Difference between revisions of "Neurodegenerative diseases"
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| '''Distribution''' | | '''Distribution''' | ||
| '''Clinical''' | | '''Clinical''' | ||
| '''Histology''' | |||
| '''Image''' | | '''Image''' | ||
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| corticolimbic, usu. <br>spares occipital | | corticolimbic, usu. <br>spares occipital | ||
| dementia | | dementia | ||
| histology? | |||
| Image? | | Image? | ||
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| cortical & basal ganglia | | cortical & basal ganglia | ||
| dementia (rapid progression), <br>movement disorder | | dementia (rapid progression), <br>movement disorder | ||
| plaques, neurofibrillary tangles ??? | |||
| Image? | | Image? | ||
|- | |- | ||
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| basal ganglia, brainstem | | basal ganglia, brainstem | ||
| parkinsonism | | parkinsonism | ||
| histology? | |||
| Image? | | Image? | ||
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| corticolimbic | | corticolimbic | ||
| dementia + focal <br>cortical syndrome | | dementia + focal <br>cortical syndrome | ||
| Pick body ??? | |||
| Image? | | Image? | ||
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| brainstem | | brainstem | ||
| parkinsonism | | parkinsonism | ||
| histology? | |||
| Image? | | Image? | ||
|- | |- | ||
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| corticolimbic, brainstem | | corticolimbic, brainstem | ||
| dementia + parkinsonism | | dementia + parkinsonism | ||
| histology? | |||
| Image? | | Image? | ||
|- | |- | ||
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| basal ganglia, brainstem, cerebellum | | basal ganglia, brainstem, cerebellum | ||
| parkinsonism, ataxia | | parkinsonism, ataxia | ||
| histology? | |||
| Image | | Image | ||
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| motor neurons | | motor neurons | ||
| spasticity, weakness | | spasticity, weakness | ||
| histology? | |||
| Image | | Image | ||
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| cortex, basal ganglia | | cortex, basal ganglia | ||
| dementia, focal cortical syndromes | | dementia, focal cortical syndromes | ||
| histology? | |||
| Image? | | Image? | ||
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| Distribution | | Distribution | ||
| Clinical | | Clinical | ||
| histology? | |||
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*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> | *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/> | *p62; poli-ubiquitin-binding protein p62.<ref name=pmid19946779/> | ||
*TDP-43. | *TDP-43 - normally in the nucleus. | ||
**Pathologic:<ref>URL: [http://archneur.ama-assn.org/cgi/content/full/65/5/636/NOC70108F2 http://archneur.ama-assn.org/cgi/content/full/65/5/636/NOC70108F2]. Accessed on: 20 November 2010.</ref> | |||
***''Fibrillar'' or ''skein-like formations'' = cytoplasmic staining. | |||
***''Neurites'' = squiggly appearance. | |||
==Clinical perspective (becoming obsolete)== | ==Clinical perspective (becoming obsolete)== | ||
Revision as of 19:30, 20 November 2010
Neurodegenerative diseases is a big part of neuropathology.
Overview
- They are essentially progressive and selective neuron loss.
- Clinically, they are not unique, e.g. dementia can be caused by several diseases (with different molecular etiologies).
- They are defined by molecular pathology.[1]
- The diseases are due to the accumulation of abnormal protein.
- The amino acid sequence of the protein may be completely normal. The problem may just be folding/protein conformation.
- The diseases are due to the accumulation of abnormal protein.
Molecular schema of neurodegenerative disorders:[1]
| Neurodegenerative disorders | |||||||||||||||||||||||||||||||||
| Amyloidoses | Tauopathies | α-synucleinopathies | TDP-43 | ||||||||||||||||||||||||||||||
Common diseases
- Alzheimer disease (Abeta).
- Creutzfeldt-Jakob disease (PrP).
Taupathies:
- Progressive supranuclear palsy.
- Pick's disease.
Synucleinopathies:[2]
- 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 | Histology | Image |
| Alzheimer disease | Abeta (mutated APP) | corticolimbic, usu. spares occipital |
dementia | histology? | Image? |
| Creutzfeldt-Jakob disease | PrPres (mutated PrP) | cortical & basal ganglia | dementia (rapid progression), movement disorder |
plaques, neurofibrillary tangles ??? | Image? |
| Progressive supranuclear palsy | tau 4R | basal ganglia, brainstem | parkinsonism | histology? | Image? |
| Pick disease | tau 3R | corticolimbic | dementia + focal cortical syndrome |
Pick body ??? | Image? |
| Parkinson disease | alpha-synuclein | brainstem | parkinsonism | histology? | Image? |
| Dementia with Lewy bodies |
alpha-synuclein | corticolimbic, brainstem | dementia + parkinsonism | histology? | Image? |
| Multiple system atrophy | alpha-synuclein | basal ganglia, brainstem, cerebellum | parkinsonism, ataxia | histology? | Image |
| Amyotrophic lateral sclerosis (ALS) |
TDP-43 | motor neurons | spasticity, weakness | histology? | Image |
| Frontotemporal lobar degeneration with ubiquitinated inclusions |
TDP-43 | cortex, basal ganglia | dementia, focal cortical syndromes | histology? | Image? |
IHC
- AT-8 = stains phosphorylated tau.[3]
- p62; poli-ubiquitin-binding protein p62.[3]
- TDP-43 - normally in the nucleus.
- Pathologic:[4]
- Fibrillar or skein-like formations = cytoplasmic staining.
- Neurites = squiggly appearance.
- Pathologic:[4]
Clinical perspective (becoming obsolete)
General (mostly useless) DDx
- Alzheimer's dementia - most common.
- Vascular.
- Multi-infarct dementia.
- Parkinson's associated dementia.
- Lewy body dementia.
- Alcohol-related dementia.
- Fronto-temporal dementia (Pick disease).
- Multisystem atrophy.
Mnemonic
Mnemonic VITAMIN D VEST:[5]
- 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).
Functional anatomy of dementia
- Hippocampus (essential for forming new memories).
- Frontal lobe (essential for retrieval of memories).
Lewy body diseases
DDx:
- Parkinson's disease.
- Dementia with Lewy bodies.
Etiology:
- Alpha-synuclein.
Clinical features of Dementia with Lewy bodies:
- Parkinsonian features.
- Hallucinations (visual).
- Progressive cognitive decline with fluctuations.
Multiple system atrophy
Clinical findings variable:
- Parkinsonism (stiatonigral degeneration).
- Ataxia (olivo-panto-cerebellar degeneration).
Etiology:
- Alpha-synuclein-rich glial cytoplasmic inclusions - finding at autopsy.[6]
- Inclusions in oligodendrocytes.[7]
Progressive supranuclear palsy
General
Microscopic
- Globose neurofibrillary tangles in neurons.
- Coiled bodies in oligodendrocytes.
Huntington disease
General
- Autosomal dominant inheritance.
- Mutation: unstable CAG repeat.[10]
Gross
- Missing caudate.[11]
Image: Huntington's disease (ouhsc.edu).
Binswanger's disease
General
- Multi-infarct dementia affecting subcortical white matter.
- Waste-basket diagnosis; diagnosed if CADASIL and amyloidosis have been excluded.
- Diagnosis has been controversial -- most with this entity (in the past) were diagnosed with Alzheimer's disease.
Microscopic
Features:
- Subcortical lesions that replace the myelin consisting of macrophages.
Prion diseases
Etiology:[12]
- Misfolded cell-surface protein called PrP(C).
Includes:[12]
- Creutzfeldt-Jakob disease (CJD).
- Sporadic fatal insomnia (sFI).
Creutzfeldt-Jakob disease
General
- Commonly abbreviated as CJD.
- Rare.
- Incurable disease.
- Usually diagnosed clinically.
- Characteristic findings:
- Very rapid decline (3-4 months).
- Characteristic (cortex findings on) neuroradiology.
- Characteristic findings:
Variant Creutzfeldt-Jakob disease (vCJD)
- Associated with bovine spongiform encephalopathy.
- Should sample: spleen, lymph nodes, tonsils.[13]
Microscopic
Features:
- Spongy appearance (cytoplasmic vacuolization[14]).
Images:
See also
References
- ↑ 1.0 1.1 1.2 1.3 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.
- ↑ Uversky, VN. (Oct 2008). "Alpha-synuclein misfolding and neurodegenerative diseases.". Curr Protein Pept Sci 9 (5): 507-40. PMID 18855701.
- ↑ 3.0 3.1 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/.
- ↑ URL: http://archneur.ama-assn.org/cgi/content/full/65/5/636/NOC70108F2. Accessed on: 20 November 2010.
- ↑ TN06 PS19
- ↑ 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.
- ↑ MUN. 16 November 2010.
- ↑ 8.0 8.1 URL: http://emedicine.medscape.com/article/1151430-overview. Accessed on: 11 November 2010.
- ↑ 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.
- ↑ Kumar P, Kalonia H, Kumar A (2010). "Huntington's disease: pathogenesis to animal models". Pharmacol Rep 62 (1): 1–14. PMID 20360611.
- ↑ URL: http://moon.ouhsc.edu/kfung/jty1/NeuroTest/Q07-Ans.htm. Accessed on: 29 October 2010.
- ↑ 12.0 12.1 Watts JC, Balachandran A, Westaway D (March 2006). "The expanding universe of prion diseases". PLoS Pathog. 2 (3): e26. doi:10.1371/journal.ppat.0020026. PMC 1434791. PMID 16609731. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1434791/.
- ↑ Burton, Julian L.; Rutty, Guy N. (2010). The Hospital Autopsy A Manual of Fundamental Autopsy Practice (3rd ed.). Oxford University Press. pp. 83. ISBN 978-0340965146.
- ↑ URL: http://moon.ouhsc.edu/kfung/jty1/opaq/PathQuiz/N0I002-PQ01-M.htm. Accessed on: 19 October 2010.