Postencephalitic Parkinsonism: Unique Pathological and Clinical Features—Preliminary Data

Postencephalitic parkinsonism (PEP) is suggested to show a virus-induced pathology, which is different from classical idiopathic Parkinson’s disease (PD) as there is no α-synuclein/Lewy body pathology. However, PEP shows a typical clinical representation of motor disturbances. In addition, compared...

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Published inCells (Basel, Switzerland) Vol. 13; no. 18; p. 1511
Main Authors Strobel, Sabrina, Sian-Hulsmann, Jeswinder, Tappe, Dennis, Jellinger, Kurt, Riederer, Peter, Monoranu, Camelia-Maria
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 01.09.2024
MDPI
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ISSN2073-4409
2073-4409
DOI10.3390/cells13181511

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Summary:Postencephalitic parkinsonism (PEP) is suggested to show a virus-induced pathology, which is different from classical idiopathic Parkinson’s disease (PD) as there is no α-synuclein/Lewy body pathology. However, PEP shows a typical clinical representation of motor disturbances. In addition, compared to PD, there is no iron-induced pathology. The aim of this preliminary study was to compare PEP with PD regarding iron-induced pathology, using histochemistry methods on paraffin-embedded post-mortem brain tissue. In the PEP group, iron was not seen, except for one case with sparse perivascular depositions. Rather, PEP offers a pathology related to tau-protein/neurofibrillary tangles, with mild to moderate memory deficits only. It is assumed that this virus-induced pathology is due to immunological dysfunctions causing (neuro)inflammation-induced neuronal network disturbances as events that trigger clinical parkinsonism. The absence of iron deposits implies that PEP cannot be treated with iron chelators. The therapy with L-Dopa is also not an option, as L-Dopa only leads to an initial slight improvement in symptoms in isolated cases.
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These authors contributed equally to this work.
These authors also contributed equally to this work.
ISSN:2073-4409
2073-4409
DOI:10.3390/cells13181511