Kazuki Hashimoto
Department School of Medicine(Yachiyo Medical Center), School of Medicine Position Assistant Professor |
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Article types | Original article |
Language | English |
Peer review | Peer reviewed |
Title | Lung adenocarcinoma with Lambert-Eaton myasthenic syndrome indicated by voltage-gated calcium channel: a case report. |
Journal | Formal name:Journal of medical case reports Abbreviation:J Med Case Rep ISSN code:17521947/17521947 |
Domestic / Foregin | Foregin |
Volume, Issue, Page | 6,pp.281 |
Author and coauthor | Arai Hiromasa, Inui Kenji, Hashimoto Kazuki, Kan-O Kazuki, Nishii Teppei, Kishida Hitaru, Okudela Koji, Tsuboi Masahiro, Nozawa Akinori, Kaneko Takeshi, Masuda Munetaka |
Publication date | 2012/09 |
Summary | 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. |
DOI | 10.1186/1752-1947-6-281 |
PMID | 22950670 |