Yonsei Med J.  1999 Oct;40(5):454-459. 10.3349/ymj.1999.40.5.454.

Clinical analysis of 12 Korean Lambert-Eaton myasthenic syndrome (LEMS) patients

Affiliations
  • 1Department of Neurology, Yonsei University Wonju College of Medicine, Korea. sunwooin@yumc.yonsei.ac.kr
  • 2Department of Neurology, Yonsei University College of Medicine, Seoul, Korea.
  • 3Department of Neurology, Ulsan University Medical College, Seoul, Korea.
  • 4Department of Neurology, Wonkwang University Medical College, Seoul, Korea.
  • 5Department of Neurology, Ehwa Womans University Medical College, Seoul, Korea.

Abstract

The Lambert-Eaton myasthenic syndrome (LEMS) heralds the occurrence of malignancy, especially small-cell lung cancer (SCLC), but it can also occur in the absence of cancer. Twelve patients were diagnosed as LEMS by clinical features and the classical electrophysiological triad, which includes a low amplitude of compound muscle action potentials (CMAP), decremental responses on low-rate stimulation, and incremental responses on high-rate stimulation on the repetitive nerve stimulation (RNS) test. There were 6 male and 6 female patients, ranging in age from 49 to 66 years. Malignancy(all were SCLC) was found in 7 patients. Males predominantly expressed the paraneoplastic form; whereas the primary autoimmune form was found only in women, who showed a good response to corticosteroid treatment. The neurological features were similar in both groups: proximal lower limb weakness, depressed muscle stretch reflexes, and dryness of mouth in nearly all patients. Bulbar dysfunction and limb paresthesia were a little more frequent in the paraneoplastic form. In RNS tests, the characteristic electrophysiological abnormalities were found in all patients and were more profound in the paraneoplastic form. We concluded that LEMS is commonly associated with malignancy, especially SCLC, but it should also be stressed that there are many female LEMS patients who do not harbor any malignancy at all, and that other treatment strategies such as immunotherapy should be considered for these patients.

Keyword

Lambert-Eaton myasthenic syndrome; malignancy; small cell lung cancer; electrophysiological study; paraneoplastic; autoimmune

MeSH Terms

Aged
Carcinoma, Small Cell/complications
Female
Human
Lambert-Eaton Myasthenic Syndrome/therapy
Lambert-Eaton Myasthenic Syndrome/physiopathology*
Lung Neoplasms/complications
Male
Middle Age
Paraneoplastic Syndromes/physiopathology

Cited by  2 articles

A Case of Lambert-Eaton Myasthenic Syndrome Associated with Atypical Bronchopulmonary Carcinoid Tumor
Jae-Hyeok Lee, Jin-Hong Shin, Dae-Seong Kim, Dae Soo Jung, Kyu-Hyun Park, Min-Ki Lee, Jee-Yeon Kim
J Korean Med Sci. 2004;19(5):753-755.    doi: 10.3346/jkms.2004.19.5.753.

Clinical and Electrophysiologic Responses to Acetylcholinesterase Inhibitors in MuSK-Antibody-Positive Myasthenia Gravis: Evidence for Cholinergic Neuromuscular Hyperactivity
Ha Young Shin, Hyung Jun Park, Hyo Eun Lee, Young-Chul Choi, Seung Min Kim
J Clin Neurol. 2014;10(2):119-124.    doi: 10.3988/jcn.2014.10.2.119.

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