Archives of Neurology · 2012 · 59 citations · 8 references
MedicineNeurologyNeuroscienceNeuroimmunologyNeuromuscular DisordersNeuropathologyDemyelinating DiseasesDemyelinating DisordersMultiple SclerosisOptic NeuritisInstitutional Review Board ApprovalInternational Classification Of DiseasesMedian AgeNeuromyelitis Optica Spectrum Disorder-associated Optic NeuritisRadiographic ClassificationRetrospective Case Study
OBJECTIVE: To determine the frequency of the association between tonic spasms and neuromyelitis optica (NMO) at our center. DESIGN: An institutional review board-approved retrospective study of clinical, serological, and radiographic characteristics of patients with NMO. SETTING: Multiple sclerosis center. PATIENTS: Patients with NMO treated at our center between 1990 and 2008. MAIN OUTCOME MEASURE: Records were examined for documentation of tonic spasms. RESULTS: Of 110 patients with International Classification of Diseases code 341, 57 patients met diagnostic criteria for NMO. Of these, 8 patients (14%) had documented typical tonic spasms (median age at onset, 39.5 years; range, 13.8-54.2 years). Of those patients, 4 were African American, 3 were Hispanic, and 1 was white. Only 1 was male. The NMO-IgG antibody was found in 1 of 6 patients tested. Tonic spasms appeared after a mean of 24.6 months (range, 0-91 months). In 2 of 57 patients meeting NMO criteria, tonic spasms accompanied their initial episodes. Seven of 8 patients who had tonic spasms responded to treatment with carbamazepine within 1 week. CONCLUSION: Tonic spasms are associated with NMO more commonly than with multiple sclerosis and may be a presenting sign in both diseases.
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Revised diagnostic criteria for neuromyelitis optica
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