Rest of acute neuro Flashcards
A 62-year-old woman presents back pain and difficulty walking. On examination there is increased tone and hyper-reflexia in both legs. She has not opened her bowels or passed urine for the previous day. She has a past medical history of breast cancer, diagnosed two years earlier. Which is the most likely diagnosis?
Spinal cord compression
A 20-year-old woman presents with pins and needles in both legs. Her symptoms rapidly progress over 4 days to include lower extremity weakness to the point that she is unable to mobilise her lower extremities. She reports gastrointestinal symptoms 2 weeks ago. Lumbar puncture reveals mildly elevated protein with no cells and normal glucose.Given the most likely neurological diagnosis which organism is most likely to have caused the gastroenteritis?
Salmonella Campylobacter Jejuni E. Coli 0517 Rotavirus Entamoeba histolytica
Campylobacter jejuni
Define GBS
Acute autoimmune demyelinating polyneuropathy
affecting the PNS
What is the pathophysiology of GBS
AI process attacking myelin sheath or Schwann cells in sensory and motor peripheral nerves
Cause of GBS?
Unknown but 2/3rds preceded by an URTI or gastroenteritis 2-3 weeks previously
Which type of cell produces myelin
Schwann cells
What are the viral causes of GBS (5)
CMV, EBV, HepB/C, HIV
What are the bacterial causes of GBS (2)
campylobacter jejuni, mycoplasma
What is the triad in Miller-Fischer syndrome and the one thing it is without
ophthalmoplegia, areflexia & ataxia but NO muscle weakness. In Miller-Fisher syndrome there are antibodies against a specific ganglioside (GQ1b)
What is the triad of: ophthalmoplegia, areflexia & ataxia but NO muscle weakness known as
Miller-Fischer syndrome
Signs of GBS (4)
Hypotonia
Flaccid paralysis ( = weakness/paralysis & ↓ muscle tone)
Altered sensation/numbness
Fasciculations
Symptoms of GBS (6)
Peripheral neuropathy
Progresses acutely
Ascending paraesthesia & pain
Symmetrical limb weakness
Can also cause facial nerve palsy
Can also have autonomic symptoms (urinary retention, ileus)
If this progresses to resp. paralysis, patients might need ventilatory support
Ix for GBS (4)
Nerve conduction studies
Lumbar puncture
Spirometry
Bloods
How often should you perform spirometry in a GBS patient
Every 6 hours
What do you see in the nerve conduction study of a GBS patient
Decreased nerve conduction
What do you see in the lumbar puncture of a GBS patient (3)
Albuminocytological dissociation (a hallmark of demyelinating polyneuropathies)
↑ protein (reflects CNS inflammation)
normal glucose & cell count (due to no infection)
What are you looking for in the bloods of a GBS suspected patient
Anti-ganglioside AB’s (Miller-Fischer variant)
Which AB is present in Miller-Fischer variant GBS
anti-ganglioside
Define hydrocephalus
Excessive accumulation of CSF in the ventricular
system in the brain.
Epidemiology of hydrocephalus
Bimodal distribution (affects the young & elderly)
Pathophysiology of hydrocephalus
Bc you have excess CSF, the ICP increases. CSF also permeates through the ependymal lining into the periventricular white matter. This results in white matter damage and gliotic scarring.