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Neurogenic muscle hypertrophy following L5 motor radiculopathy
  1. Mary Clare McKenna1,
  2. Eavan McGovern2,
  3. Michael Farrell3,
  4. Ronan P Killeen4,
  5. Chris McGuigan2,
  6. Sean Connolly1
  1. 1 Clinical Neurophysiology Department, St Vincent's University Hospital, Dublin, Ireland
  2. 2 Neurology Department, St Vincent's University Hospital, Dublin, Ireland
  3. 3 Neuropathology Department, Beaumont Hospital, Dublin, Ireland
  4. 4 Radiology Department, St Vincent's University Hospital, Dublin, Ireland
  1. Correspondence to Dr Mary Clare McKenna, Clinical Neurophysiology Department, St Vincent's University Hospital, Dublin 4, Ireland; mary.mc-kenna.1{at}ucdconnect.ie

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Case

A 59-year-old man developed progressive swelling, stiffness and pain in the right anterior leg, 3 years after a right L4–L5 discectomy that had fully resolved his radicular symptoms. An anterior tibial fasciotomy, for presumed compartment syndrome, failed to lessen his symptoms. On examination, there was marked hypertrophy of the right anterior tibial musculature resulting in a 3 cm difference in leg circumference (figure 1). This limited his range of ankle joint movement, but there was no weakness. His serum creatine kinase was elevated (400 IU/L, normal <70), MR scan of the lower legs showed markedly enlarged right tibialis anterior muscle and biopsy of this muscle showed fibre splitting, fibre hypertrophy and central nuclei (figure 2). With no fibre-type grouping, the biopsy could not confirm reinnervation. His first electromyography (EMG) appointment was 3 years after the onset of the swelling, which had continued to worsen. Continuous complex repetitive discharges were recorded from all sites in the resting right tibialis anterior that were studied by concentric needle EMG (figure 3). The discharges occurred spontaneously and were also enhanced by needle movement. Jitter between individual action potentials within the complex repetitive discharges complexes, measured using single fibre EMG, was often very low (figure …

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Footnotes

  • Contributors MCM was involved in study design, data analysis and drafting the manuscript. EM, MF, CM and RK were involved in the clinical care of the patient, data analysis, critical review and final approval of the manuscript. SC was involved in the clinical care of the patient, data acquisition, data analysis, supervising, critical review and final approval of the manuscript.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed by Jon Walters, Swansea, UK.

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