Following sensory neuropathy, anti-Hu antibody-positive paraneoplastic neurological syndrome presenting with limbic encephalitis occurs after complete remission
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- Fukami Yuki
- Department of Neurology, Chubu Rosai Hospital
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- Umemura Toshitaka
- Department of Neurology, Chubu Rosai Hospital
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- Shimono Tetufumi
- Department of Neurology, Chubu Rosai Hospital
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- Yokoi Takamasa
- Department of Neurology, Chubu Rosai Hospital
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- Kamijo Mikiko
- Department of Neurology, Chubu Rosai Hospital
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- Sakakibara Toshimasa
- Department of Neurology, Chubu Rosai Hospital Present Address: Department of Neurology, Owari Onsen Rehabilitation Kanie Hospital
Bibliographic Information
- Other Title
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- 感覚性ニューロパチーが先行し,腫瘍寛解後に辺縁系脳炎を発症した抗Hu抗体陽性傍腫瘍性神経症候群の1例
- 症例報告 感覚性ニューロパチーが先行し,腫瘍寛解後に辺縁系脳炎を発症した抗Hu抗体陽性傍腫瘍性神経症候群の1例
- ショウレイ ホウコク カンカクセイ ニューロパチー ガ センコウ シ,シュヨウカンカイゴ ニ ヘンエンケイ ノウエン オ ハッショウ シタ コウHu コウタイ ヨウセイ ボウ シュヨウセイ シンケイ ショウコウグン ノ 1レイ
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Description
Paraneoplastic limbic encephalitis is a rare neurological disorder that frequently precedes the detection of malignancy. We report the case of a 68-year-old male with small-cell lung cancer who developed paraneoplastic limbic encephalitis associated with presence of the anti-Hu antibody, after achieving complete remission of the tumor by chemotherapy. The patient visited our hospital because of progressive sensory disturbance of the distal extremities at 65 years of age. Though paraneoplastic sensory neuropathy was suspected, we could not find any tumor and he did not improve with steroids or immunoglobulin therapy. Chest computed tomography (CT) revealed large mediastinal lymphadenopathy. He was subsequently diagnosed with small cell lung cancer at one year and three months after the neurological symptoms occurred. As his serum analysis was positive for the anti-Hu antibody, we diagnosed paraneoplastic sensory neuropathy. The lung cancer disappeared with chemotherapy, but he had developed short-term memory loss six months later. Brain fluid attenuated inversion recovery (FLAIR) imaging showed an abnormal high-intensity lesion in the left medial temporal lobe including the hippocampus. We therefore made the diagnosis of paraneoplastic limbic encephalitis following subacute sensory neuropathy associated with the anti-Hu antibody. To our knowledge, this is the first report of a patient presenting with paraneoplastic neurological syndrome in which limbic encephalitis developed after tumor disappearance. So we must recognize the possibility of neurological symptoms occurring during remission. As the mechanism of pathogenesis, delayed neuronal cell damage due to immune responses against the tumor is implicated.
Journal
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- Rinsho Shinkeigaku
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Rinsho Shinkeigaku 53 (4), 287-292, 2013
Societas Neurologica Japonica
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Keywords
Details 詳細情報について
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- CRID
- 1390282680012497408
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- NII Article ID
- 130004921090
- 40019663239
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- NII Book ID
- AN00253207
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- COI
- 1:STN:280:DC%2BC3srntFeqtw%3D%3D
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- ISSN
- 18820654
- 0009918X
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- NDL BIB ID
- 024608511
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- PubMed
- 23603543
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- Text Lang
- ja
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- Data Source
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
- OpenAIRE
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- Abstract License Flag
- Disallowed