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Published in: Journal of Neurology 4/2014

01-04-2014 | Original Communication

A follow-up 18F-FDG brain PET study in a case of Hashimoto's encephalopathy causing drug-resistant status epilepticus treated with plasmapheresis

Authors: Elisa Pari, Fabrizio Rinaldi, Enrico Premi, Maria Codella, Renata Rao, Barbara Paghera, Maria Beatrice Panarotto, Giovanni De Maria, Alessandro Padovani

Published in: Journal of Neurology | Issue 4/2014

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Abstract

Hashimoto's encephalopathy (HE) is a rare neuropsychiatric syndrome associated with antithyroid antibodies. It may have an acute onset (episodes of cerebral ischemia, seizure, and psychosis) or it may present as an indolent form (depression, cognitive decline, myoclonus, tremors, and fluctuations in level of consciousness). We here describe a case of encephalopathy presenting as non-convulsive status epilepticus associated with Hashimoto's thyroiditis (HT), unresponsive to corticosteroid therapy, with improvement after plasma exchange treatment. A previously healthy 19-year-old woman, presented generalized tonic–clonic seizures. About a month later, she manifested a speech disorder characterized by difficulties in the production and comprehension of language. Within a few days she also developed confusion and difficulties in recognizing familiar places, with gradual worsening over time. EEG revealed a non-convulsive status epilepticus (NCSE). CSF examination showed slightly elevated cell count and four oligoclonal bands. MRI was unremarkable, and 18F-FDG brain PET showed widespread hypometabolism, mostly in posterior regions bilaterally. Laboratory and ultrasound findings showed signs of HT. Treatment with steroid was introduced without any improvement. After five sessions of plasma exchange there was a decrease of antithyroid antibodies, as well as EEG and clinical improvement. Three months after discharge 18F-FDG brain PET showed a complete normalization of the picture, and the patient was asymptomatic. This report emphasizes the successful treatment of HE with plasma exchange in a patient who presented with NCSE. Based on the actual evidence, the term “Encephalopathy associated with Hashimoto’s thyroiditis” may be the most proper. Furthermore, to our knowledge, this is the first case of an adult patient studied twice with an 18F-FDG brain PET: prior to treatment with plasma exchange, and at 3 months follow-up when the patient was clinically completely asymptomatic. Studies in more patients are needed to clarify the relevance of 18F-FDG brain PET as a possible diagnostic tool for HE.
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Metadata
Title
A follow-up 18F-FDG brain PET study in a case of Hashimoto's encephalopathy causing drug-resistant status epilepticus treated with plasmapheresis
Authors
Elisa Pari
Fabrizio Rinaldi
Enrico Premi
Maria Codella
Renata Rao
Barbara Paghera
Maria Beatrice Panarotto
Giovanni De Maria
Alessandro Padovani
Publication date
01-04-2014
Publisher
Springer Berlin Heidelberg
Published in
Journal of Neurology / Issue 4/2014
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-013-7228-0

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