[Lambert-Eaton myasthenic syndrome]
- PMID: 21747145
[Lambert-Eaton myasthenic syndrome]
Abstract
Lambert-Eaton myasthenic syndrome (LEMS) is an autoimmune disease of the neuromuscular junction, and approximately 60% of patients with LEMS have a tumor, mostly small cell lung cancer (SCLC), as a paraneoplastic neurological syndrome. The clinical data of Japanese patients in the present study are as follows: the ratio of men to women is 3: 1 (mean age, 62 years; age range, 17-80 years). Of the patients with LEMS, 61% have SCLC, whereas the others do not have cancer. Clinical symptoms are usually characterized by proximal muscle weakness and dysautonomia. In less than 10% of the patients, there are signs of cerebellar dysfunctions (paraneoplastic cerebellar degeneration with LEMS; PCD-LEMS), and these are usually associated with SCLC. The diagnosis can be confirmed by detecting a specific antibody in a radioimmunoprecipitation assay and finding reduced amplitude of compound muscle action potential that increases by over 100% after maximum voluntary activation or 50Hz of nerve stimulation. The pathomechanism of LEMS is characterized by impaired transmission across the neuromuscular junction because of autoantibodies directed against the presynaptic P/Q-type voltage-gated calcium channels (P/Q-VGCCs). Histopathologic evaluation of the cerebellum in patients with PCD-LEMS showed a reduced number of P/Q-type VGCCs in the molecular layer. Therefore, it was hypothesized that P/Q-VGCC antibodies may induce cerebellar dysfunction after entering the CNS in patients with PCD-LEMS. Specific tumor therapy in patients with LEMS as well as cancer often improves the neurologic deficit. Tumor removal is the primary treatment for LEMS. If the result of the primary screening is negative, screening should be repeated after 3-6 months and thereafter every 6 months for up to 2 years. Most patients benefit from 3, 4-diaminopyridine administered with pyridostigmine. In those with severe weakness, intravenous gamma globulin (IVIg) or plasmapheresis confers short-term benefits. Prednisone when administered alone or in combination with immunosuppressive drugs can achieve long-term control of the disorder.
Similar articles
-
[P/Q-type Calcium Channel Antibodies in Lambert-Eaton Myasthenic Syndrome].Brain Nerve. 2018 Apr;70(4):341-355. doi: 10.11477/mf.1416201007. Brain Nerve. 2018. PMID: 29632282 Japanese.
-
[Autoantibody against the presynaptic P/Q-type voltage-gated calcium channel in Lambert-Eaton myasthenic syndrome].Brain Nerve. 2013 Apr;65(4):441-8. Brain Nerve. 2013. PMID: 23568992 Review. Japanese.
-
Reduction of P/Q-type calcium channels in the postmortem cerebellum of paraneoplastic cerebellar degeneration with Lambert-Eaton myasthenic syndrome.Ann Neurol. 2003 Jan;53(1):21-8. doi: 10.1002/ana.10392. Ann Neurol. 2003. PMID: 12509844
-
[Paraneoplastic cerebellar degeneration and Lambert-Eaton myasthenic syndrome associated with anti P/Q-type voltage-gated calcium channel antibody in a patient with primary double lung cancer].Brain Nerve. 2009 Sep;61(9):1083-7. Brain Nerve. 2009. PMID: 19803409 Japanese.
-
Lambert-Eaton myasthenic syndrome.Rev Neurol (Paris). 2004 Feb;160(2):177-80. doi: 10.1016/s0035-3787(04)70888-7. Rev Neurol (Paris). 2004. PMID: 15034474 Review.
Cited by
-
Lung adenocarcinoma with Lambert-Eaton myasthenic syndrome indicated by voltage-gated calcium channel: a case report.J Med Case Rep. 2012 Sep 5;6:281. doi: 10.1186/1752-1947-6-281. J Med Case Rep. 2012. PMID: 22950670 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources