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An Unusual Case of Muscle Twitching: Its LGI1
Laxmikant Ramkumarsingh Tomar1, Dhrumil Jatinbhai Shah1, Rajeev Ranjan1
1Department of Neurology, Sir Ganga Ram Hospital, Old Rajendra Nagar, New Delhi, India.
Neurology India
|April 27, 2021
Summary
A patient with peripheral nerve hyperexcitability syndrome experienced symptoms like paresthesias and twitching. Treatment with immunoglobulin and carbamazepine led to significant improvement.
Area of Science:
- Neurology
- Immunology
Background:
- Peripheral nerve hyperexcitability (PNH) syndrome is a rare autoimmune disorder.
- Leucin-rich glioma-inactivated 1 (LGI1) antibodies are implicated in certain neurological conditions.
Observation:
- A 50-year-old male presented with a two-month history of ascending paresthesias and continuous body twitching, accompanied by insomnia.
- Electromyography (EMG) indicated neuromyotonia, a hallmark of peripheral nerve hyperexcitability.
Findings:
- The patient was diagnosed with LGI1 antibody-associated PNH syndrome.
- Treatment with intravenous immunoglobulin and carbamazepine resulted in significant symptom improvement.
Implications:
- This case highlights the importance of identifying LGI1 antibodies in PNH syndrome.
- Effective treatment strategies involving immunotherapy and anticonvulsants can be employed for LGI1-associated PNH.
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