Literature DB >> 17923638

Potassium channel antibody associated encephalopathy presenting with a frontotemporal dementia like syndrome.

Andrew McKeon1, Michael Marnane, Martin O'connell, John P Stack, Peter J Kelly, Timothy Lynch.   

Abstract

OBJECTIVE: To describe a patient who presented with features suggestive of frontotemporal dementia (FTD) but with some atypical findings and antibodies to neuronal voltage-gated potassium channels (VGKC-Abs).
DESIGN: Case report.
SETTING: Mater Misericordiae University Hospital, Dublin, Ireland.
RESULTS: An 82-year-old man presented with progressive changes in personality, social conduct, and executive function with preservation of memory, deteriorating from baseline to requiring acute hospitalization within 6 months. Transient deterioration (episodic speech arrest) with spontaneous recovery, atypical for frontotemporal dementia, was observed. The patient had an elevated VGKC-Ab titer (2624 pM [normal range, < 100 pM]), elevated protein levels in cerebrospinal fluid, and a negative evaluation for malignancy. Magnetic resonance imaging of brain was normal but [(18)F]-fluorodeoxyglucose positron emission tomographic imaging revealed bifrontal hypometabolism. A marked and sustained improvement with steroid therapy was observed.
CONCLUSION: Workup for a potentially reversible autoimmune-mediated encephalopathy, including a VGKC-Ab titer, should be considered in patients presenting with rapidly progressive behavioral and cognitive decline.

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Year:  2007        PMID: 17923638     DOI: 10.1001/archneur.64.10.1528

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


  24 in total

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