• Ioannis M Skaribas and Stephanie N Washburn.
• Greater Houston Pain Consultants, Houston, TX, USA; and St. Jude Medical Neuromodulation Division, Plano, TX, USA.
• Neuromodulation. 2010 Jul 1;13(3):224-8.

Objectives  Charcot-Marie-Tooth (CMT) disease is one of the most common hereditary neuropathies affecting one in 2500 people in the United States. CMT disease is associated with moderate to severe chronic extremity pain. We present the case of a young man with chronic intractable lower extremity pain associated with CMT disease treated with spinal cord stimulation (SCS).Materials And Methods  This was an Institutional Review Board-approved case study involving a 37-year-old man diagnosed with CMT disease with pain of more than 20 years. He was implanted with an SCS device and patient pain and quality of life was assessed one and six months later using the SF-McGill Pain Questionnaire, Visual Analog Scale, Oswestry Disability Questionnaire, Pain Disability Index, and SF-36. Baseline measures were obtained retrospectively. Qualitative data were collected from the medical record.Results  SCS was effective in decreasing pain, improving quality of life and reducing medication consumption at both one and six months post-implant. In addition, the patient was satisfied with SCS treatment.Conclusion  SCS produced favorable results in a patient with CMT and should be considered a treatment option for pain resulting from this condition.© 2010 International Neuromodulation Society.

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