Difference between revisions of "Neuropathology"

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==Weird stuff==
==Weird stuff==
==Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)==
==Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)==
General:
===General===
*Autosomal dominant disorder - the name implies.<ref name=pmid19174371>PMID: 19174371.</ref>
*Autosomal dominant disorder - the name implies.<ref name=pmid19174371>{{Cite journal  | last1 = Tikka | first1 = S. | last2 = Mykkänen | first2 = K. | last3 = Ruchoux | first3 = MM. | last4 = Bergholm | first4 = R. | last5 = Junna | first5 = M. | last6 = Pöyhönen | first6 = M. | last7 = Yki-Järvinen | first7 = H. | last8 = Joutel | first8 = A. | last9 = Viitanen | first9 = M. | title = Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients. | journal = Brain | volume = 132 | issue = Pt 4 | pages = 933-9 | month = Apr | year = 2009 | doi = 10.1093/brain/awn364 | PMID = 19174371 }}
</ref>
*Cases strokes in 40-50 year-old.
*Cases strokes in 40-50 year-old.
*Characteristic MRI findings - present in asymptomatic individuals with mutation.
*Characteristic MRI findings - present in asymptomatic individuals with mutation.


Etiology:
===Etiology===
*Mutation of ''Notch 3'' gene.<ref name=pmid15537516>PMID: 15537516.</ref>
*Mutation of ''Notch 3'' gene.<ref name=pmid15537516>{{Cite journal  | last1 = Kalaria | first1 = RN. | last2 = Viitanen | first2 = M. | last3 = Kalimo | first3 = H. | last4 = Dichgans | first4 = M. | last5 = Tabira | first5 = T. | title = The pathogenesis of CADASIL: an update. | journal = J Neurol Sci | volume = 226 | issue = 1-2 | pages = 35-9 | month = Nov | year = 2004 | doi = 10.1016/j.jns.2004.09.008 | PMID = 15537516 }}</ref>


Diagnosis:
===Diagnosis===
*Proven ''Notch3'' mutation.
*Proven ''Notch3'' mutation.


Histology:
===Histology===
*Electron microscopy (skin biopsy):
*Electron microscopy (skin biopsy):
**Granular osmiophilic material (GOM).
**Granular osmiophilic material (GOM).

Revision as of 03:36, 30 June 2010

Neuropathology is the bane of many anatomical pathologists in teaching hospitals... 'cause they have to fill in for the neuropathologist when he or she is on vacation.

This article is an introduction to neuropathology. There are separate articles for brain tumours, the pituitary gland and muscle pathologies.

Normal histology

  • Neurons.
    • Large cells.
    • Has prominent nucleolus.
  • Glial cells.
    • Oligodendrocyte - looks like a fried egg on H&E (clear cytoplasm, central nucleus).
  • Astrocyte.
    • Close to blood vessels.
    • Have processes.
    • Form blood-brain barrier.
  • Microglia - macrophage of the brain (derived from monocyte).
    • May be large.
    • May have vesicles.

Hippocampus

Image: Hippocampus - frontal section (WP)

Orientation:

  • CA3 - superior
  • CA1 - inferior
  • CA3 - in between CA3 and CA1
  • Dentate gyrus (DG) points lateral and inferior and toward CA1.


CA1 - weak link, dies in ischemia, affected by hypoglycemia.[1]

Histopathology

  • Reactive astrocytes.
    • eosinophilic cytoplasm.
    • peripheral nucleus.
    • well-defined cell border.
    • many branching processes.

Architecture

  • Rosette = circular/flower-like arrangement of cells[2]
  • Pseudorosette = circular/flower-like arrangement of cells with blood vessel at the centre[2]
  • Rosenthal fibres = worm-like or corkscrew-like eosinophilic bodies.
  • Pseudopallisading

Notes: Good set of articles - [3]

Mass

In HIV/AIDS patients... mass on CT if infection:

  • Toxoplasmosis - most common.[4]

Ring enhancing lesion (DDx) - mnemonic MAGICAL DR:[5]

  • Metstasis.
  • Abscess.
  • Glioblastoma.
  • Infarct.
  • Contusion.
  • AIDS-related.
  • Lymphoma + HIV assoc. disease (toxoplasma).
  • Demyelination (e.g. multiple sclerosis).
  • Resolving hematoma.

Alcohol & CNS

Pathology:[6]

  • Morel's laminar sclerosis
  • central pontine myelinolysis
  • Wernicke's encephalopathy
    • Mnemonic WACO:
      • Wernicke's.
      • Ataxia.
      • Confusion, confabulation -- Korsakoff.
      • Ocular Sx (CN IV palsy).
    • Cause: thiamine deficiency.
  • Mammillary body shrinkage.[7]

Non-tumour

Acute disseminated encephalomyelitis

General

  • Thought to be autoimmune.
  • May mimic multiple sclerosis.
  • Abbreviated "ADEM".

Diagnosis

  • Need to r/o infection (with lumbar puncture).
  • No old plaques on imaging (MRI).

Micro

  • Spares subcortical fibres (???)

Tx

  • Steroids.
  • Plasmapheresis.

DDx

  • Multiple sclerosis

Cysts

General:

  • All are "benign", but some may be fatal due to spatial constraits.
  • Colloid cyst[8]
    • columnar epithelium.
  • Arachnoid cyst - considered precursor of meningioma.
    • psammoma bodies.
    • clumps of cells.
    • whorled pattern.
  • Dermoid cyst.
    • skin + adnexal structures.
    • ... think of ovarian dermoid.
  • epidermoid.
  • choriod cyst.
    • ?
  • neuroenteric cyst.
  • epithelial cyst.

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:[9]

  • 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.[10]
    • Alpha-synuclein is implicated in a number of neurodegenerative diseases.[11]

Brain tumours

Main article: Neuropathology tumours

Tumours are a big part of neuropathology.

Paediatric pathology

Joubert syndrome

  • Malformation of the cerebellar vermis.[12]

Epidemiology

  • Autosomal recessive - mutation in a number of genes including NPHP1, AHI1, and CEP290.[12]

Histiocytoses

Features of histiocytoses:[13]

Histologic features EM features CD68 S-100 CD1a
Macrophage epithelioid cells, giant cells - + - -
Erdheim-Chester disease Touton giant cells - + +/- -
Rosai-Dorfman Emperipolesis - + + -
Langerhans-histiocytosis Reniform nuclei,
eosinophilic cytoplasm 		Birbeck granules + + +

Stroke

Gross

  • Soft/mushy brain.
  • Older infarcts.
    • A "roof" is present - a thin submeningeal layer is preserved by the CSF.[14]
      • "Roof" is absent in trauma.
    • Cavity - in older infarcts.
      • Multiple sclerosis does not cavitate.

Weird stuff

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

General

  • Autosomal dominant disorder - the name implies.[15]
  • Cases strokes in 40-50 year-old.
  • Characteristic MRI findings - present in asymptomatic individuals with mutation.

Etiology

  • Mutation of Notch 3 gene.[16]

Diagnosis

  • Proven Notch3 mutation.

Histology

  • Electron microscopy (skin biopsy):
    • Granular osmiophilic material (GOM).

See also

References

  1. ↑ B. August 2009.
  2. ↑ 2.0 2.1 PMID 16551982
  3. ↑ http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=PureSearch&db=PubMed&details_term=Neuropathology%20for%20the%20neuroradiologist
  4. ↑ MUN. Feb 3, 2009.
  5. ↑ TN2005 NS7.
  6. ↑ http://www.journals.elsevierhealth.com/periodicals/ycdip/article/S0968-6053(07)00035-X/abstract
  7. ↑ Shear PK, Sullivan EV, Lane B, Pfefferbaum A (November 1996). "Mammillary body and cerebellar shrinkage in chronic alcoholics with and without amnesia". Alcohol. Clin. Exp. Res. 20 (8): 1489-95. PMID 8947329. http://www3.interscience.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0145-6008&date=1996&volume=20&issue=8&spage=1489.
  8. ↑ MUN. 11 Mar 2009.
  9. ↑ TN06 PS19
  10. ↑ PMID 18825660
  11. ↑ PMID 18855701
  12. ↑ 12.0 12.1 http://www.ninds.nih.gov/disorders/joubert/joubert.htm
  13. ↑ Sternberg Surg. Path. P.479.
  14. ↑ MUN. 16 December 2009.
  15. ↑ Tikka, S.; Mykkänen, K.; Ruchoux, MM.; Bergholm, R.; Junna, M.; Pöyhönen, M.; Yki-Järvinen, H.; Joutel, A. et al. (Apr 2009). "Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients.". Brain 132 (Pt 4): 933-9. doi:10.1093/brain/awn364. PMID 19174371.
  16. ↑ Kalaria, RN.; Viitanen, M.; Kalimo, H.; Dichgans, M.; Tabira, T. (Nov 2004). "The pathogenesis of CADASIL: an update.". J Neurol Sci 226 (1-2): 35-9. doi:10.1016/j.jns.2004.09.008. PMID 15537516.

External links

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