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29 Cards in this Set

  • Front
  • Back
most common causes of acute meningitis/encephalitis
Enterovirus, Strep pneumo, Neisseria meningitis
most common causes of chronic meningitis/encephalitis
Mycobacterium, fungi, sarcoid, malignancy
most common causes of reccurent meningitis/encephalitis
Strep pneumo, HSV2
encephalopathy
altered consciousness with no evidence of inflammation in the CNS on imaging or CSF analysis (i.e. CSF white cell count <5/ml)
encephalitis
altered consciousness with no other cause identified and evidence of CNS inflammation on imaging or CSF analysis (i.e. CSF white cell sount 5/ml)
'virologically confirmed' encephalitis
Altered consciousness with a pathogen identified by culture or PCR of the CSF
meningism
only headache with neck stiffness and/or photophobia without evidence of altered consciousness and no evidence of inflammation on imaging or CSF analysis
purulent meningitis
meningism (headache with neck stiffness and/or photophobia) with a CSF white cell count >1000/ml or between 100 and 1000/ml with a predominance of PMN cells and a CSF:plasma glucose ratio <0.5 (or an unpaired CSF glucose <5mmol
'microbiologically confirmed' purulent meningitis
purulent meningitis with a pathogen identified by culture or PCR of the CSF or blood
aseptic meningitis
meningism in a conscious patient, with a normal CSF:plasma glucose ratio (>0.5) and either a CSF white cell count of 5-20 or 20-1000/ml with a lymphocyte predominance
'virologically confirmed' aseptic meningitis
aseptic meningitis with a viral pathogen identified by culture or PCR of the CSF
'microbiologically confirmed' TB meningitis
aseptic meningitis with Mycobacterium tuberculosis identified by culture or PCR of the CSF
differential diagnosis of meningitis and encephalitis
non-infectious diseases
viral
bacterial
fungal
mycobacterial
parasites
non-infectious causes of aseptic meningitis
lymphomatous meningitis (malignancy), connective tissue disease (i.e. lupus), sarcoidosis, Behcet's syndrome, drugs (NSAIDS, antibiotics), post-vaccination/post-infectious virus
enteroviral meningitis -- clues
exanthem, myopericarditis, conjunctivitis, hand-foot-mouth disease, herpangina, pleurodynia
enterovirus -- risk factors
fecal-oral (swimming in sewage contaminated water)
season (summer-fall in temperate climates, year-round in tropical climates)
infants, young children w/o immunity
congenital or acquired immune deficiency
chronic enteroviral meningoencephalitis in agammaglobulinemia (CEMA) -- symptoms
unique clinical syndrome
headache, seizures, hearing loss, coma, weakness, ataxia, paresthesias, loss of cognitive skills
initial signs/symptoms of CNS mumps
fever 72-96 hrs, vomiting, headache, salivary gland swelling, meningismus, lethargy
[abdominal pain, seizures]
Features of HSV encephalitis
abnormal CSF (protein>40 mg/dl, glucose<50%, CSF leukocytes, erythrocytes), focal EEG/brain/CT scan
West Nile Virus: % asymptomatic/fever/neuroinvasive disease
80% asymptomatic
20% West Nile fever
<1% Neuroinvasive disease: Aseptic meningitis, Meningoencephalitis, Acute flaccid paralysis
(Rarely movement disorders, cranial neuropathy, optic neuritis)
Features of CMV encephalitis
HIV & transplant patients
signs: acute deterioration in mental status (4 weeks)
benign CSF except elevated protein
nearly 100% PCR-positive, rarely culture-positive
periventricular inflammation or focal hypodensities
Subacute sclerosis panencephalitis (SSPE)
associated with measles
insidious, personality changes, periodic axial myoclonic jerks with recurrent falls, then generalized rigidity with unresponsiveness
Features of VZV encephalitis
55% preceding rash
50% co-morbidities
disorientation, confusion, meningeal signs, focal neurological signs, apathy, cranial nerve palsy
CSF mod. elevated, low glucose & protein
JC Virus (Polyoma virus)
seroconversion in 50% by age 6 , 90% by middle age
kidney harbors virus
disease in immunocompromised- due to reactivation
Progressive Multifocal Leukoencephalopathy (PML) -- pathogenes
due to cytolytic replication of JC polyomavirus in the oligodendrocytes of the brains of immunodeficient patients; the oligodendrocytes synthesize the myelin protein that sheaths the axons of neurons in the CNS --> demyelinating
Progressive Multifocal Leukoencephalopathy (PML) -- symptoms
no "usual" course; symptoms depend on which areas of brain are affected
-- focal motor and sensory deficits
-- gait abnormalities
-- speech and language disturbances
-- cognitive disorders
-- headache
-- visual impairment
spongiform encephalopathy -- cause; name
Transmissible protein (prions, no nucleic acid content of the infectious particle) can cause a disease known as Creutzfeldt Jakob Disease (CJD).
spongiform encephalopathy -- transmission
Can be transmitted by infected cattle (Bovine spongiform) new variant CJD, contaminated neurosurgical instruments (iatrogenic CJD), sporadic mutations, and genetic
normal vs. pathogenic prions
Normal cellular prions are monomeric, non infectious, soluble in mild detergents.
Pathogenic prion protein aggregates in sheets, is infectious and not soluble and forms fibrils seen on EM of brain.