Lung adenocarcinoma with Lambert-Eaton myasthenic syndrome indicated by voltage-gated calcium channel: A case report

被引:7
作者
Arai H. [1 ]
Inui K. [1 ]
Hashimoto K. [1 ]
Kan-O K. [1 ]
Nishii T. [1 ]
Kishida H. [2 ]
Okudela K. [5 ]
Tsuboi M. [1 ]
Nozawa A. [3 ]
Kaneko T. [1 ]
Masuda M. [4 ]
机构
[1] Respiratory Disease Center, Yokohama City University Medical Center, Minami-ku, Yokohama 232-0024
[2] Department of Neurology, Yokohama City University Medical Center, Minami-ku, Yokohama 232-0024
[3] Department of Pathology, Yokohama City University Medical Center, Minami-ku, Yokohama 232-0024
[4] Department of Surgery, Yokohama City University, Graduate School of Medicine, Kanazawa-ku, Yokohama 236-0004
[5] Department of Pathology, Yokohama City University, Graduate School of Medicine, Kanazawa-ku, Yokohama 236-0004
关键词
Immunostaining; Lambert-Eaton myasthenic syndrome; Lung adenocarcinoma; Voltage-gated calcium channel;
D O I
10.1186/1752-1947-6-281
中图分类号
学科分类号
摘要
Introduction. 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. Case presentation. 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. Conclusions: 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. © 2012 Arai et al.; licensee BioMed Central Ltd.
引用
收藏
相关论文
共 12 条
[1]  
Motomura M., Johnston I., Lang B., Vincent A., Newsom-Davis J., An improved diagnostic assay for Lambert-Eaton myasthenic syndrome, J Neurol Neurosurg Psychiatry, 58, pp. 85-87, (1995)
[2]  
McEvoy K.M., Diagnosis and treatment of Lambert-Eaton myasthenic syndrome, Neurol Clin, 12, pp. 387-399, (1994)
[3]  
Wirtz P.W., Van Dijk J.G., Van Doorn P.A., Van Engelen B.G.M., Van Der Kooi A.J., Kuks J.B., Twijnstra A., De Visser M., Visser L.H., Wokke J.H., Wintzen A.R., Verschuuren J.J., The epidemiology of the Lambert-Eaton myasthenic syndrome in the Netherlands, Neurology, 63, pp. 397-398, (2004)
[4]  
O'Neill J.H., Murray N.M.F., Newsom-Davis J., The Lambert-Eaton myasthenic syndrome. A review of 50 cases, Brain, 111, pp. 577-596, (1988)
[5]  
Lin J.T., Lachmann E., Lambert-Eaton myasthenic syndrome: A case report and review of the literature, J Womens Health, 11, pp. 849-855, (2002)
[6]  
Motomura M., Fukuda T., Lambert-Eaton myasthenic syndrome, Brain Nerve, 63, pp. 745-754, (2011)
[7]  
Ramos-Yeo Y.L., Reyes C.V., Myasthenic syndrome (Eaton-Lambert syndrome) associated with pulmonary adenocarcinoma, J Surg Oncol, 34, pp. 239-242, (1987)
[8]  
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, 22, pp. 302-304, (1993)
[9]  
Nakao Y.K., 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, 59, pp. 1773-1775, (2002)
[10]  
Milanez F.M., Pereira C.A.C., Trindade P., Milinavicius R., Coletta E., Lung adenocarcinoma, dermatomyositis, and Lambert-Eaton myasthenic syndrome: A rare combination, J Bras Pneumol, 34, pp. 333-336, (2008)