Evidence map›Paper›PMID 40079251›Full record

ArticleNeuropathology : official journal of the Japanese Society of Neuropathology2025

Unprecedented Combination of Rare Degenerative Pathologies in an Octogenarian Ex-Football Player.

Shelley L Forrest, Nusrat Sadia, Mozhgan Khodadadi, Charles Tator, Robin Green, Maria Carmela Tartaglia, Gabor G Kovacs

Abstract readCase Reports
In one paragraph

Article in Neuropathology : official journal of the Japanese Society of Neuropathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Unprecedented Combination of Rare Degenerative Pathologies in an Octogenarian Ex-Football Player.Neuropathology : official journal of the Japanese Society of Neuropathology · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Shelley L ForrestTanz Centre for Research in Neurodegenerative Disease, University of Toronto, Toronto, Canada.
Nusrat SadiaCanadian Concussion Centre, Krembil Brain Institute, University Health Network, University of Toronto, Toronto, Canada.
Mozhgan KhodadadiCanadian Concussion Centre, Krembil Brain Institute, University Health Network, University of Toronto, Toronto, Canada.
Charles TatorCanadian Concussion Centre, Krembil Brain Institute, University Health Network, University of Toronto, Toronto, Canada.
Robin GreenCanadian Concussion Centre, Krembil Brain Institute, University Health Network, University of Toronto, Toronto, Canada.
Maria Carmela TartagliaCanadian Concussion Centre, Krembil Brain Institute, University Health Network, University of Toronto, Toronto, Canada.
Gabor G KovacsTanz Centre for Research in Neurodegenerative Disease, University of Toronto, Toronto, Canada.ORCID https://orcid.org/0000-0003-3841-5511

Funding

ROSSY FAMILY FOUNDATION
6 · The paper itself

Abstract

A 79-year-old former professional football player presented with language deficits and cognitive changes. A year later, he had difficulty completing sentences, and 3 years after onset, was reduced to one-word answers. He developed severe apathy and agitation, and became more impulsive. He eventually became mute and had difficulty with walking and balance. The patient had mild repetitive head injury while playing football and three concussions. Magnetic resonance imaging revealed left > right frontotemporal atrophy. Duration of illness was 6 years. Neuropathology revealed an unexpected number and diversity of degenerative pathologies, including chronic traumatic encephalopathy (CTE, high level), high level Alzheimer's disease neuropathologic change (A3B3C3), limbic Lewy body disease, cerebral amyloid angiopathy (type 2), argyrophilic grain disease (Stage 2), and neuronal intranuclear hyaline inclusion body disease. In addition, there was selective and asymmetric involvement of the corticospinal tract with globular oligodendroglial tau pathology corresponding to globular glial tauopathy (Type II). The patchy and irregular accentuation of cortical tau pathology, particularly in the depths of sulci and accumulation around blood vessels, allows the diagnosis of CTE-neuropathologic change. This diagnosis correlated with the past medical history of multiple concussions. In addition, the patient had an unprecedented number and combination of additional degenerative pathologies, including those that are rare, and how they contributed to the clinical symptoms is difficult to interpret. Globular glial tauopathy Type II is a rare disorder that has been mostly reported in association with progressive supranuclear gaze palsy, and these observations support the notion that globular glial tauopathy Type II is an independent entity with isolated corticospinal tract involvement. These observations highlight that rare disorders can occur in the same individual and be overlooked, especially when there is more obvious pathology. It is essential for neuropathologists to consider an extensive array of neuropathological examinations when assessing patients with neurodegenerative disorders.

Indexed as

BrainChronic Traumatic EncephalopathyFootballNeurodegenerative DiseasesAgedBrain ConcussionHumansMalechronic traumatic encephalopathyconcussionglobular glial tauopathymixed pathology

Identifiers

PMID40079251
PMCPMC12309147

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.