• This record comes from PubMed

Corpus callosum hypersignals and focal atrophy: Neuroimaging findings in globular glial tauopathy type I

. 2022 Jan ; 29 (1) : 324-328. [epub] 20210912

Language English Country Great Britain, England Media print-electronic

Document type Journal Article, Research Support, Non-U.S. Gov't

BACKGROUND AND PURPOSE: Globular glial tauopathies (GGTs) have heterogeneous presentations; little evidence regarding typical clinical and magnetic resonance imaging (MRI) presentations are available. METHODS: We retrospectively assessed MRIs from three postmortem-confirmed GGT cases, in two patients with atypical progressive aphasia and one with corticobasal syndrome. RESULTS: We suggest that four principal concomitant MRI findings characterize GGT type I: a sagittal callosal hyperintense band, marked focal callosal atrophy suggesting white matter degeneration originating in cortical areas responsible for symptoms (anterior atrophy in predominantly language manifestations and posterior atrophy in predominantly apraxia), periventricular white matter lesions, and mild-to-moderate brain stem atrophy. CONCLUSIONS: We observed four concomitant MRI abnormalities in patients with atypical dementia, parkinsonism, and late incomplete supranuclear gaze palsy. Two patients had atypical progressive aphasia and one had corticobasal syndrome.

See more in PubMed

Ahmed Z, Bigio EH, Budka H, et al. Globular glial tauopathies (GGT): consensus recommendations. Acta Neuropathol. 2013;126:537‐544. PubMed PMC

Rusina R, Csefalvay Z, Kovacs GG, et al. Globular glial tauopathy type I presenting as atypical progressive aphasia, with comorbid limbic‐predominant age‐related TDP‐43 encephalopathy. Front Aging Neurosci. 2019;11:336. PubMed PMC

Witelson SF. Hand and sex differences in the isthmus and genu of the human corpus callosum. A postmortem morphological study. Brain. 1989;112:799‐835. PubMed

Hofer S, Frahm J. Topography of the human corpus callosum revisited–comprehensive fiber tractography using diffusion tensor magnetic resonance imaging. NeuroImage. 2006;32:989‐994. PubMed

Williams DR, Holton JL, Strand C, et al. Pathological tau burden and distribution distinguishes progressive supranuclear palsy‐parkinsonism from Richardson's syndrome. Brain. 2007;130:1566‐1576. PubMed

Kovacs GG, Lukic MJ, Irwin DJ, et al. Distribution patterns of tau pathology in progressive supranuclear palsy. Acta Neuropathol. 2020;140:99‐119. PubMed PMC

Ohno Y, Ikeda T, Sakurai K, et al. Rapid progression of white matter signal changes and frontotemporal atrophy in globular glial tauopathy. J Neuropathol Exp Neurol. 2021;80:480‐483. PubMed

Hirano M, Iritani S, Fujishiro H, et al. Globular glial tauopathy Type I presenting with behavioral variant frontotemporal dementia. Neuropathology. 2020;40:515‐525. PubMed

Tanaka H, Kawakatsu S, Toyoshima Y, et al. Globular glial tauopathy Type II: Clinicopathological study of two autopsy cases. Neuropathology. 2019;39:111‐119. PubMed

Josephs KA, Katsuse O, Beccano‐Kelly DA, et al. Atypical progressive supranuclear palsy with corticospinal tract degeneration. J Neuropathol Exp Neurol. 2006;65:396‐405. PubMed

Liu AJ, Chang JE, Naasan G, et al. Progressive supranuclear palsy and primary lateral sclerosis secondary to globular glial tauopathy: a case report and a practical theoretical framework for the clinical prediction of this rare pathological entity. Neurocase. 2020;26:91‐97. PubMed PMC

Yamauchi H, Fukuyama H, Nagahama Y, et al. Comparison of the pattern of atrophy of the corpus callosum in frontotemporal dementia, progressive supranuclear palsy, and Alzheimer's disease. J Neurol Neurosurg Psychiatry. 2000;69:623‐629. PubMed PMC

Frederiksen KS. Corpus callosum in aging and dementia. Dan Med J. 2013;60:B4721. PubMed

Forrest SL, Kril JJ, Kovacs GG. Association between globular glial tauopathies and frontotemporal dementia‐expanding the spectrum of gliocentric disorders: a review. JAMA Neurol. 2021;78:1004‐1014. PubMed

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...