Literature DB >> 10840273

Traumatic axonal injury: practical issues for diagnosis in medicolegal cases.

J F Geddes1, H L Whitwell, D I Graham.   

Abstract

In the 25 years or so after the first clinicopathological descriptions of diffuse axonal injury (DAI), the criterion for diagnosing recent traumatic white matter damage was the identification of swollen axons ('bulbs') on routine or silver stains, in the appropriate clinical setting. In the last decade, however, experimental work has given us greater understanding of the cellular events initiated by trauma to axons, and this in turn has led to the adoption of immunocytochemical methods to detect markers of axonal damage in both routine and experimental work. These methods have shown that traumatic axonal injury (TAI) is much more common than previously realized, and that what was originally described as DAI occupies only the most severe end of a spectrum of diffuse trauma-induced brain injury. They have also revealed a whole field of previously unrecognized white matter pathology, in which axons are diffusely damaged by processes other than head injury; this in turn has led to some terminological confusion in the literature. Neuropathologists are often asked to assess head injuries in a forensic setting: the diagnostic challenge is to sort out whether the axonal damage detected in a brain is indeed traumatic, and if so, to decide what - if anything - can be inferred from it. The lack of correlation between well-documented histories and neuropathological findings means that in the interpretation of assault cases at least, a diagnosis of 'TAI' or 'DAI' is likely to be of limited use for medicolegal purposes.

Entities:  

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Year:  2000        PMID: 10840273     DOI: 10.1046/j.1365-2990.2000.026002105.x

Source DB:  PubMed          Journal:  Neuropathol Appl Neurobiol        ISSN: 0305-1846            Impact factor:   8.090


  34 in total

1.  Partial interruption of axonal transport due to microtubule breakage accounts for the formation of periodic varicosities after traumatic axonal injury.

Authors:  Min D Tang-Schomer; Victoria E Johnson; Peter W Baas; William Stewart; Douglas H Smith
Journal:  Exp Neurol       Date:  2011-11-04       Impact factor: 5.330

2.  Controlled cortical impact traumatic brain injury in 3xTg-AD mice causes acute intra-axonal amyloid-β accumulation and independently accelerates the development of tau abnormalities.

Authors:  Hien T Tran; Frank M LaFerla; David M Holtzman; David L Brody
Journal:  J Neurosci       Date:  2011-06-29       Impact factor: 6.167

3.  Controversies in pediatric forensic pathology.

Authors:  Henry F Krous; Roger W Byard
Journal:  Forensic Sci Med Pathol       Date:  2005-03       Impact factor: 2.007

4.  Inhibition of JNK by a peptide inhibitor reduces traumatic brain injury-induced tauopathy in transgenic mice.

Authors:  Hien T Tran; Laura Sanchez; David L Brody
Journal:  J Neuropathol Exp Neurol       Date:  2012-02       Impact factor: 3.685

5.  Diffusion tensor imaging detects axonal injury in a mouse model of repetitive closed-skull traumatic brain injury.

Authors:  Rachel E Bennett; Christine L Mac Donald; David L Brody
Journal:  Neurosci Lett       Date:  2012-02-17       Impact factor: 3.046

Review 6.  Traumatic brain injury and amyloid-β pathology: a link to Alzheimer's disease?

Authors:  Victoria E Johnson; William Stewart; Douglas H Smith
Journal:  Nat Rev Neurosci       Date:  2010-05       Impact factor: 34.870

7.  Mechanical disruption of the blood-brain barrier following experimental concussion.

Authors:  Victoria E Johnson; Maura T Weber; Rui Xiao; D Kacy Cullen; David F Meaney; William Stewart; Douglas H Smith
Journal:  Acta Neuropathol       Date:  2018-02-19       Impact factor: 17.088

8.  Multi-Site Optical Monitoring of Spinal Cord Ischemia during Spine Distraction.

Authors:  David R Busch; Wei Lin; Chunyu Cai; Alissa Cutrone; Jakub Tatka; Brandon J Kovarovic; Arjun G Yodh; Thomas F Floyd; James Barsi
Journal:  J Neurotrauma       Date:  2020-07-20       Impact factor: 5.269

9.  CLARITY reveals a more protracted temporal course of axon swelling and disconnection than previously described following traumatic brain injury.

Authors:  Maura T Weber; John D Arena; Rui Xiao; John A Wolf; Victoria E Johnson
Journal:  Brain Pathol       Date:  2018-12-27       Impact factor: 6.508

10.  Multiple proteins implicated in neurodegenerative diseases accumulate in axons after brain trauma in humans.

Authors:  Kunihiro Uryu; Xiao-Han Chen; Dan Martinez; Kevin D Browne; Victoria E Johnson; David I Graham; Virginia M-Y Lee; John Q Trojanowski; Douglas H Smith
Journal:  Exp Neurol       Date:  2007-07-10       Impact factor: 5.330

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