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Reduplicative paramnesia in Morvan's syndrome
Lynsee A Hudson1, Yvonne D Rollins, C Alan Anderson
1Department of Neurology, University of Colorado School of Medicine, Denver, Colorado, USA.
Background:
Morvan's syndrome is characterized by peripheral nervous system hyperexcitibility (myokymia and neuromyotonia), hyperhydrosis, sleep disorder, limb paresthesias, and encephalopathy. Voltage gated potassium channel antibodies (VGKC abs) are frequently present. Reduplicative paramnesia (RP) has not been reported with this disorder.
Objective:
To describe a patient with Morvan's syndrome presenting with RP.
Design:
Single case study.
Patient:
A 64-year-old man with several years of myokymia and myoclonus with escalating parasomnia and confusion developed the delusion that a replica of his house and its contents existed 40 mi away.
Results:
Serum VGKC ab titer was elevated. Neuropsychological testing disclosed executive function and memory deficits. Electromyography demonstrated diffuse myokymia. Treatment with intravenous immunoglobulin and prednisone produced improvement of RP and myoclonus, but not myokymia.
Conclusion:
RP may occur in patients with VGKC ab-associated Morvan's syndrome. Both RP and nervous system hyperexcitability may respond to immunotherapy including intravenous immunoglobulin and corticosteroids.
Insights
Reduplicative paramnesia (RP) can occur in Morvan's syndrome associated with voltage-gated potassium channel antibodies (VGKC abs). Immunotherapy, including IV immunoglobulin and corticosteroids, may improve RP and nervous system hyperexcitability.
Area of Science:
- Neurology
- Immunology
Background:
- Morvan's syndrome involves peripheral nervous system hyperexcitability, including myokymia and neuromyotonia, often associated with VGKC abs.
- Symptoms include hyperhydrosis, sleep disturbances, paresthesias, and encephalopathy.
- Reduplicative paramnesia (RP) has not been previously reported in this condition.
Observation:
- A 64-year-old male presented with a history of myokymia and myoclonus.
- He experienced worsening parasomnia and confusion, developing a delusion of a duplicate home.
- This presentation marked the first reported case of RP in Morvan's syndrome.
Findings:
- Elevated serum VGKC antibody titers were detected.
- Neuropsychological tests revealed executive function and memory deficits.
- Electromyography confirmed diffuse myokymia. Treatment with IV immunoglobulin and prednisone improved RP and myoclonus, but not myokymia.
Implications:
- RP is a potential neuropsychiatric manifestation of VGKC ab-associated Morvan's syndrome.
- Both RP and nervous system hyperexcitability may respond to immunotherapy.
- This case expands the understanding of Morvan's syndrome's clinical spectrum and treatment responses.
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