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Clinical Reasoning: Adult Patient Presenting With Spine Pain Following a Motor Vehicle Accident
Vaishnavi Sharma1, Oscar Soto2
1From the Tufts University School of Medicine (V.S., O.S.); Department of Neurology (O.S.), Tufts Medical Center, Boston, MA.
A rare myopathy was diagnosed in a patient with persistent spine pain, thanks to specialized electromyography (EMG) of paraspinal muscles. This diagnostic approach is crucial for identifying treatable myopathies early.
Area of Science:
- Neurology
- Clinical Electrophysiology
- Myology
Background:
- A 52-year-old woman presented with refractory spine pain post-trauma.
- Complex medical history including consanguinity and normal initial limb EMG.
- Spine imaging showed paraspinal muscle fatty degeneration and atrophy.
Observation:
- Clinical examination lacked specific findings.
- Mildly elevated creatine phosphokinase levels were noted.
- Follow-up EMG of paraspinal and trunk muscles revealed myopathic abnormalities.
Findings:
- Electromyography (EMG) demonstrated myotonic discharges, fibrillations, positive sharp waves, and myopathic motor unit potentials in paraspinal muscles.
- These neurophysiological findings were key to diagnosing a myopathic disorder.
- The diagnostic process confirmed a rare, treatable myopathy.
Implications:
- Highlights the diagnostic value of paraspinal muscle EMG in complex pain cases.
- Emphasizes the importance of targeted neurophysiological evaluation for diagnosing myopathies.
- Facilitates early diagnosis and treatment of rare myopathies, improving patient outcomes.
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