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A Case of Lambert-Eaton Myasthenic Syndrome with Small-Cell Lung Cancer and Transient Increase in Anti-Acetylcholine-Receptor-Binding Antibody Titer
Journal of Clinical Neurology ; : 305-307, 2012.
Artigo em Inglês | WPRIM | ID: wpr-12699
ABSTRACT

BACKGROUND:

Lambert-Eaton myasthenic syndrome (LEMS) is a presynaptic neuromuscular junction disorder that is most frequently associated with small-cell lung cancer (SCLC). The titers of antibodies against voltage-gated calcium channels are frequently increased in LEMS, but only rarely is titer of anti-acetylcholine-receptor-binding antibodies (AChR-abs) increased. CASE REPORT A 57-year-old male was admitted to our hospital due to dry mouth and eyes and progressive proximal limb weakness of 2 months duration. The results of a repetitive nerve stimulation test disclosed all criteria for the electrophysiological LEMS pattern, and the patient's AChR-abs titer was 0.587 nmol/L. At a follow-up performed 5 years after successful treatment of SCLC and LEMS, his AChR-abs titer had decreased to 0.001 nmol/L.

CONCLUSIONS:

We suggest that this was a case of transient pseudopositivity of AChR-abs in SCLC with LEMS.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Canais de Cálcio / Síndrome Miastênica de Lambert-Eaton / Seguimentos / Doenças da Junção Neuromuscular / Extremidades / Olho / Pulmão / Neoplasias Pulmonares / Anticorpos / Boca Tipo de estudo: Estudo observacional / Estudo prognóstico / Fatores de risco Limite: Humanos / Masculino Idioma: Inglês Revista: Journal of Clinical Neurology Ano de publicação: 2012 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Canais de Cálcio / Síndrome Miastênica de Lambert-Eaton / Seguimentos / Doenças da Junção Neuromuscular / Extremidades / Olho / Pulmão / Neoplasias Pulmonares / Anticorpos / Boca Tipo de estudo: Estudo observacional / Estudo prognóstico / Fatores de risco Limite: Humanos / Masculino Idioma: Inglês Revista: Journal of Clinical Neurology Ano de publicação: 2012 Tipo de documento: Artigo