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DOI 10.1016/j.clinph.2005.07.016

Медицинская библиотека · Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2005

Pain and calf hypertrophy associated with spontaneous repetitive discharges treated with botulinum toxin.

Costa João, Graça Pedro, Evangelista Teresinha, de Carvalho Mamede

Клинический случайСтатьяПеревод в очереди

Аннотация

OBJECTIVE

To report a case of neurogenic calf hypertrophy associated with root lesion responsive to botulinum toxin (BTX). In addition, we systematically review the literature for cases of muscle hypertrophy associated with radiculopathy.

METHODS

A 56-year-old man with a previous history of S1 root lesion presented with marked calf hypertrophy, muscle pain, cramps, fasciculations, and increased CK level. Magnetic resonance imaging and muscle biopsy confirmed true muscle hypertrophy. Electromyography (EMG) showed signs of chronic denervation-reinnervation in the right S1 myotome, with greatly increased spontaneous activity (SA) (fasciculations and complex repetitive discharges). Botox(R) was injected in 3 occasions on 4 sites on the right gastrocnemius (20U per site). Symptoms, CK level and SA on EMG (quantified) were evaluated.

RESULTS

The patient improved clinically, CK level and SA steadily decreased.

CONCLUSIONS

The literature review failed to identify a unique causative factor for muscle hypertrophy related to neurogenic lesions. BTX treatment was effective in our patient with muscle hypertrophy associated with SA.

SIGNIFICANCE: We provide further evidence that spontaneous activity secondary to nerve lesion may cause focal muscle hypertrophy. Treatment with BTX should be considered in these conditions.

Для цитирования: Costa João, Graça Pedro, Evangelista Teresinha, de Carvalho Mamede. Pain and calf hypertrophy associated with spontaneous repetitive discharges treated with botulinum toxin.. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 2005. DOI: 10.1016/j.clinph.2005.07.016.

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