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The association between Lambert–Eaton myasthenic syndrome and small cell lung carcinoma

Lambert–Eaton myasthenic syndrome (LEMS) is an autoimmune disorder mediated by autoantibodies to voltage-gated calcium channels. The disorder is diagnosed clinically on the basis of a triad of symptoms (proximal muscle weakness, hyporeflexia, and autonomic disturbance), supported by electrophysiolog...

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Detalles Bibliográficos
Autores principales: Briggs, Sarah EW, Gozzard, Paul, Talbot, Denis C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928366/
https://www.ncbi.nlm.nih.gov/pubmed/27471686
http://dx.doi.org/10.2147/ITT.S31971
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author Briggs, Sarah EW
Gozzard, Paul
Talbot, Denis C
author_facet Briggs, Sarah EW
Gozzard, Paul
Talbot, Denis C
author_sort Briggs, Sarah EW
collection PubMed
description Lambert–Eaton myasthenic syndrome (LEMS) is an autoimmune disorder mediated by autoantibodies to voltage-gated calcium channels. The disorder is diagnosed clinically on the basis of a triad of symptoms (proximal muscle weakness, hyporeflexia, and autonomic disturbance), supported by electrophysiological findings and the presence of autoantibodies. Between 40% and 62% of patients diagnosed with LEMS are found to have small-cell lung cancer (SCLC), almost all of whom develop neurological symptoms before their cancer is diagnosed. Prompt identification of LEMS and appropriate screening for SCLC is key to improving the outcome of both conditions. Here we review the pathophysiology and clinical management of LEMS, focusing particularly on the relationship with SCLC.
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spelling pubmed-49283662016-07-28 The association between Lambert–Eaton myasthenic syndrome and small cell lung carcinoma Briggs, Sarah EW Gozzard, Paul Talbot, Denis C Immunotargets Ther Review Lambert–Eaton myasthenic syndrome (LEMS) is an autoimmune disorder mediated by autoantibodies to voltage-gated calcium channels. The disorder is diagnosed clinically on the basis of a triad of symptoms (proximal muscle weakness, hyporeflexia, and autonomic disturbance), supported by electrophysiological findings and the presence of autoantibodies. Between 40% and 62% of patients diagnosed with LEMS are found to have small-cell lung cancer (SCLC), almost all of whom develop neurological symptoms before their cancer is diagnosed. Prompt identification of LEMS and appropriate screening for SCLC is key to improving the outcome of both conditions. Here we review the pathophysiology and clinical management of LEMS, focusing particularly on the relationship with SCLC. Dove Medical Press 2013-05-21 /pmc/articles/PMC4928366/ /pubmed/27471686 http://dx.doi.org/10.2147/ITT.S31971 Text en © 2013 Briggs et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Briggs, Sarah EW
Gozzard, Paul
Talbot, Denis C
The association between Lambert–Eaton myasthenic syndrome and small cell lung carcinoma
title The association between Lambert–Eaton myasthenic syndrome and small cell lung carcinoma
title_full The association between Lambert–Eaton myasthenic syndrome and small cell lung carcinoma
title_fullStr The association between Lambert–Eaton myasthenic syndrome and small cell lung carcinoma
title_full_unstemmed The association between Lambert–Eaton myasthenic syndrome and small cell lung carcinoma
title_short The association between Lambert–Eaton myasthenic syndrome and small cell lung carcinoma
title_sort association between lambert–eaton myasthenic syndrome and small cell lung carcinoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928366/
https://www.ncbi.nlm.nih.gov/pubmed/27471686
http://dx.doi.org/10.2147/ITT.S31971
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