Journal
CLINICAL NEUROLOGY AND NEUROSURGERY
Volume 234, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.clineuro.2023.107994
Keywords
Anti-CASPR2; Limbic encephalitis; Morvan syndrome; Dysautonomia; Movement disorders; Neuroimmunology
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Anti-CASPR2-associated neurological disorders can manifest with isolated atypical phenotypes, a slowly progressive clinical course, and normal CSF or imaging findings.
Introduction: Anti-contactin-associated protein-like 2 (CASPR2) is classically associated with limbic encephalitis (LE), Morvan syndrome and peripheral nerve hyperexcitability (PNH). Additional clinical features have been previously recognized.Objective: To describe a cohort of patients with anti-CASPR2-associated neurological syndromes from a tertiary referral centre. Methods: Retrospective analysis of patients with positive serum anti-CASPR2 antibodies in the period between 2014 and 2021. Results: Nineteen patients were identified, 11 (57.9%) male, with a median age at symptom onset of 49.0 (31.3-63.0) years and a median time to diagnosis of 1.0 (0.0-1.8) years. The most common clinical syndromes were LE (7 cases, 36.8%), Morvan syndrome (4, 21.1%) and PNH (2, 10.5%). Six patients presented with atypical phenotypes (31.6%), comprising dysautonomia (orthostatic hypotension and Adie's Pupil), motor tics/stereotypies, obsessive-compulsive disorder, and brainstem involvement. The most common presenting symptoms were seizures (31.6%), PNH (21.1%) and cognitive dysfunction (15.8%). One LE patient had a disease duration of 2,5 years and was initially diagnosed with dementia. CSF was normal in most cases. Brain MRI showed temporal lobe hyperintensities in 4 LE cases (57.1%). All PNH cases had myokymic discharges of fasciculations in the electromyography. Two patients had associated thymoma and 1 had lung adenocarcinoma. Eight patients (42.1%) received treatment during the acute phase and 26.3% maintenance treatment. Approximately half of the treated cases improved or stabilised, with 4 (21.1%) deaths in the whole cohort. Conclusion: Anti-CASPR2-associated neurological disorders may present with isolated atypical phenotypes, a slowly progressive clinical course, and with normal CSF or imaging findings.
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