Week 5 Flashcards
(41 cards)
Infection that often affects cranial nerves & other structures at brain base
Tuberculous meningitis (Mycobacterial infection)
3 bacterial meningitis species (~80% of cases)
Streptococcus pneumonia, Nisseria Meningiditis, H. Influenzae
Infection associated with Bell’s palsy
Neuroborreliosis (lyme disease)
Borrelia burgorferi
Account for 80% or more of viral meningitis
Enteroviruses
Herpetic encephalitis classical pathologic manifestation
HSV-1 infection of usually temporal lobes
Often associated with seizures
3 pathologies seen in viral encephalitis (and poliomyelitis)
Perivascular inflammation, microglial nodules, neuronophagia
Grocott (Silver) Stain associated with what infectious agent
Aspergillosis (fungus)
Three fungal CNS infectious agents
Aspergillosis, zygomycosis, cryptococcus neoformans (most common)
Multiple ring enhancing lesions
Toxoplasmosis (Toxoplasma gondii)
Heavily associated with brain abscesses
Common HIV encephalitis associated pathology
Multinucleated giant cells (not granulomatous)
Infectious agent with tropism for oligodendroglia
JC Virus (Polyoma virus) mediated Progressive Multifocal Leukoencephalopathy
Protein that stabilizes microtubules; associated pathological sign
Tau protein creates intracellular neurofibrillary tangles during CTE and AD
Amyloid precursor protein (APP) role in pathology of injury
1) Upregulated in neurons following injury
2) Cleavage at axon bulbs (post-injury) causes release of beta-Amyloid
Role of Calpain
Protease activated by calcium. Calpain cleaves Na inactivation gate in traumatic axonal injury
NaChO and significance
Sodium induced channelopathy
Increase in Na channels in axon membrane following mild traumatic brain injury
*Source of increased vulnerability to mTBI
Disease/disorder associated with TDP-43 protein aggregates
Frontotemporal dementia
Also ALS apparently
Classification of primary vs. secondary GBMs
Primary –> EGFR overexpression (gene amplification from loss of chrom 10)
Secondary –> IDH1 and p53 mutations (progression from lower grade astrocytomas)
Glomeruloid Tufts associated with what disease and what are they?
Associated with GBM (WHO IV)
Proliferation of cells around neurovascularization in middle of tumor
Common genetic profile of secondary GBM
- Often (60%) have p53 mutation; often have IDH1/IDH2 mutation; rarely have EGFR overexpression
- Usually progresses from an astrocytoma (grade II)
Common genetic profile of primary GBM
EGFR overexpression, rarely (<10%) have p53 mutation, rarely have IDH1/IDH2 mutation
Cancer occurring mainly in children and young adults
- Pilocytic astrocytoma (WHO I)
- Medulloblastoma
Rosenthal fibers and eosinophillic granules associated with what
Pilocytic astrocytoma
Corkscrew shaped fascicles of eosinhophilic cells
Biphasic cellular/histological architecture associated with what
Pilocytic astrocytoma
Compact architecture vs. cystic/spongy architecture adjacently
“Chicken-wire” and “Fried egg” appearance associated with what
Oligodendrogliomas
Chicken wire from branching capillaries
Fried egg from oligodendrites