2019
DOI: 10.5334/tohm.480
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Subacute Sclerosing Panencephalitis Causing Rapidly Progressive Dementia and Myoclonic Jerks in a Sexagenarian Woman

Abstract: Background: Subacute sclerosing panencephalitis (SSPE) is a disease of childhood and adolescence, but can affect adults. Rapidly progressive cognitive decline, seizures including myoclonic jerks, spasticity, ataxia, visual disturbances, and incontinence are typical manifestations. Case report: A 62-year-old woman who presented with rapidly progressive dementia and myoclonus was diagnosed with SSPE. There was resolution of the movement disorder with clonazepam and valproic acid treatment and some amelioration o… Show more

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Cited by 4 publications
(4 citation statements)
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“…By no means is this list completely inclusive, but it speaks to a vast realm of possibilities that should be considered in addition to subacute sclerosing panencephalitis. 18,20,[25][26][27]…”
Section: Differential Diagnosismentioning
confidence: 99%
“…By no means is this list completely inclusive, but it speaks to a vast realm of possibilities that should be considered in addition to subacute sclerosing panencephalitis. 18,20,[25][26][27]…”
Section: Differential Diagnosismentioning
confidence: 99%
“…Mostly affecting children, the virus causes neurodegeneration, inflammation, and demyelination of the central nervous system resulting in death before the age of three. Although rare, it has been noticed in older adults where SSPE remerges from a dormant state and causes dementia [162].…”
Section: Subacute Sclerosing Panencephalitismentioning
confidence: 99%
“…Reyes and colleagues reported a 62-year-old woman who presented with rapidly progressive dementia and myoclonus and was later diagnosed as having SSPE. 4 This is one of the three oldest recorded patients with SSPE. There are two additional earlier reports of SSPE where patients presented after the age of 60 years.…”
mentioning
confidence: 96%
“…MRI consistently demonstrated T2 hyperintensities in the periventricular region, predominantly affecting the occipitoparietal lobes (Table 1). 414 Creutzfeldt–Jakob disease and anti- N -methyl- d -aspartate-receptor encephalitis are often close differential diagnoses. The demonstration of elevated CSF antimeasles antibody titer and brain biopsy helps in establishing the diagnosis of SSPE.…”
mentioning
confidence: 99%