- Case report
- Open Access
- Open Peer Review
Lung adenocarcinoma with Lambert–Eaton myasthenic syndrome indicated by voltage-gated calcium channel: a case report
© Arai et al.; licensee BioMed Central Ltd. 2012
- Received: 19 April 2012
- Accepted: 26 June 2012
- Published: 5 September 2012
Lambert–Eaton myasthenic syndrome is a rare disorder and it is known as a paraneoplastic neurological syndrome. Small cell lung cancer often accompanies this syndrome. Lambert–Eaton myasthenic syndrome associated with lung adenocarcinoma is extremely rare; there are only a few reported cases worldwide.
A 75-year-old Japanese man with a past history of chronic rheumatoid arthritis and Sjögren syndrome was diagnosed with Lambert–Eaton myasthenic syndrome by electromyography and serum anti-P/Q-type voltage-gated calcium channel antibody level preceding the diagnosis of lung cancer. A chest computed tomography to screen for malignant lesions revealed an abnormal shadow in the lung. Although a histopathological examination by bronchoscopic study could not reveal the malignancy, lung cancer was mostly suspected after the results of a chest computed tomography and [18F]-fluorodeoxyglucose positron emission tomography. An intraoperative diagnosis based on the frozen section obtained by tumor biopsy was adenocarcinoma so the patient underwent a lobectomy of the right lower lobe and lymph node dissection with video-assisted thoracoscopic surgery. The permanent pathological examination was the same as the frozen diagnosis (pT2aN1M0: Stage IIa: TNM staging 7th edition). Immunohistochemistry revealed that most of the cancer cells were positive for P/Q-type voltage-gated calcium channel.
Our case is a rare combination of Lambert–Eaton myasthenic syndrome associated with lung adenocarcinoma, rheumatoid arthritis and Sjögren syndrome, and to the best of our knowledge it is the first report that indicates the presence of voltage-gated calcium channel in lung adenocarcinoma by immunostaining.
- Lambert–Eaton myasthenic syndrome
- Lung adenocarcinoma
- Voltage-gated calcium channel
Lambert–Eaton myasthenic syndrome (LEMS) is a rare but well-known paraneoplastic disorder characterized by muscle weakness and fatigability predominantly involving the proximal lower limbs. Recently, measurement of serum anti-P/Q-type voltage-gated calcium channel (VGCC) antibody level has been used, in addition to clinical manifestations and nerve conduction studies, to diagnose LEMS. Patients with LEMS have mostly small cell lung cancer (SCLC); other subtypes of lung cancer are extremely rare. We present a rare case of LEMS associated with pulmonary adenocarcinoma, chronic rheumatoid arthritis (RA) and Sjögren syndrome (Sjs) and provide findings of the resected specimen immunostained with P/Q-type VGCC.
The patient had worked as a carpenter before the onset of muscle weakness. However, as his symptoms worsened, he required assistance in daily life (performance status 2). He was admitted to our ward by wheelchair. He had a history of chronic RA medicated by oral prednisolone therapy. He also complained of thirst for many months. A full blood examination and biochemical examination were almost within the normal range. Carcinoembryonic antigen was slightly elevated to 6.0ng/mL, whereas other tumor markers for lung cancer (squamous cell carcinoma-related antigen, sialylated Lewis X-i antigen, cytokeratin fragment, neuron-specific enolase and progastrin-releasing peptide) were within normal ranges. On screening for autoimmune disease and collagen disease, serum CH50 was slightly elevated to 46.7U/mL (normal range, 30 to 45), and rheumatoid factor was within the normal range (10.4IU/mL; normal range, 0 to 20). On screening for other collagen diseases, anti-nuclear antibody was positive at the titer of 1:640 and anti-SSA/Ro antibody was elevated to >500U/mL (normal range, 0–100). At this time it was clear that the patient also had Sjs. He had a history of cigarette smoking (40 cigarettes per day for 40 years). The preoperative spirometry result was, %VC: 63.9% and FEV1.0% 76.0%; and the blood gas analysis result was pCO2 38.9mmHg and pO2 83.1mmHg (room air).
An operation was performed for a definite diagnosis and treatment of the tumor. An intraoperative frozen diagnosis obtained by tumor biopsy revealed lung adenocarcinoma, and he underwent right lower lobe lobectomy and lymph node dissection with video-assisted thoracoscopic surgery. The operation took 230 minutes, with a blood loss of 200mL. In the postoperative course, because of prolonged air leakage from the remaining right pulmonary lobes, tube drainage lasted for 9 days. Muscle weakness gradually improved on approximately postoperative day 5, and he could walk without assistance. Serum P/Q-type VGCC antibody level was still elevated to 30.6pmol/L on postoperative day 7. He underwent daily rehabilitation for discharge. Approximately 2 months after the operation, he had aspiration pneumonia with respiratory failure. Intubation and respiratory management were performed in the intensive care unit. He remains ventilator dependent at 4 months postoperation. Postoperative provocative nerve conduction studies could not be performed.
LEMS is one of the representative paraneoplastic syndromes and an autoimmune disease of the neuromuscular junction. Because of its scarcity, the exact incidence of LEMS is unknown. The prevalence of as few as 400 cases in the USA in 1994 and of 2 to 3 cases per million inhabitants in the Netherlands in 2004 has been reported.
LEMS is also thought to be a complication of organ-specific autoimmune diseases, such as thyroid disease, vitiligo, pernicious anemia, coeliac disease, and juvenile-onset diabetes mellitus. However, systemic lupus erythematosus, Sjs and RA associated with LEMS is rare; only a few cases are reported in the English literature[4, 8].
Clinical manifestation of LEMS is usually characterized by proximal muscle weakness affecting the legs more than the arms, fatigability and dysautonomia. Malignant neoplasm usually occurs within the first 2 years after the onset of LEMS and in almost all patients after 4 years. Therefore, once LEMS is diagnosed or strongly suspected, screening for malignant neoplasm, especially SCLC (for example, using chest CT or tumor markers: neuron-specific enolase and progastrin-releasing peptide), is recommended. Moreover, careful observation and screening should be required for at least 2 years[4–6]. The treatment of SCLC controls its mortality and often results in normalization of both electrodiagnostic findings and clinical symptoms of LEMS[5, 6].
The diagnosis of LEMS is established by clinical manifestation and by characteristic findings on nerve conduction studies. The nerve conduction study findings indicate reduced amplitude of compound muscle action potential that increases by over 100% after maximum voluntary activation or 20 to 50Hz of nerve stimulation, and incremental response (waxing) of compound muscle action potential on the rapid rate of repetitive stimulation[5, 6].
In the 1990s, Motomura and co-workers established a new immunoassay of antibodies to VGCC for the diagnosis of LEMS. VGCCs are situated on the presynaptic nerve terminal and have a central role in the control of neurotransmitter release[1, 9]. Antibodies to VGCC inhibit transmitter (acetylcholine) release at presynaptic nerve terminals. It has been assumed that SCLC expresses functional calcium channels and that autoantibodies to these channels may cross-react with similar VGCCs[1, 5, 6, 9]. Motomura reported 85% of patients with LEMS to be positive for VGCC and suggests that the titer of anti-P/Q-type VGCC antibody in particular occupies an important position in the diagnosis of LEMS; the remaining 15% of patients were seronegative for VGCC. In this subgroup, SCLC is less common and the exact explanation of seronegative LEMS is still unknown. Thus, a negative antibody titer of VGCC is not necessarily an indicator of the absence of LEMS.
Characteristics of patients with Lambert–Eaton myasthenic syndrome associated with lung adenocarcinoma
Coexistent collagen disease
Death at 2 years
(due to infection)
Surviving at 2 years
Death at 5 months
(due to DIC)
Death at 16 days
(due to sepsis)
This case report
Surviving at 4 months
We examined P/Q-type VGCC expression immunohistochemically using resected lung tumor sections. Most of the neoplastic cells were stained positive, and the area consisting of poorly-differentiated neoplastic cells tended to show stronger signals. As far as we know, no report has demonstrated immunohistochemical expression of VGCC in neoplastic cells.
Taking together the results of immunostaining and the fact that our patient also had collagen diseases (RA and Sjs), autoimmune function may be related to the onset of LEMS and, in the case of lung adenocarcinoma, lower-differentiated cases appear to develop P/Q-type VGCC. However, the actual mechanism by which anti-P/Q-type VGCC antibody causes LEMS is unclear because the experimental model of this rare disease has not been established. Further molecular biological studies are required. Clinically, physicians must manage patients with muscle weakness while considering LEMS as a differential diagnosis. Recognition and awareness of this rare syndrome are essential for a better prognosis and quality of life for these patients.
Written informed consent was obtained from the patient of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
We are grateful to Dr. Masakatsu Motomura (Department of Clinical Neuroscience and Neurology Graduate School of Biomedical Science, Nagasaki University) for analyzing the serum levels of the anti-P/Q-type VGCC antibody titer and useful discussion.
- Motomura M, Johnston I, Lang B, Vincent A, Newsom-Davis J: An improved diagnostic assay for Lambert-Eaton myasthenic syndrome. J Neurol Neurosurg Psychiatry. 1995, 58: 85-87. 10.1136/jnnp.58.1.85.View ArticlePubMedPubMed CentralGoogle Scholar
- McEvoy KM: Diagnosis and treatment of Lambert-Eaton myasthenic syndrome. Neurol Clin. 1994, 12: 387-399.PubMedGoogle Scholar
- Wirtz PW, van Dijk JG, van Doorn PA, van Engelen BGM, van der Kooi AJ, Kuks JB, Twijnstra A, de Visser M, Visser LH, Wokke JH, Wintzen AR, Verschuuren JJ: The epidemiology of the Lambert-Eaton myasthenic syndrome in the Netherlands. Neurology. 2004, 63: 397-398. 10.1212/01.WNL.0000130254.27019.14.View ArticlePubMedGoogle Scholar
- O’neill JH, Murray NMF, Newsom-Davis J: The Lambert-Eaton myasthenic syndrome. A review of 50 cases. Brain. 1988, 111: 577-596. 10.1093/brain/111.3.577.View ArticlePubMedGoogle Scholar
- Lin JT, Lachmann E: Lambert-Eaton myasthenic syndrome: a case report and review of the literature. J Womens Health. 2002, 11: 849-855. 10.1089/154099902762203696.View ArticleGoogle Scholar
- Motomura M, Fukuda T: Lambert-Eaton myasthenic syndrome. Brain Nerve. 2011, 63: 745-754. in Japanese with English abstractPubMedGoogle Scholar
- Ramos-Yeo YL, Reyes CV: Myasthenic syndrome (Eaton-Lambert syndrome) associated with pulmonary adenocarcinoma. J Surg Oncol. 1987, 34: 239-242. 10.1002/jso.2930340405.View ArticlePubMedGoogle Scholar
- Tsuchiya N, Sato M, Uesaka Y, Kurose N, Haida M, Nakano J, Tsuchida T, Inoue T, Ito K: Lambert-Eaton myasthenic syndrome associated with Sjögren’s syndrome and discoid lupus erythematosus. Scand J Rheumatol. 1993, 22: 302-304. 10.3109/03009749309095144.View ArticlePubMedGoogle Scholar
- Nakao YK, Motomura M, Fukudome T, Fukuda T, Shiraishi H, Yoshimura T, Tsujihata M, Eguchi K: Seronegative Lambert-Eaton myasthenic syndrome. Study of 110 Japanese patients. Neurology. 2002, 59: 1773-1775. 10.1212/01.WNL.0000037485.56217.5F.View ArticlePubMedGoogle Scholar
- Milanez FM, Pereira CAC, Trindade PHDM, Milinavicius R, Coletta ENAM: Lung adenocarcinoma, dermatomyositis, and Lambert-Eaton myasthenic syndrome: a rare combination. J Bras Pneumol. 2008, 34: 333-336. 10.1590/S1806-37132008000500014.View ArticlePubMedGoogle Scholar
- Sumitomo M, Uyama T, Kimura S, Hashioka K, Nobuhara K, Monden Y: A case of Lambert-Eaton myasthenic syndrome associated with adenocarcinoma of the lung. Haigan. 1989, 29: 167-172. 10.2482/haigan.29.167. in Japanese with English abstractView ArticleGoogle Scholar
- Okudera K, Ebina A, Imai S, Kurahashi K, Kushihiki D, Takanashi S, Okumura K: A case with adenocarcinoma of the lung accompanied Lambert-Eaton myasthenic syndrome. Nikkyo. 1996, 55: 902-907. in Japanese with English abstractGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.