive than EMG in detecting muscle denervation, MR changes in signal intensity of denervated muscles were useful as adjunctive diagnostic tools in that setting.
There has been considerable excitement in the past several years about MR imaging of peripheral nervous system. The studies by Maravilla and Bowen (4) have proved to be valuable not only in localizing the anatomic site of the lesion, but also in determining the nature of the likely pathologic condition. With future advances in technology, it is likely that we will be able to arrive at a correct diagnosis in many patients with unexplained lesions of the peripheral nervous system
MR signal intensity changes in detecting muscle denervation seem to be a useful technique and can be used in addition to EMG. Whether the MR technique will be used routinely in the future remains to be seen.
References
  1. Polak JF, Jolesz FA, Adams DF. Magnetic resonance imaging of skeletal muscle: prolongation of T1 and T2 subsequent to denervation. Invest Radiol 1988;23:365–369
  2. Bendszus M, Wessig C, Reiners K, et al. MR imaging of the lower leg compared to the clinical and electrophysiologic examination in the differential diagnosis of neurogenic foot drop. AJNR Am J Neuroradiol 2003;24:1283–1289
  3. McDonald CM, Carter GT, Fritz C, et al. Magnetic resonance imaging of denervated muscle: comparison to electromyography. Muscle Nerve 2000;23:1431–1434
  4. Maravilla KR, Bowen BC. Imaging of the peripheral nervous system: evaluation of peripheral neuropathy and plexopathy. AJNR Am J Neuroradiol 1998;19:1011–1023
  


  
  



  



    

  



  

                
    

      

  

    

  
      
  
  

    


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