Case Reports in Neurological Medicine

Volume 2013 (2013), Article ID 369278, 2 pages

http://dx.doi.org/10.1155/2013/369278

Case Report

Pseudomyopathic Changes in Needle Electromyography in Lambert-Eaton Myasthenic Syndrome

Teppei Komatsu,1,2 Kota Bokuda,¹ Toshio Shimizu,¹ Tetsuo Komori,³ and Reiji Koide¹

¹Department of Neurology, Tokyo Metropolitan Neurological Hospital, 2-6-1 Musashidai, Fuchu, Tokyo 183-0042, Japan

²Department of Neurology, The Jikei University School of Medicine, Japan

³Department of Neurology, National Hakone Hospital, Japan

Received 12 June 2013; Accepted 4 July 2013

Academic Editors: S. T. Gontkovsky and Z. Siddiqi

Copyright © 2013 Teppei Komatsu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Lambert-Eaton myasthenic syndrome (LEMS) is a rare presynaptic disorder of the neuromuscular junction in association with cancer and subsequently in cases in which no neoplasm has been detected (O’Neill et al., 1988). The diagnosis of LEMS is based on the combination of fluctuating muscle weakness, diminished or absent reflexes, and a more than 60% increment of compound muscle action potential (CMAP) amplitude after brief exercise or 50 Hz stimulation for 1 s in a repetitive nerve stimulation (RNS) test (Oh et al., 2005). On the other hand, needle electromyography (EMG) findings related to LEMS have not been well described. Here, we report a case of LEMS, which showed apparent myopathic changes in needle EMG findings. Furthermore, we retrospectively examined the needle EMG findings in 8 patients with LEMS. In six of the 8 patients, the EMG findings showed myopathy-like findings. Although the findings of needle EMG indicated myopathic changes at a glance, the motor unit potential (MUP) returned to normal after a sustained strong muscle contraction. We propose the name “pseudomyopathic changes” for this phenomenon.

1. Case Report

A 69-year-old female (patient 1 in Table 1) developed a gait disturbance 6 months before admission and suffered from the gradual progression of weakness in her extremities. On admission, neurological examination showed proximal muscle weakness and reduced deep tendon reflex. Routine laboratory test results were unremarkable. Antinuclear antibodies, anti-acetylcholine (ACh) receptor antibody, and anti-voltage-gated calcium channel (VGCC) antibodies were negative. The results of chest and abdominal CT were unremarkable. In a nerve conduction study, CMAPs had slightly low amplitudes, and nerve conduction velocities were normal in the median and ulnar nerves. Needle EMG showed early recruitment and polyphasic MUPs with short durations and low amplitudes, suggesting the diagnosis of myopathy. Interestingly, the myopathic EMG findings were improved after sustained strong muscle contraction for 10 s; the MUP sizes returned to normal after a sustained strong muscle contraction, and the early recruitment of MUPs in the weak contraction was clearly normalized in the biceps brachii muscle (Figure 1). Thereafter, we performed an RNS test because she complained of easy fatigability. The RNS test showed an obvious incremental response of the CMAP amplitude of the abductor digiti minimi muscle after high-rate stimulation of the ulnar nerve, indicating the diagnosis of LEMS [1–3]. We examined the patient for systemic malignancies, and the endoscopic examination of the colon revealed adenocarcinoma in the sigmoid colon. Her muscle weakness slightly improved after resection of the colon cancer.

Table 1: Characteristics of patients.

Patient
Sex
Age
Needle EMG
RNS
Neoplasm
Anti-VGCC antibody

1
F
69
Pseudomyopathic
Increased
Colon adenocarcinoma
Negative

2
M
70
Pseudomyopathic
Increased
SCLC
Positive

3
F
72
Pseudomyopathic
Increased
SCLC
Positive

4
M
71
Pseudomyopathic
Increased
SCLC
Positive

5
M
49
Pseudomyopathic
Increased
Unknown
Positive

6
M
67
Pseudomyopathic
Increased
SCLC
Positive

7
F
56
Normal
Increased
SCLC
Positive

8
M
71
Normal
Increased
Unknown 　
Unknown

EMG: electromyography; RNS: repetitive nerve stimulation; SCLC: small-cell lung carcinoma; VGCC: voltage-gated calcium channel.

(a)

(b)

Figure 1: Needle EMG findings in patient 1. The MUPs (arrows) with short durations and low amplitudes were observed in the biceps brachii muscle (a). After a strong muscle contraction for 10 s, the MUP sizes were normalized (b).

2. Discussion

We retrospectively analyzed the needle EMG findings in the 8 patients with LEMS (Table 1). All patients were hospitalized in our hospital between June 1997 and August 2012. The mean age was 66 years (range from 49 to 72). Malignant tumors were detected in six of the 8 patients, of whom five had small-cell lung cancer (SCLC) and one had colon adenocarcinoma. Anti-VGCC antibodies were detected in all five patients with LEMS associated with SCLC. Incremental responses in the RNS test were observed in all patients. In six of the 8 patients, myopathy-like findings similar to the present case were found by needle EMG, characterized by initial myopathic patterns and normalization of the recruitments and MUP amplitude after a strong muscle contraction. We propose the name “pseudomyopathic changes” for this phenomenon.

LEMS is typically caused by pathogenic autoantibodies to the presynaptic VGCCs in the membrane of motor nerve terminals, inducing the impairment of ACh release [2, 4]. Mechanism of abnormalities in the needle EMG of LEMS patients is presumed as follows: end-plate potential (EPP) decreases in LEMS because EPP increases in proportion to the number of Ach quanta liberated from the nerve terminal. When the EPP fails to reach excitability threshold of the muscle cell, an action potential does not ensue and a neuromuscular block results. Desynchronized discharges and the intermittent blocking of individual muscle fibers within the motor unit induce polyphasic MUP with a low amplitude, mimicking myopathic features of EMG. Normalization of the MUP amplitude and the motor unit recruitment after a strong muscle contraction is attributed to the enhancement of ACh release from the nerve terminals.

Physicians should not easily eliminate the possibility of LEMS, if myopathic features of EMG were observed in the patients with muscle weakness.

Conflict of Interests

The authors do not have a direct financial relation with the commercial identities mentioned in the paper that might lead to a conflict of interests.

Acknowledgment

The authors thank Dr. Masakatsu Motomura of the Department of Clinical Neuroscience and Neurology, Nagasaki University, for measuring the anti-VGCC antibody.

References

S. J. Oh, K. Kurokawa, G. C. Claussen, et al., “Electrophysiological diagnostic criteria of Lambert-Eaton myasthenic syndrome,” Muscle and Nerve, vol. 32, no. 4, pp. 515–520, 2005.

N. E. Gilhus, “Lambert-eaton myasthenic syndrome, pathogenesis, diagnosis, and therapy,” Autoimmune Diseases, vol. 2011, Article ID 973808, 5 pages, 2011.

M. J. Titulaer, B. Lang, and J. J. Verschuuren, “Lambert-Eaton myasthenic syndrome: from clinical characteristics to therapeutic strategies,” The Lancet Neurology, vol. 10, no. 12, pp. 1098–1107, 2011.

J. H. O'Neill, N. M. F. Murray, and J. Newsom-Davis, “The Lambert-Eaton myasthenic syndrome. A review of 50 cases,” Brain, vol. 111, no. 3, pp. 577–596, 1988.