11 - Neuropathology Flashcards
The CNS is normally sterile so how do microorganisms gain entry to cause infections?
- Direct spread (from middle ear, basal skull fracture, even through ethmoid bone)
- Blood bourne (in sepsis or infective endocarditis)
- Iatrogenic (post neurosurgery, ventriculoperitoneal shunt, lumbar puncture)
What is the pathophysiology of acute meningitis and what are the causative organisms?
- Inflammation of the leptomeninges (pia and arachnoid) +/- a non blanching rash (if meningococcal septicaemia)
- Most common in 5-30, rarely HiB due to vaccine
What is chronic meningitis?
- Caused by M. tuberculosis and lasts at least 4 weeks
- Granulomas
- Meningeal fibrosis
- Cranial nerve entrapment in fibrosis so facial nerve palsie and headaches
- Bilateral adrenal haemorrhage (Waterhouse-Friederichsen
syndrome) can occur as a complication
What are some of the complications of meningitis?
What is the pathophysiology of encephalitis?
- Usually viral
- Inflammation of brain parenchyma not meninges (but can be a complication of meningitis)
- Virus kills neurones causing inflammation and presence of intracellular viral inclusions
- Often get lymphocytes infiltrating
What are some of the common organisms causing encephalitis?
Different viruses affect different lobes. As chronic inflammation usually presents as headaches. Often self-limiting
Temporal lobe: Herpes viruses (most common)
Spinal cord: Polio (now eradicated)
Brainstem: Rabies (very rare)
What is a prion and how can it cause disease?
- Normal protein needed for synaptic function
- PrP can become mutated themselves (sporadic) or familial or ingested to PrPSC
- PrPsc interacts with normal prions and cause them to aggregate together causing cell death of grey matter and causes brain to have a spongiform appearance
What virus is this?
CMV - can see ‘owl eyes’ which are inclusions of the virus replicating
Why are mutated prions so ‘dangerous’ and more than certain to cause disease?
- PrPsc can convert PrP into itself (i.e. induce a conformational change) by protein-protein interactions alone
- PrPsc is extremely stable (resistant to disinfectants, irradiation) and not susceptible to immune attack as it is essentially a ‘self’ protein
What are some spongiform encephalopathies caused by prions?
- Scrapie in sheep
- BSE in Cows
- Kuru in tribes of New Guinea (ingested)
- vCJD
What is variant CJD and how does it differ to classic CJD?
- Strongly linked to BSE through ingestion of prions e.g eating spinal cord of cow from butchers
- Essential difference compared to classical CJD is that there seems to be a much higher prion load associated with earlier age at death and more prominent psychiatric symptoms (e.g seizures and vision loss)
- Classic CJD is a form of dementia
Are prion diseases infections?
Unclear as does not completely fulfil all of Koch’s postulates as found in healthy organisms!!!
What is the definition of dementia and what are the different types?
Acquired global impairment of intellect, reason and personality without impairment of consciousness (delirium would affect consciouness)
What are the different categories of Alzheimer’s disease?
- Early/Late
- Sporadic/Familial
- Most are late sporadic
What is the pathophysiology behind Alzheimer’s disease?
- Loss of cortical neurones due to neuronal damage by neurofibrillary tangles and amyloid plaques. Leads to cortical atrophy and decreased brain weight
Neurofibrillary tangles: intracellular twisted filaments of Tau protein that normally binds to microtubules. Hyperphosphorylation of tau is thought to lead to tangle formation and form a plaque
Senile Plaques: foci of enlarged axons, synaptic terminals and dendrites. Amyloid deposition in centre of tau plaque associated with vessels. (cotton wool balls)