Literature DB >> 19822786

Polymyoclonus, laryngospasm, and cerebellar ataxia associated with adenocarcinoma and multiple neural cation channel autoantibodies.

Shen-Yang Lim1, Warren P Mason, Nathan P Young, Robert Chen, James H Bower, Andrew McKeon, Sean J Pittock, Anthony E Lang.   

Abstract

OBJECTIVE: To describe and provide audiovisual documentation of a syndrome of polymyoclonus, laryngospasm, and cerebellar ataxia associated with adenocarcinoma and multiple neural cation channel autoantibodies.
DESIGN: Case report with video.
SETTING: University hospitals. Patient A 69-year-old woman presented with subacute onset of whole-body tremulousness and laryngospasm attributed to gastroesophageal reflux.
RESULTS: Further evaluation revealed polymyoclonus, cerebellar ataxia, and laryngospasm suspicious of an underlying malignant neoplasm. Surface electromyography of multiple limb muscles confirmed the presence of polymyoclonus. The patient was seropositive for P/Q-type voltage-gated calcium channel antibody; subsequently, whole-body fluorine 18 fluorodeoxyglucose positron emission tomography and cervical lymph node biopsy revealed widespread metastatic adenocarcinoma. Follow-up serologic evaluation revealed calcium channel antibodies (P/Q type and N type) and potassium channel antibody.
CONCLUSIONS: We highlight the importance of recognizing polymyoclonus. To our knowledge, this is also the first description of a syndrome of polymyoclonus, laryngospasm, and ataxia associated with adenocarcinoma and these cation channel antibodies.

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Year:  2009        PMID: 19822786     DOI: 10.1001/archneurol.2009.203

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  1 in total

1.  A Case of Paraneoplastic Myoclonus Attributed to Non-Small Cell Lung Cancer.

Authors:  Jennifer L Nichols; Brett J Lee; Kathryn A Chung
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2020-06-16
  1 in total

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