what is viral meningitis cause by - Mumps, enterovirus
wht is encephalitis caused by - herps reactivation
wht is brain abscess caused by - streptococal, anaerobes
waht is facial palsies caused by - VZV - reactivation
transissable spongiform encephalopathies - prions
waht is CJD a type of - transmissible spongiform encephalopathies
wt causes conjunctivitis, HSV, clamydia trachomatis, Adenovirus
wt causes karetinits -HSV, Clamydia trachomatis
wt causes retinitis - CMV - esp inAIDs
Ability to outline key aspects of:
Acute Meningitis: Clinical appearance, epidemiology, etiology, treatment approaches.
Brain Abscesses & Encephalitis: Aetiology, clinical presentation, treatment approaches.
Creutzfeldt-Jakob Disease (CJD): Classification, pathogenesis, routes of transmission, epidemiology.
Key Eye Infections: Conjunctivitis, keratitis, retinitis.
Mechanisms for organism entry into the CNS include:
Contiguous Spread: Infection from sinuses, ear, mastoid, or face.
Trauma: Direct inoculation from injuries.
Hematogenous Spread: Via the bloodstream
via nerves.
Meningitis: Inflammation of the meninges.
Encephalitis: Inflammation of the brain substance.
Common symptoms include:
Fever & Stiff Neck
Photophobia
Headache
Vomiting
Irritability & Drowsiness
Viral Meningitis:
More common, often benign, usually leads to complete recovery.
Common viruses: Enteroviruses, Mumps virus.
Bacterial Meningitis:
Less common but more severe, can lead to mortality and morbidity.
Common bacteria:
Neisseria meningitidis
Streptococcus pneumoniae
Haemophilus influenzae.
Bacterial vs. Viral:
Presence of neutrophils, glucose levels, protein concentrations, and culture results vary.
large decrease in glucose and large increase in protein in bacterial meningitis
Increased neutrophils suggest bacterial; lymphocytes indicate viral causes.
Focus on the big three: NHS - medical emergency
Neisseria meningitidis
Haemophilus influenzae (specifically capsule type b)
Streptococcus pneumonia
Most common and severe form, particularly in children (<5) and young adults (15-20).
Characterized by:
Meningococcal Meningitis with a rash, purpura, non blanching on tumbler test
clusters - It's carried in the nose/throat of some people without symptoms, and can spread via coughing, sneezing, or kissing.
Various capsule types with vaccines available for types A, C, and B.
case b more popular in uk
transmittion via respiratory droplets, more common in winter
The virus hat cause bacterial meningitis can also cause septicaemia. Septicaemia can occur with or without meningitis.
Public health responses to clusters include:
Antibiotic prophylaxis.
Vaccination strategies targeting types A and C, with newer types for B.
Tetravalent Vaccine: Covers serotypes A, C, Y, & W135. but not B
Men C conjugate vaccine included in UK childhood immunization schedule.
Men B vaccine more common in uk
Caused by Streptococcus pneumoniae, often seen in older populations or post-head trauma.
Resistance to penicillin is a growing problem
prevention - vaccines
Mainly from Haemophilus influenzae type b; children 1-5,
significantly reduced incidence after the introduction of HIB vaccine.
prevention - HIB vaccine and Antibiotic prophylaxis for close contacts important for management.
Caused by Mycobacterium tuberculosis.
Prolonged treatment with anti-TB medications is required; infection usually originates from lungs.
The most common type of meningitis; typically benign with complete recovery.
CSF- shows no bacteria but with Enterovirus (Coxsackie, Echovirus), VZV, and Mumps.
PCR to identify virus
no specific treatment
Lumbar puncture (LP) checks for:
Intracranial pressure
CSF examination: WBC cell counts, glucose and protein chemistry, staining films, cultures, PCR.
no specfic treatment for viral
Urgent Management:
Immediate antibiotic therapy; administer benzyl penicillin for suspected meningococcal disease.
cefotaxime or ceftriaxone for unknown bacterial causes.
Inflammation of brain substance; primarily caused by the herpes simplex virus (HSV-1) in temporal lobe brain as a reactivation infection
Symptoms include stroke-like signs, memory loss, behavioral changes, seizures.
Aciclovir for treatment
Enteroviruses (summer-autumn occurrences).
Arboviruses (mosquito-borne, e.g., West Nile).
Rabies: 100% fatal without intervention; spread from animal bites.
Caused by bacteria - streptococi, anaeobes
Focal (specifc) infection characterized by a collection of pus, often related to: otitis media, sinusitis, dental abscess, or trauma, endocarditis
Symptoms similar to encephalitis
management typically requires surgical intervention along with antibiotics.
Cranial nerve palsies occur when one or more of the 12 cranial nerves, which connect the brain to the head, face, and neck, malfunction, causing a range of symptoms like double vision, droopy eyelids, or facial weakness.
facial (7) nerve plasies - VZV reactivation (Ramsay Hunt Syndrome).
symptoms - facial paralysis and shingles rash
misfold proteins causing normal proteins in the brain to misfold as well
Unconventional 超脫 infectious agents, tiny, lacking nucleic acid;
resistant to heat, disinfection, UV radiation, sterilization techniques.
Long incubation periods with no immune response observed.
Includes Creutzfeldt-Jakob Disease (CJD); may be genetic, sporadic零落, or infectious.
Transmission by abnormal folding of prion proteins (PrP).
abormal prions inducing other normal proteins in the brain to misfold, leading to progressive brain damage.
due to its sporadic characteristic, genetic mutation in PrP, infectious person to person
caused by abnormal folding of prions, lead to brain degeneration → dementia, memory loss
Sporadic/spontaneous CJD (sCJD) – ~85% of cases
Happens randomly, without known cause
Hereditary CJD – ~10–15%
Mutation in the PRNP gene
Acquired CJD – very rare
Includes:
Variant CJD (vCJD) – linked to mad cow disease (bovine spongiform encephalopathy)
Iatrogenic CJD – via medical procedures (e.g., contaminated instruments)
Instruments used on the brain/spinal cord can carry prions.
Neurosurgical tools and brain electrodes have caused transmission.
Prions are very sticky — they stick to metal and resist sterilization.
In variant CJD (linked to mad cow disease), prions can be found in lymphoid tissue, including tonsils.
This means even a tonsillectomy could pose a transmission risk.
There have been documented cases of vCJD being spread through blood transfusion.
This is why donor screening is so strict in some countries (e.g., UK restrictions on donating if you lived there in the 1980s–90s).
In the past, growth hormone was taken from cadaver brains, which spread prions to children.
This is no longer done — now it's made synthetically.
Prions are highly concentrated in nervous tissue.
So even tissues with nerves — like gingival tissue (gums) or dental pulp (inside teeth) — are considered potentially risky.
There’s concern about dental procedures like root canals.
Files used in root canals may come into contact with nerve tissue.
Because prions are resistant to standard sterilization, there’s concern that they could stay on instruments and infect another patient.
Hard to quantify risk → It's rare, and we can't easily test for prions.
Many concerns are precautionary rather than based on frequent real-world cases.
But because prion diseases are fatal and untreatable, even small risks are taken very seriously.
Focus on conjunctivitis, keratitis, retinitis.
Infectious agents include:
Bacteria and adenovirus; highly infectious and usually bilateral.
HSV can lead to karatitis
Chlamydia trachomatis (STI) through auto-inoculation, often maternal transmission.
Infection of the cornea
HSV repeated reactivation leading to scarring
Chlamydia trachomatis (bacteria) associated with trachoma. (eye disease)
Commonly associated with CMV, especially in AIDS patients.
Toxoplasmosis in utero related to maternal infections from cat feces or undercooked meat,
presenting with visual disturbances.