Difference between revisions of "Neurodegenerative diseases"

From Libre Pathology
Jump to navigation Jump to search
m (overview)
(→‎Overview: table, disease, clinical)
Line 10: Line 10:
{{familytree  | B01 | | B02 | | B03 | | B04 | |B01=Amyloidoses|B02=Tauopathies|B03=α-synucleinopathies|B04=TDP-43}}
{{familytree  | B01 | | B02 | | B03 | | B04 | |B01=Amyloidoses|B02=Tauopathies|B03=α-synucleinopathies|B04=TDP-43}}
{{familytree/end}}
{{familytree/end}}
===Common diseases===
[[Amyloid]]oses:
*Alzheimer disease (Abeta).
*Creutzfeldt-Jakob disease (PrP).
Taupathies:
*Progressive supranuclear palsy.
*Pick's disease.
Synucleinopathies:
*Parkinson disease.
*Dementia with Lewy bodies.
*Multiple system atrophy.
TDP-43 proteinopathies:
*Amyotrophic alteral sclerosis.
*Frontotemporal lobar degeneration with ubiquitinated inclusions.
====Table===
Disease/pathology/clinical correlation based on ''Dickson'':<ref name=pmid19918325>{{cite journal |author=Dickson DW |title=Neuropathology of non-Alzheimer degenerative disorders |journal=Int J Clin Exp Pathol |volume=3 |issue=1 |pages=1–23 |year=2009 |pmid=19918325 |pmc=2776269 |doi= |url=http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2776269/?tool=pubmed}}</ref>
{| class="wikitable sortable" style="margin-left:auto;margin-right:auto"
| '''Disease'''
| '''Mutated protein'''
| '''Distribution'''
| '''Clinical'''
| '''Image'''
|-
| Alzheimer disease
| Abeta (mutated ''APP'')
| corticolimbic
| dementia
| Image?
|-
| Creutzfeldt-Jakob disease
| PrP<sup>res</sup>
| cortical & basal ganglia
| rapid progression dementia, <br>movement disorder
| Image?
|-
| Progressive supranuclear palsy
| tau 4R
| basal ganglia, brainstem
| parkinsonism
| Image?
|-
| Pick disease
| tau 3R
| corticolimbic
| dementia + focal <br>cortical syndrome
| Image?
|-
| Parkinson disease
| alpha-synuclein
| brainstem
| parkinsonism
| Image?
|-
| Dementia with Lewy bodies
| alpha-synuclein
| corticolimbic, brainstem
| dementia + parkinsonism
| Image?
|-
| Multiple system atrophy
| alpha-synuclein
| basal ganglia, brainstem, cerebellum
| ataxia, parkinsonism
| Image
|-
| Amyotrophic lateral sclerosis
| TDP-43
| motor neurons
| spasticity, weakness
| Image
|-
| Frontotemporal lobar degeneration with ubiquitinated inclusions
| TDP-43
| cortex, basal ganglia
| dementia, focal cortical syndromes
| Image?
|- <!--
| Disease
| Mutated protein
| Distribution
| Clinical
| Image -->
|}
==IHC==
*AT-8 = stains phosphorylated tau.<ref name=pmid19946779>{{cite journal |author=Seelaar H, Klijnsma KY, de Koning I, ''et al.'' |title=Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration |journal=J. Neurol. |volume=257 |issue=5 |pages=747–53 |year=2010 |month=May |pmid=19946779 |pmc=2864899 |doi=10.1007/s00415-009-5404-z |url=http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2864899/}}</ref>
*p62; poli-ubiquitin-binding protein p62.<ref name=pmid19946779/>
*TDP-43.


==General DDx of dementia==
==General DDx of dementia==

Revision as of 16:56, 12 November 2010

Neurodegenerative diseases is a big part of neuropathology.

Overview

They are essentially progressive and selective neuron loss. Clinically, they are not unique. They are defined by molecular pathology.[1]

Molecular schema of neurodegenerative disorders:[1]

 
 
 
 
 
 
Neurodegenerative
disorders
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Amyloidoses
 
Tauopathies
 
α-synucleinopathies
 
TDP-43
 

Common diseases

Amyloidoses:

  • Alzheimer disease (Abeta).
  • Creutzfeldt-Jakob disease (PrP).

Taupathies:

  • Progressive supranuclear palsy.
  • Pick's disease.

Synucleinopathies:

  • Parkinson disease.
  • Dementia with Lewy bodies.
  • Multiple system atrophy.

TDP-43 proteinopathies:

  • Amyotrophic alteral sclerosis.
  • Frontotemporal lobar degeneration with ubiquitinated inclusions.

=Table

Disease/pathology/clinical correlation based on Dickson:[1]

Disease Mutated protein Distribution Clinical Image
Alzheimer disease Abeta (mutated APP) corticolimbic dementia Image?
Creutzfeldt-Jakob disease PrPres cortical & basal ganglia rapid progression dementia,
movement disorder 		Image?
Progressive supranuclear palsy tau 4R basal ganglia, brainstem parkinsonism Image?
Pick disease tau 3R corticolimbic dementia + focal
cortical syndrome 		Image?
Parkinson disease alpha-synuclein brainstem parkinsonism Image?
Dementia with Lewy bodies alpha-synuclein corticolimbic, brainstem dementia + parkinsonism Image?
Multiple system atrophy alpha-synuclein basal ganglia, brainstem, cerebellum ataxia, parkinsonism Image
Amyotrophic lateral sclerosis TDP-43 motor neurons spasticity, weakness Image
Frontotemporal lobar degeneration with ubiquitinated inclusions TDP-43 cortex, basal ganglia dementia, focal cortical syndromes Image?

IHC

  • AT-8 = stains phosphorylated tau.[2]
  • p62; poli-ubiquitin-binding protein p62.[2]
  • TDP-43.

General DDx of dementia

  • Alzheimer's dementia.
  • Vascular.
    • Multi-infarct dementia.
  • Parkinson's associated dementia.
  • Lewy body dementia.
  • Alcohol-related dementia.
  • Fronto-temporal dementia (Pick disease).
  • Multisystem atrophy.

Mnemonic VITAMIN D VEST:[3]

  • Vitamin deficiency (B12, folate, thiamine).
  • Infection (HIV).
  • Trauma.
  • Anoxia.
  • Metabolic (Diabetes).
  • Intracranial tumour.
  • Normal pressure hydrocephalus.
  • Degenerative (Alzheimer's, Huntington's, CJD).
  • Vascular.
  • Endocrine.
  • Space occupying lesion (chronic subdural hematoma).
  • Toxins (alcohol).

Lewy body dementia

  • Parkinsonian features.
  • Hallucinations (visual).
  • Progressive cog. decline with fluctuations.

Multiple system atrophy

  • Alpha-synuclein-rich glial cytoplasmic inclusions - finding at autopsy.[4]
    • Alpha-synuclein is implicated in a number of neurodegenerative diseases.[5]

Progressive supranuclear palsy

General

  • AKA Steele-Richardson-Olszewski syndrome.
  • Diagnosis: clinical.[6]

Microscopic

Features:

  • Neurofibrillary tangles.[6][7]

Huntington disease

General

  • Autosomal dominant inheritance.
  • Mutation: unstable CAG repeat.[8]

Gross

  • Missing caudate.[9]

Image: Huntington's disease (ouhsc.edu).

See also

References

  1. ↑ 1.0 1.1 1.2 Dickson DW (2009). "Neuropathology of non-Alzheimer degenerative disorders". Int J Clin Exp Pathol 3 (1): 1–23. PMC 2776269. PMID 19918325. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2776269/?tool=pubmed.
  2. ↑ 2.0 2.1 Seelaar H, Klijnsma KY, de Koning I, et al. (May 2010). "Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration". J. Neurol. 257 (5): 747–53. doi:10.1007/s00415-009-5404-z. PMC 2864899. PMID 19946779. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2864899/.
  3. ↑ TN06 PS19
  4. ↑ Wenning, GK.; Stefanova, N.; Jellinger, KA.; Poewe, W.; Schlossmacher, MG. (Sep 2008). "Multiple system atrophy: a primary oligodendrogliopathy.". Ann Neurol 64 (3): 239-46. doi:10.1002/ana.21465. PMID 18825660.
  5. ↑ Uversky, VN. (Oct 2008). "Alpha-synuclein misfolding and neurodegenerative diseases.". Curr Protein Pept Sci 9 (5): 507-40. PMID 18855701.
  6. ↑ 6.0 6.1 URL: http://emedicine.medscape.com/article/1151430-overview. Accessed on: 11 November 2010.
  7. ↑ Williams DR, Lees AJ (March 2009). "Progressive supranuclear palsy: clinicopathological concepts and diagnostic challenges". Lancet Neurol 8 (3): 270–9. doi:10.1016/S1474-4422(09)70042-0. PMID 19233037.
  8. ↑ Kumar P, Kalonia H, Kumar A (2010). "Huntington's disease: pathogenesis to animal models". Pharmacol Rep 62 (1): 1–14. PMID 20360611.
  9. ↑ URL: http://moon.ouhsc.edu/kfung/jty1/NeuroTest/Q07-Ans.htm. Accessed on: 29 October 2010.
Retrieved from "https://librepathology.org/w/index.php?title=Neurodegenerative_diseases&oldid=2706"