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lüll Non-paraneoplastic Lambert-Eaton myasthenic syndrome: a brief review of 10 cases Lorenzoni PJ; Scola RH; Kay CS; Parolin SF; Werneck LCArq Neuropsiquiatr 2010[Dec]; 68 (6): 849-54Lambert-Eaton myasthenic syndrome (LEMS) is an immune-mediated disorder of the presynaptic neuromuscular transmission, which more frequently occurs as the remote effect of a neoplasm, in the paraneoplastic form (P-LEMS), or in a non-paraneoplastic form (NP-LEMS); but few studies describe the clinical features of NP-LEMS. We analyzed the clinical manifestations, laboratory findings, electrophysiological studies, and treatment responses in ten Brazilian patients suffering from NP-LEMS. The mean age was 41.5 years. More often neurological findings were hyporeflexia or areflexia with a post-exercise improvement. Treatment response occurred with pyridostigmine, guanidine, prednisone, azathioprine, and cyclosporine; but not response was observed after intravenous immunoglobulin and plasma exchange. Age at onset, clinical manifestations, and electrophysiological abnormalities can help more in the diagnosis than serum antibodies; the symptomatic treatment with pyridostigmine was effective; and the immunosuppressive treatment with prednisone, azathioprine, or cyclosporine was more beneficial than plasma exchange or intravenous immunoglobulin treatment.|*Lambert-Eaton Myasthenic Syndrome/diagnosis/physiopathology/therapy[MESH]|Adult[MESH]|Electrophysiology[MESH]|Female[MESH]|Humans[MESH]|Immunoglobulins, Intravenous/therapeutic use[MESH]|Immunosuppressive Agents/therapeutic use[MESH]|Male[MESH]|Middle Aged[MESH]|Plasmapheresis[MESH]|Retrospective Studies[MESH] |