Acetylcholine receptor antibodies in the Lambert-Eaton myasthenic syndrome

J. S. Katz, G. I. Wolfe, W. W. Bryan, Ron Tintner, Richard J. Barohn

Research output: Contribution to journalArticle

34 Scopus citations

Abstract

Two patients were initially diagnosed with myasthenia gravis with elevated titers of acetylcholine receptor antibodies. Features including weakness that normalized with sustained contraction, areflexia, autonomic symptoms, and low-amplitude baseline compound muscle action potentials with abnormal increments following brief exercise and high-frequency repetitive stimulation, however, suggested that these patients had Lambert-Eaton myasthenic syndrome. One patient had antibodies directed against presynaptic calcium channels, confirming the diagnosis. The second patient was seronegative for these antibodies but had elevated titers of antistriated muscle antibodies. This shows that serologic studies can conflict with clinical and electrodiagnostic findings in patients with Lambert-Eaton syndrome. These cases also point out that acetylcholine receptor antibodies are not necessarily diagnostic of myasthenia gravis in patients with Lambert- Eaton syndrome. Instead, these antibodies could represent a nonpathogenic epiphenomenon.

Original languageEnglish (US)
Pages (from-to)470-475
Number of pages6
JournalNeurology
Volume50
Issue number2
DOIs
StatePublished - Jan 1 1998

ASJC Scopus subject areas

  • Clinical Neurology

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