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18 Cards in this Set

  • Front
  • Back
What is ephaptic conduction?
After nerve injury, increased spontaneous firings from newly formed nerves form. Atypical connections develop between neighboring neurons leading to "cross-talk" or ephaptic conduction"
What are the imaging McDonald's Criteria?
3 out of the following:
1) 1 Gd enh lesion or 9 T2 hyperintense lesions
2) 1 juxtacortical
3) 1 infratentorial
4) > 3 periventricular
What are Dawson's fingers?
ovoid shaped, abutting ventricles about 3 mm in size, perpendicular to ventricles. These result from T cell damage along the venules that are perpendicular to the ventricles.
What are the 4 subtypes of MS?
Relapsing Remitting
Progressive Relapsing
Secondary Progressive
Primary Progressive
What percentage of patients have pleoctyosis?
more than 1/3 of patients
What percentage of patients have positive oligoclonal bands?
90% in definite MS *at some point in disease
**Usually they have at least 2 OCBS
How often do Gd Enhancing lesions last in MS?
4-6 weeks
What is the maximum dose of Baclofen
80 mg/day divided into 4 doses
What is the maximum dose of Tizanidine?
36 mg daily
SE: somnolence,asthenia, dry mouth, liver toxicity rare, orthostatic hypotension, careful in elderly and renal impairment
What is the pop sensation correlate to anatomically during a lumbar puncture?
Puncture of the ligamentum flavum
What are the layers you enter with your spinal needle?
1) Skin/Subcutaneous tissue
2) Supraspinous ligament
3) Interspinous ligament
4) Ligamentum flavum
5) Epidural space
venous plexus
6) Arachnoid
7) Subarachnoid
What percentage of patients with MS present with optic neuritis?
25%
What is balo's concentric sclerosis?
MS variant with bands of demyelinating and remyelinating disease
What is Schilder's disease?
variant of MS with aggressive disease course, deafness or cortical blindness and demyelination involving entire hemisphere or corpus collosum
What is Cogan's syndrome?
interstitial keratitis + inner ear abnormality
What is Alport's syndrome?
sensorineural hearing loss + interstial nephritis X linked
What is Usher's syndrome?
sensorineural hearing loss+ retinitis pigementosa (autosomal recessive)
What are the significant pathologic findings in this patient with susppected PML?
Bizzare astrocytes, lipid-laden ballooned oligodendrocytes with ground glass inclusions