| Literature DB >> 28781798 |
Yoshiya Tsunoda1, Takumi Kiwamoto1, Shinsuke Homma1, Yuuki Yabuuchi1, Haruna Kitazawa1, Toshihiro Shiozawa1, Kensuke Nakazawa1, Takashi Hosaka2, Kazuhiro Ishii2, Akiko Ishii2, Akira Tamaoka2, Nobuyuki Hizawa1.
Abstract
Paraneoplastic limbic encephalitis (PLE), a paraneoplastic neurological syndrome (PNS), is a rare nervous system disorder that results from the indirect effects of tumors and is commonly associated with small-cell lung cancer (SCLC). Previous studies have reported that magnetic resonance imaging (MRI) may be useful for diagnosing LE. Temporal lobe abnormalities are observed using T2-weighted and fluid-attenuated inversion recovery sequences; however, such abnormalities are detected in only 60% of patients with PLE. The present study describes a case of PLE associated with SCLC, in which LE was observed using MRI 26 days after the first convulsive seizure. Although the serum and cerebrospinal fluid analyses for onconeural antibodies were negative, the findings of this case indicate that PLE should be considered in the differential diagnosis, and that repeated brain MRI may be more helpful for diagnosis, as the brain MRI findings may be normal during the early stages of PLE.Entities:
Keywords: magnetic resonance imaging; onconeural antibody; paraneoplastic limbic encephalitis; paraneoplastic neurological syndromes; small-cell lung cancer
Year: 2017 PMID: 28781798 PMCID: PMC5532705 DOI: 10.3892/mco.2017.1311
Source DB: PubMed Journal: Mol Clin Oncol ISSN: 2049-9450