open access

Vol 51, No 2 (2017)
Case reports
Submitted: 2016-09-23
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The Heidenhain variant of Creutzfeldt–Jakob disease and concomitant tau pathology: A case report

Edvard Ehler1, Michael Pipka1, Alena Meleková1, Petra Mandysová21, Silvie Johanidesová3, Radoslav Matěj45, Robert Rusina36
DOI: 10.1016/j.pjnns.2017.01.011
·
Neurol Neurochir Pol 2017;51(2):197-200.
Affiliations
  1. Department of Neurology, Regional Hospital Pardubice, Czech Republic
  2. Faculty of Health Studies, University of Pardubice, Pardubice, Czech Republic
  3. Department of Neurology and Centre of Clinical Neuroscience, First Faculty of Medicine, Charles University in Prague and the General University Hospital, Prague, Czech Republic
  4. Department of Pathology and Molecular Medicine, Thomayer Hospital, Prague, Czech Republic
  5. Department of Pathology, First Faculty of Medicine, Charles University in Prague and the General University Hospital, Prague, Czech Republic
  6. Department of Neurology, Thomayer Hospital, Prague, Czech Republic

open access

Vol 51, No 2 (2017)
Case reports
Submitted: 2016-09-23

Abstract

•The Heidenhain form of CJD is a rare variant with predominantly visual symptoms.•Clinical findings correlate with involvement of posterior cortical regions.•MRI found typical cortical hyperintensities in the occipital regions.•Neuropathology revealed histopathological changes consistent with prion disease.•Hyperphosphorylated tau deposits were an additional and interesting finding in our case.

Abstract

•The Heidenhain form of CJD is a rare variant with predominantly visual symptoms.•Clinical findings correlate with involvement of posterior cortical regions.•MRI found typical cortical hyperintensities in the occipital regions.•Neuropathology revealed histopathological changes consistent with prion disease.•Hyperphosphorylated tau deposits were an additional and interesting finding in our case.

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Keywords

Prion, Creutzfeldt–Jakob disease, Visuospatial dysfunction, Heidenhain variant

About this article
Title

The Heidenhain variant of Creutzfeldt–Jakob disease and concomitant tau pathology: A case report

Journal

Neurologia i Neurochirurgia Polska

Issue

Vol 51, No 2 (2017)

Pages

197-200

Page views

268

Article views/downloads

541

DOI

10.1016/j.pjnns.2017.01.011

Bibliographic record

Neurol Neurochir Pol 2017;51(2):197-200.

Keywords

Prion
Creutzfeldt–Jakob disease
Visuospatial dysfunction
Heidenhain variant

Authors

Edvard Ehler
Michael Pipka
Alena Meleková
Petra Mandysová
Silvie Johanidesová
Radoslav Matěj
Robert Rusina

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