Neuro Flashcards
Classic features of NMO
Severe bilateral Optic neuritis and myelitis:
Loss of vision
Periocular pain
Dyschromatopsia
Disease associations with NMO
Sjogrens, SLE, Crohns, sarcoid
NMO vs MS
NMO = spinal cord and optic nerves
MS = sc, on AND brain
Imaging features of NMO on MRI spine
Longitudinally extension central lesions of >3 vertebral segments
Duration of MS symptoms to be considered an attack
At least 24 hours
With or without recovery, in absence of fever
Spinal cord lesion
Multifocal causes
Large segment causes
Multifocal causes: neoplastic, paraneoplastic,
Large segment causes:
Signs of MS on MRI (new Mcdonald criteria 2024)
- CVS - central vein sign - presence for a blood vessel through middle of an MS lesion
- PRLs - paramagnetic ring lesions - ring of iron around edge of active MS lesion
- Kappa free light chains in CSF (as accurate as oligoclonal band)
Dorsal column of spinal cord issue most likely to be caused by
Metabolic issue eg vitamin def such as b12 def
Alpha synucleinopathies
PD, LBD, MSA
Tau diseases
FTL
Alemtuzumab 12 monthly for 2 (or 3 doses), what % of people develop AI disease and what is AI D is most common?
30%, thyroiditis
1% of glomerulonephritis, eg similar to good pastures disease (can be very bad, worse than normal GP D)
MS treatments (mabs) and MOA
Natalizumab, monthly IV. A4 Integrin on T cells, prevents crossing BBB
Ocrelizumab - CD20 on b cells. Kills all middle aged b cells (not precursor or mature) 6 monthly IV
Issue with hypogammaglobulinaemia
Alemtuzumab - hard rest of Immune system. T and B cells CD52. 12 monthly, 5 days in a row, then next year 3 days in a row.
A virus that causes a cauda equina/conus medullaris picture
HSV2
Poliomyelitis affects which area of the spinal cord
Anterior segment
Presentation of West Nile Virus myelopathy
Subacute, months, progressive anterior cord syndrome, with high high fevers
But can be acute flavid paralysis
WNV can also cause encephalitis and meningitis
Mix of UMN and LMN sx, involving anterior horns
MND
What is MELAS?
Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke syndrome (MELAS)
Maternally inherited