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Reversible spontaneous EMG activity during myasthenic crisis: Two case reports.
Theocharis Tsironis1,2, Santiago Catania1
1Department of Clinical Neurophysiology, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK.
Eneurologicalsci
|December 18, 2018
Summary
Severe Myasthenia Gravis (MG) can present with spontaneous EMG activity, mimicking other neuromuscular disorders. This case highlights the importance of considering MG even with atypical EMG findings to ensure timely diagnosis and treatment.
Area of Science:
- Neurology
- Neurophysiology
- Autoimmune Disorders
Background:
- Myasthenia Gravis (MG) is an autoimmune neuromuscular disorder characterized by fatigable muscle weakness.
- Standard EMG findings in MG typically include decremental response and increased jitter, with spontaneous activity considered atypical.
Observation:
- Two patients with severe bulbar symptoms presented with spontaneous EMG activity.
- Initial diagnoses were inflammatory myopathy and anterior horn cell disease due to these atypical EMG findings.
Findings:
- Despite atypical EMG findings, subsequent investigations including anti-AchR antibody testing and response to treatment confirmed Myasthenia Gravis.
- This indicates that spontaneous EMG activity can occur in severe MG cases.
Implications:
- Clinically severe Myasthenia Gravis may exhibit spontaneous EMG activity, potentially mimicking other neurological conditions.
- Recognizing this atypical presentation is crucial to avoid diagnostic delays and ensure appropriate management of MG.
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