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OPT CNS
Term | Definition |
---|---|
1. thrombotic occlusion 2. embolic occlusion 3. vascular rupture | 3 processes of cerebrovascular diseases |
functional hypoxia | low partial pressure of O2, impaired O2 carrying capacity are some examples of this |
ischemia | result of tissue hypo perfusion caused by hypotension and vascular obstruction; form of hypoxia |
global cerebral ischemia | widespread ischemic injury with generalized reduction of cerebral perfusion below 50 mm Hg pressure |
focal cerebral ischemia | due to a cerebral occlusion that causes focal ischemia -{embolic infarcts are the most common} |
paradoxical emboli | embolus from venous circulation crosses to arterial through atrial or ventricular septal defect |
cerebral infarcts | most commonly in areas supplied by the middle cerebral artery |
transient ischemic attack (TIA) | precedes a cerebral infarct, neurologic dysfunction caused by self-limited episodes of obstruction |
primary brain parenchymal hemorrhage | spontaneous intraparenchymal hemorrhages; hypertension is underlying cause |
subarachnoid hemorrhage and saccular aneurysms | acute increases in intracranial pressure; can cause a rupture of a saccular (berry) aneurysm |
chronic traumatic encephalopathy (CTE) | trauma associated with degeneration of the brain; in NFL players |
contusions | brain hits skull during head injury; rapid tissue displacement and hemorrhage |
diffuse axonal injury | widespread injury to axons in brain due to movement of one area of the brain relative to another |
concussion | reversible altered consciousness from head injury in absence of contusion; transient neurologic issues |
epidural hematoma | middle meningeal artery vulnerable to injury; neurosurgical emergency |
subdural hematoma | between dura and brain; in babies and old people |
epidural abscesses | adjacent to site of infection, forms pus in a new cavity |
subdural empyema | infections in skull or sinuses, can spread and form pus in a normal cavity |
meningitis (leptomeningitis) | inflammatory process of leptomeninges in subarachnoid space; called {meningoencephalitis} if it goes to brain |
acute pyogenic meningitis (bacterial meningitis) | smear can be cultured from CSF; patients show signs of systemic infection |
aseptic meningitis | infection of mycobacteria or spirochetes |
neurosyphilis | tertiary stage of disease, loss of mental and physical functions -paretic syphilis- invasion to brain |
tabes dorsalis | wasting of peripheral nerves in dorsal root so impaired proprioception |
Charcot joints | loss of pain sensation leading to skin and joint damage in tertiary syphilis |
brain abscesses | almost always bacterial infection; destructive lesions |
viral encephalitis | almost always associated with the meninges so aka {meningoencephalitis} |
progressive multifocal leukoencephalopathy | caused by JC virus in AIDS patients; demyelinates oligodendrites |
prion disease (spongiform encephalopathies) | microscopic vacuolation in neurons; abnormal forms of prion protein |
scapie | prion disease in sheep |
bovine spongiform encephalopathy | prion disease in cattle |
Creutzfeldt-Jakob Disease | rare prion disease of rapid dementia in people over 70 |
variant Creutzfeldt-Jakob disease | aka 'Mad Cow Disease'; acquired in younger people from BSE |
demyelinating diseases | normal myelin is broken down; includes MS and progressive multifocal leukoencephalopathy |
multiple sclerosis (MS) | autoimmune demyelinating disease; unilateral visual impairment is often first sign |
dysmyelinating diseases | metabolic disorders of abnormal myelin aka {leukodystrophy} |
leukodystrophies | inherited diseases of mutations of normal myelin formation or turnover |
thiamine deficiency | causes Wernicke-Korsakoff syndrome |
Wernicke encephalopathy | confusion, eye movements, and ataxia; thiamine deficiency |
Korsakoff syndrome | thiamine deficiency that progresses to this irreversible condition, memory disturbances |
Wernicke-Korsakoff syndrome | thiamine deficiency in alcoholics |
Vitamin B12 deficiency | leads to {pernicious anemia} and subacute combined degeneration of the spinal cord |
dementia | development of memory impairment and cognitive deficits, decreasing functional ability |
Alzheimer disease | most common cause of dementia in elderly |
beta amyloid | peptide that accumulates in brain, initiates chain of events that results in AD |
tau | hyperphosphorylated by beta amyloid; redistributes and forms tangles |
plaques | extracellular lesion of AD |
neurofibrillary tangles | intracellular lesion of AD |
Parkinson Disease | masked facies, stooped posture, slow movement and tremor; damage to dopaminergic neurons |
Lewy body | diagnostic of Parkinson Disease; inclusion of alpha-synuclein for synaptic transmission |
Huntington Disease | auto-dominantly inherited disease, jerky movements and dementia; trinucleotide repeat in Huntington gene |
amyotrophic lateral sclerosis (Lou Gehrig's Disease) | death of low motor neurons in spinal cord and upper motor neurons in cortex; superoxide dismutase mutation -death by respiratory infection |
glioma | tumors of brain parenchyma that resemble glial cells |
astrocytoma | most common group of primary CNS tumors |
medulloblastomas | in children and in cerebellum, highly malignant; kids with Nevoid Basal Cell Carcinoma |
meningioma | benign adult tumors, usually attached to dura |
tuberous sclerosis | auto-dominantly inherited syndrome of hamartomas (tubers) that cause seizures |
Von Hippel Lindau Disease | auto-dominantly inherited disorder of hemangioblastomas on CNS structures; can develop renal cell carcinoma |