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257 Cards in this Set

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SCALP

Skin - Connective Tissue - Aponeurotica - Loose Areolar CT - Pericranium (periosteum)
Anterior Fossa
Contains Frontal Lobe, divided from the middle fossa by the lesser wing of sphenoid bone
Middle Fossa
Contains Temporal lobe, divided from the posterior fossa by the petrous ridge of the temporal bone as well as by a sheet of meninges - Tentorium Cerebelli
Posterior Fossa
Contains the cerebellum and brainstem
Falx Cerebri
Flat sheet of Dura that is suspended from the roof of the cranium and separates the right and left cerebral hemispheres, running in the interhemispheric fissure
Tentorium Cerebelli
Tent like sheet of Dura that covers the upper surface of the cerebellum
Supratentorial
Above the Tentorium Cerebelli
Infratentorial
Below the Tentorium Cerebelli
Tentorial Notch
Also known as Tentorial Incisure, narrow opening in the tentorium cerebelli which the midbrain passes through. At the level of CNIII and the Interpeduncular fossa.
Virchow-Robin Space
where pia surrounds initial portion of each blood vessel as it penetrates the brain surface forming a perivascular space and then fuses with the blood vessel wall
Epidural Space
between dura and skull; contains the middle meningeal artery
Middle Meningeal Artery

Enters skull through the foramen spinosum and runs in the epidural space between the Dura and the skull

Subdural Space
Potential space between the inner layer of Dura and the loosely adherent arachnoid
Bridging Veins
Traverse the subdural space and drain the cerebral hemispheres and pass through the subdural space en route to several large Dural venous sinuses
Dural Sinuses
Large venous channels that lie enclosed within the two layers of Dura, Dural sinuses drain blood mainly via the sigmoid sinuses to reach the internal jugular vein.
Subarachnoid Space
CSF filled space between arachnoid and pia, also major arteries of the brain travel within the subarachnoid space and then send smaller penetrating branches inward through the pia
Epidural Fat
In spinal canal only layer between the Dura and the periosteum
Ependymal cells
line the ventricles
Choroid Epithelial Cells
Blood vessels of the choroid plexus are lined with ependymal like cuboidal cells called Choroid Epithelial Cells
Lateral ventricles
one in each cerebral hemisphere
Anterior (frontal) horn: anterior to foramen of Monro and extends to frontal hemisphere
Body: Posterior to foramen of Monro; within frontal and parietal lobe
Atrium (trigone): area of convergence of the occipital horn, and the body of the lateral ventricle
Occipital (posterior) horn: Extends from the atrium posteriorly into the occipital lobe
Temporal (inferior) horn: Extends from the atrium inferiorly into the temportal lboe
Third ventricle
within the thalamus and hypothalamus
Fourth ventricle
within the pons, medulla, and cerebellum
General Flow of CSF
Lateral Ventricles ---(foramen of monro)--> Third Ventricle ---(cerebral aqueduct/aqueduct of Sylvius)---> fourth ventricle ----(foramina of Lushka and foramen of Magendie) --> outsideeee world
Normal total CSF volume adults
150cc
Rate of CSF production
20cc/hour (500cc/day)
Cisterns
Areas where subarachnoid space widens in a few areas to form larger CSF collections called Cisterns
Ambient Cistern
located lateral to the midbrain
Quadrigeminal Cistern
posterior to the midbrain, beneath the posterior portion of the corpus callosum (quad bc four bumps of superior and inferior colliculi)
Interpenduncular Cistern (Interpeducular fossa)
located on the ventral surface of the midbrain between the cerebral peduncles
Prepontine Cistern
located just ventral to the pons, contains the basilar artery and the 6th nerves as they ascend from the pontomedullary junction along the cilvus
Cisterna Magna (cerebellomedullary cistern)
largest cistern; located beneath the cerebellum near the foramen magnum
Lumbar Cistern
located in the lumbar portions of the spinal column, contains the cauda equina and is the region from which CSF is obtained during a lumbar puncture or spinal tap
What substances permeate readily across the cell-membrane of the blood-brain and blood-CSF barriers
O2 and CO2
Arachnoid Villus Cells
Carries out one-way bulk flow of CSF from subarachnoid space to venous sinuses via giant vacuoles
Circumventricular Organs
Blood-brain barrier is interrupted allowing the brain to respond to changes in the chemical milieu of the remainder of the body 1. Organum Vasculosum 2. Median Eminence 3. Neurohypophysis 4. Area Postrema - also known as the chemotactic trigger zone, involved in detecting circulating toxins that cause vomiting 5. Subcommissural Organ 6. Pineal 7.Subfornical Organ
Area postrema
the only paired circumventricular organ; located on the caudal wall of 4th ventricle in the medulla
Also known as chemotactic trigger zone --> detects circulating toxins that cause vomiting
Cytotoxic Edema
Cellular damage that can cause excessive intracellular fluid accumulation within the brain cells
Vasogenic Edema
Disruption of the blood-brain barrier resulting in the extravasation of fluids into the interstitial space
Headache mechanism
Caused by mechanical traction, inflammation, or irritation of the structures in the head that are innervted (blood vessels, meninges, scalp, skull)
Innervation supratentorial dura
Trigeminal (CN V)
Innervation dura of posterior fossa
CN X (to a lesser extent CN IX and first 3 cervical nerves)
Vascular Headache
not fully understood, but thought to involve inflammatory, autonomic, serotonergic, neuroendocrine and other associated symptoms (migraine or cluster headache)
Migraine
75% of patients have a positive family history, suggesting a genetic basis, symptoms may be provoked by certain foods, stress, eye strain, menstrual cycle, changes in sleep pattern. Usually unilateral; presence of aura
Symptoms of Migraine
Often preceded by an aura or warning symptoms, classically involving visual blurring, shimmering, scintillating distortions or fortification scotoma, pain is often throbbing and may be exacerbated by light (photophobia) sound (phonophobia) or sudden head movement. Nausea and vomiting may occur. 30 minutes - 24 hours
Fortification Scotoma
Characteristic region of visual loss bordered by zigzagging lines resembling the walls of a fort
Complicated Migraine
May be accompanied by a variety of transient focal neurologic deficits including sensory phenomena motor deficits visual loss brainstem findings in basilar migraine and impaired eye movements in ophthalmoplegic migraine
Treatment of Migraines
Acute attacks usually respond well to nonsteroidal anti-inflammatory drugs, anti-emetics, triptans (seretonin agonists, or resting in a quiet dark room)
Migraine Prevention
prophylaxis with beta-blockers, topriamate, valproate, calcium channel blockers, tricyclic antidepressants, NSAIDS
Cluster Headache
Less than 1/10th as common as migraine. 5x more common in males than in females. Lasts 30-90 minutes usually felt behind eyes. Usually accompanied by unilateral autonomic symptoms
Tension Headache
(aka tension-type headache) steady dull ache sometimes described as a bandlike sensation
Tx Tension Headache
muscle relaxation techniques, NSAIDS, other analgesics, tricyclic antidepressants
Sudden "explosive" onset of severe headache differential dx
subarachnoid hemorrhage
Headache accompanied by fever, stiff neck, sensitivity to light
possible infectous meningitis
Idiopathic Intracranial Hypertension
(aka Pseudotumor cerebri) condition of unknown cause characterized by headache and elevated intracranial pressure with no mass lesion. More common in adolescent females, treated with ACETAZOLAMIDE (or with shunting procedures)
Temporal Arteritis (Giant Cell Arteritis)
Important treatable cause of headaches, this disorder seen most commonly in elderly individuals, vasculitis affects the temporal arteries and other vessels, including those supplying the eye. Temporal artery is characteristically enlarged and firm.
Diagnosis of Temporal Arteritis
Diagnosis by erythrocyte sedimentation rate (ESR) and temporal artery biopsy
Effects of Intracranial Mass Lesion
1. Compression and destruction of adjacent regions of the brain causing neurological abnormalities
2. Mass located within cranial vault can raise the intracranial pressure causing certain characteristic symptoms and signs
3. Mass lesions can displace nervous system structures so severely that they are shifted from one compartment into another situation called herniation
Mass Effect
Distortion of normal brain geometry due to a mass lesion - can be as subtle as a mild flattening or effacement of sulci next to a lesion.
Midline Shift
results from mass effect caused by large masses which dramatically shift brain structures away from the side of the lesion, can compression ventricular system and obstruct CSF flow producing hydrocephalus.
Landmark the measures midline shift
pineal calcification
Elevated Intracranial Pressure
Severely elevated intracranial pressure can cause decreased cerebral blood flow and brain ischemia, cerebral blood flow depends on cerebral perfusion pressure.
Cerebral Perfusion Pressure
Mean arterial pressure minus the infusion pressure (CPP = MAP - ICP)
As intracranial pressure increases, cerebral perfusion pressure decreases. Autoregulation of cerebral vessel caliber can compensate for modest reductions in cerebral perfusion pressure leading to relatively stable cerebral blood flow however large increases in intracranial pressure can exceed the capacity of autoregulation leading to reduced cerebral blood flow and brain ischemia
Symptoms of Elevated Intracranial Pressure
-Headache (often worse in morning due to brain edema increasing overnight from effects of gravity)
-Altered mental status (especially irritability and depressed level of alertness and attention)
-Nausea and vomiting (typically suddenly and without much nausea known as projectile vomiting)
-Papilledema (elevation of optic disc)
-Visual Loss
-Diplopia
-Cushing's Triad (Hypertension, Bradycardia, Irregular respirations)
Cushing's Triad
Hypertension, Bradycardia, and irregular respirations
Normal Intracranial Pressure
In adults is less than 20 cm H2O or less than 15 mm Hg (torr)
Contraindication of Lumbar Puncture
Severely increased intracranial pressure (can precipitate herniation)
Tx Intracranial Pressure: Elevation of head of bed to 30 degrees,maintaining head straight
Immediate effect; promotes venous drainage
Tx Intracranial Pressure: Hemicraniectomy
Immediate effect; decompresses intracranial cavity (experimental)
Tx Intracranial Pressure: intubation and hyperventilation to PCO2 of 25-30mmHg
Onset = 30 seconds; causes cerebral vasoconstriction
Tx Intracranial Pressure: IV mannitol and furosemide
Onset = 5 minutes; promotes removal edema and other fluids from CNS while maintaining cerebral perfusion
Tx Intracranial Pressure: Ventricular drainage
Onset = minutes; removal of CSF decreases intracranial pressure
Tx Intracranial Pressure: barbiturate-induced coma
Only if all other measures fail; onset = 1 hour; causes cerebral vasoconstriction and reduced metabolic demands
Tx: Intracranial Pressure: Steroids
Onset = hours; reduces cerebral edema, possibly by strengthening blood-brain barrier; may also work by other mechanisms
Herniation
Occurs when mass effect is severe enough to push intracranial structures from one compartment into another.
3 Most Clinically important Herniation Syndromes?
1. Herniation through tentorial notch (transtentorial herniation)
2. Herniation centrally and downward (central herniation)
3. Herniation under the falx cerebri (Subfalcine herniation)
Transtentorial Herniation
Herniation of medial temporal lobe, especially the uncus (uncal herniation) inferiorly through the tentorial notch.
Clinical Triad Uncal Herniation
Heralded by clinical triad of "blown" pupil, hemiplegia, and coma.
Compression of Oculomotor (CN III) ipsilateral (85% of time) to the lesion produces first a dilated unresponsive pupil (blown pupil)
Compression of the cerebral peduncles can cause
hemiplagia (often contralateral to lesion)
Kernohan's Phenomenon
Sometimes in uncal herniation the midbrain is pushed all the way over until it is compressed by the opposite side of the tentorial notch, in these cases the contralateral corticospinal tract is compressed producing hemiplegia that is ipsilateral to the lesion.
Distortion of the midbrain reticular formation leads to...
decreased level of consciousness and ultimately, coma
Central herniation
central downard displacement of the brainstem
Causes central herniation
any lesion associated with elevated intracranial pressure
Mild central herniation
Traction of the abducens nerve --> lateral rectus palsy
Tonsillar herniation
herniation of the cerebellar tonsils downward through the foramen magnum --> associated with compression of the medulla and usually leads to respiratory arrest, blood pressure instability, and death
Subfalcine herniation
Herniation under the falx cerebri from one side of the cranium to another; can lead to infarcts of the anterior cerebral artery
Concussion
reversible impairment of neurologic function for a period of minutes to hours following a head injury; mechanism unknown
Clinical features concussion
loss of consciousness, headache, dizziness, nausea, vomiting; anterograde or retrograde amnesia
postconcussive syndrome
headaches, lethary, mental dullness lasting severeal months after accident
Diffuse axonal shear injury
causes widespread or patchy damage to the white matter and cranial nerves
Petechial hemorrhages
small spots of blood in the white matter
Types of intracranial hemorage
1. Epidural Hematoma (EDH)
2. Subdural Hematoma (SDH)
3. Subarachnoid hemorrhage (SAH)
4. Intracerebral or intraparenchymal hemorrage (ICH)
Location EDH
in the tight potential space between the dura and the skill
Causes EDH
Rupture of the middle meningeal artery due to fracture of the temporal bone by head trauma
Clinical features and radiological appearance EDH
Rapidly expanding hemorrhage under arterial pressure peels dura away from the inner surface of the skull; LENS shaped
Sx: initially, none; elevated intracranial pressure and ultimately, herniation
Location SDH
In the potential space between the dura and arachnoid
Usual causes of SDH
Rupture of the bridging veins
Radiological appearance SDH
crescent-shaped hematoma
Chronic SDH
often seen in elderly patients; blood collects over long period of time; headache, cognitive impairment, unsteady gait, focal seizures
Acute SDH
high impact velocity; areas in imaging are hyperdense and bright (acute blood) --> clot in 1-2 weeks (isodense); 3-4 weeks (hypodense)
continuous bleeding = mixed density
hematocrit effect
With mixed-density hematomas, the denser acute blood settles to the bottom
Location SAH
In the CSF-filled space between the arachnoid and the pia, which contains the major blood vessels of the brain
Radiological appearance SAH
Blood can be seen on CT to track down into the sulci following the contours of the pia (blood EVERYWHERE)
Nontraumatic (Spontaneous) SAH
presents as "the worst headache of my life"
causes: arterial aneurysm (or less commonly an AV malformation)
Risk factors intracranial aneurysm
atherosclerotic disease, congenital anomalies in cerebral blood vessels, polycystic kidney disease, connective tissue disorders (Marfan's)
Berry aneurysms
usually arise from Circle of Willis; typically have a neck and dome that can rupture
over 85% occur in the anterior circulation (carotid artery and its branches)
Most common locations: Berry aneurysms
AComm (30%), PComm (25%), MCA (20%), vertebrobasilar system (15%)
Are fusiform or saccular aneurysms less prone to rupture?
fusiform
Consequences of PComm aneurysm
Third nerve palsy
Risk factors aneurysm rupture
hypertension, smoking, alcohol, situations with elevation of BP
Type of scan to run for suspected hemorrhaging
CT scan WITHOUT contrast; both subarachnoid blood and contrast material appear white on the scan
Triple H Therapy
treatment of vasospasm following hemorrhage--> Induced Hypertension, hypervolemia, and hemodilution
Traumatic Subarachnoid Hemorrhage
caused by bleeding into the CSF from damaged blood vessels associated with cerebral contusions and other traumatic injuries; more common than spontaneous; severe headache
Location ICH
Within the brain parenchyma in the cerebral hemisphere, brainstem, cerebellum or spinal cord
Traumatic ICH
Contusions which are common at the temportal and frontal poles
Contusions occur on the side of the impact (coup injury) as well as on the side opposite the impact (contrecoup injury) because of rebound of the brain against the skull
Nontraumatic ICH Causes
hypertension, brain tumors, secondary hemorrhage after ischemic infarction, vascular malformations, blood coag abnormalities, infections, vessel fragility caused by deposition of amyloid protein in the blood vessel wall (amyloid angiopathy), vasculitis, mycotic (infectious) aneurysms in the setting of endocarditis
Hypertensive hemorrhage
most common cause of nontraumatic ICH
often involves small, penetrating blood vessels
uncertain pathogenesis, but may be related to chronic pathologic effects of hypertension on the small vessels (lenticulostriate arteries, including lipohyalinosis and microaneurysms of Charcot-Bouchard)
Most common locations of hypertensive hemorrage
Basal ganglia (usually the putamen)
thalamus
cerebellum
pons
Intraventricular extension
aka intraventricular hemorrhage; hemorrhages that involve the ventricles
Lobar hemorrhage
bleeding involves the occipital, parietal, temporal, or frontal lobe
Common cause of lobar hemorrhage
amyloid (congopilic) angiopathy
Vascular Malformations
1. AV malformations
2. Cavernomas
3. Capillary telangiectasias (capillary angiomas)
4. Developmental venous anomalies (venous angiomas, venous malformations)
Ateriovenous malformations (AVMs)
congential abnormalities in which there are abnormal direct connections between arteries and veins, often forming a tangle of abnormal blood vessels visible as flow voids on MRI scan, but best seen on conventional angiography
Tx AVM
neurosurgical removal, intravascular embolization, sterotactic radiosurgery
Cavernomas
abnormally dilated vascular cavities lines by only one layer of vascular endothelium
not visible on conventional angiography
Have a characteristic MRI appearance (central 1-2cm core of increased signal on T1 or T2, surrounded by a dark rim on T2-weighted sequences because of hemosiderin)
Capillary telangiectasia
small regions of abnormally dilated capillaries; rarely give rise to intracranial hemorrhage
Developmental venous anomalies
dilated veins usually visible on MRI scans as a single flow void extending to the brain surface
Hemotympanum
hemorrage in the inner ear
Hemorrage in subcutaneous tissue
results in Battle's sign or "racoon eyes"
Subgaleal hemorrhage
hemorrage in the loose space between the external periosteum and galea aponeurotica; can produce a "goose egg"
cephalohematoma
bleeding during delvery of newborns that occurs between the skull and external periosteum (pericranium)
Causes of hydrocephalus(3)
1) excess CSF production 2) Obstriction in ventricles or subarachnoid space 3) decrease in reabsorption via arachnoid granulations
Excess CSF Production
rare, seen in choroid plexus papilloma
Obstruction of CSF flow
common cause, especially at narrow points-foramen of monro, cerebral aqueduct, 4th ventricle
Decreased CSF Resorption
difficult to distinguish from obstruction and often has similar causes.
Communication Hydrocephalus
impaired CSF resorption in arachnoid agranulation, obstricution of flow in the subarachnoid space, or (rarely) by excess CSF production
Noncommunication hydrocephalus
obstruction fo flow w/in the ventricular system
Symptoms of hydrocephalus
Headache, nausea, vomiting, coagnitive impairment, decreased level of consciousness, papilledema, decreased vision, 6th N palsies(incomplete or slow abduction of eye), magnetic gait[feet barely leave the floor](assc with frontal lobe) and incontinence
Parinaud's Syndrome
dilation of the suprapineal recess of the posterior 3rd ventricle pushing downward onto the collicular plate. Causes limited upward gaze.
"setting sun" sign
bilatreal deviaton of the eyes downward and inward. Most often in children with acute hydrocephalus
Ventriculoperitoneal shunt
shunt tubing from lateral ventricle tunneled under the skin into the peritoneal cavity of the abdomen. Valve prevents reverse fluid direction.
Endoscopic Neurosurgery
cannula introduced into the cranium through small incision and passing instruments through it
Normal Pressure Hydrocephalus
condidtion usually in elderly, chronically dilated ventricles. Present with clinical triad of gait difficulties, urinary incontinence, and mental decline. Thought to be form of communicating hydrocephalus with impaired CSF resorption at the arachnoid villi.
Hydrocephalus Ex Vacuo
Refers to excess CSF in a regionwhere brain tissue was lost as a result of stroke, surgery, atrophy, trauma or other insult.
2 broad categories of brain tumors
Primary CNS tumors and Metastatic Tumors
Primary CNS tumors
arose from abnormal proliferation of cells originating in the nervous system
Metastatic tumors
arise from neoplasms originating elsewhere in the body that spread to the brain
Most common brain tumors
gliomas and meningiomas
Supratentorial tumors are more common in
adults
Infratentorial tumors are more common in
children
Most common brain tumors in children
astrocytoma and medulloblastoma, followed by ependymoma
Various symptoms of brain tumors
headache and other signs of increased intracranial pressure, seizure and focal symptoms
Tumors that are more commonly associated with seizures
low-grade gliomas and meningiomas
Types of gliomas
Glioblastoma multiforme
Astrocytoma Grades I and II
Asytrocytoma Grade III
Oligodendriglioma
Ependymoma
Other
Meningiomas
arise from the arachnoid villus cells and occur, in order of decreasing frequency, over the lateral convexities, in the falx, and along the basal regions of the cranium
In female pts, there may be an association between meningiomas and breast cancer
Pituitary adenomas
Can cause endocrine disturbances or compress the optic chiasm
Tx pituitary adenoma
dopaminergic agonists or transsphenoidal resection
Prolactinomas
most common type of pituitary adenoma
Most common schwannoma location
CN VIII
Lymphoma
increased incidence attributable to increase in HIV
Arises from B cells
controlled by chemotherapy and radiation therapy
Pineal region tumor
Relatively uncommon
Includes pinealomas, germinomas, and rarely, teratomas or gliomas
Tumors in this region can obstruct cerebral aqueduct or compress the dorsal midbrain, causing Parinaud's syndrome
Most common cancers that spread to brain
lung, breast, melanoma
Cerebellar astrocytoma
Grade I astrocytoma; often cured by surgical ressection
Common age range medulloblastoma
before age 10
Common age range cerebellar astrocytoma
between 2 and 20
Paraneoplastic syndrome
Relatively rare neurologic disorder caused by remote effects of cancer in the body, leading to an abnormal autoimmune response
Examples: limbic or brainstem encephalitis, cerebellar Purkinje cell loss, spinal cord anterior horn cell loss, neuropathy, impaired neuromuscular junction (Lambert-Eaton syndrome), and opsoclonus myoclonus (characterized by irregular jerking movements of the eyes and limbs)
Infectious Meningitis
infection of the CSF in the subarachnoid space
Causes infectious meningitis
bacteria, viruses, fungi, or parasites
Sx infectious meningitis
Headache, lethargy, photophobia, phonophobia
Dx of meningitis
CT followed by lumbar puncture
CSF characteristics of Bacterial meningitis
CSF = high white blood cell count with polymorphonuclear predominance
High protein
Low glucose
Most common pathogens in bacterial meningitis
depends on age
Most common tx bacterial meningitis
depends on age
Most common pathogen bacterial meningitis for children <3 months
E Coli, Group B, D Streptococcus, Listeria
Most common pathogen bacterial meningitis 1 month-7 years
Haemophilus influenzae, Neisseria meningitidis, streptococcus pneumoniae
Most common pathogen bacterial meningitis ages 7 years-adult
Listeria, Neisseria meningitidis, Streptococcus pneumoniae
Most common tx bacterial meningitis ages 0-3 months
Ampicillin + ceftriaxone
Most common tx bacterial meningitis ages 3 months - 7 years
Ceftriaxone
Most common tx bacterial meningitis ages 7 years - adult
Ampicillin + ceftriaxone
Complications of bacterial meningitis
seizures, cranial neuropathies, cerebral edema, hydrocephalus, herniation, cerebral infarcts, and death
What do you do with children following recovery of bacterial meningitis?
screen for hearing loss
Brain abcess
bacterial infection of the nervous system; presents as an expanding intracranial mass, much like a brain tumor, but with a much more rapid course
presentation brain abcess
headache, lethargy, fever (60% of cases), nuchal rigidity, nausea, vomiting, seizures, focial signs
Common infecting organisms: brain abscess
streptococci, Bacteriodes, enterobacteriaeae, Staphylococcus aureus, toxoplasma gondii, Nocardia
Tx patients small brain abscess (<2.5 cm)
antibiotics and observation
Tx pts with large brain abscess (>2.5cm)
stereotactic needle aspiration or surgical removal + antibiotics
CSF of Viral Meningitis
increased WBC (10-300); increased protein (50-100); normal glucose (exception = herpes, mumps, lymphocytic choriomeningitis virus)
CSF of Herpes meningoencephalitis
0-500 lymphocytes (normal = <5-10); increased protein (5-100); Normal or reduced glucose; RBCs or xanthochromia may be present
CSF of tuberculous menigitis or cryptococal meningitis
increased lymphocytes (10-200); increased protein (100-200); reduced glucose (<50)
Most common location epidural abscess
spinal canal
Common presentation epidural abscess
back pain, fever, elevated peripheral white blood cell count, headache, signs of nerve root or spinal cord compression
Ex epidural abscess
surgical drainage and antibiotics (nafcillin and ceftriaxone)
Pathogen epidural abscess
Staphylococcus aureus, streptococci, Gram-negative bacilli, and aneorobes
Sudbdural empyema
collection of pus in the subdural space, usually resulting from direct extension from an infection of the nasal sinuses or inner ear
Tx subdural empeyma
ceftriaxone + metronidazole
Pott's disease
tuberculous involvement of the epidural space
Tx tuberculous meningitis
combination of isonizid, rifampicin, ethambutol, and pyrazinamide
Lymphocyte-Predominant Meningitis
"Aseptic meningitis"
most commonly viral in origin
2 most important spirochetal infections of the nervous system
neurosyphilis and Lyme disease
Syphilis pathogen
Treponema pallidum
Primary syphillis
painless skin lesions called chancres appear at the site of infection about 1 month after exposure
Secondary syphilis
more diffuse skin lesions appear ~ 6 months (palms and soles)
Tertiary syphilis
neurologic manifestations
meningovascular syphilis
chronic meningeal involvement causes arteritis, typically involving medium sized vessels, that results in diffuse white matter infarcts
What occurs if meningovascular syphilis goes untreated?
general paresis-- accumulation of lesions causes dementia, behavioral changes, delusions of grandeur, psychosis, and diffuse UMN-type weakness
Tabes dorsalis
syphilitic myelopathy with degeneration of spinal cord dorsal roots; sensory loss and high stepping gait pattern and incontinence; Argyll Robertson pupils and optic atrophy
Dx neurosyphilis
blood tests for treponems (FTA-ABS or MHA-TP) + CSF w/ lymphocyte-predominant meningitis
Tx neurosyphilis
IV penicillin G
Lyme disease pathogen
Borrelia burgdorferi carried by Ixodes species of deer tick
Sx Lyme Disease
erythema chronicum migrans (rash); some cases show neurologic manifestations (lymphocyte-predominant meningitis, mild meningoencephalitis, emotional changes, crainial neuropathies (most commonly CN VIII)); arthritis and cardiac conduction abnormalities
Tx Lyme Disease
IV ceftriaxone
Causes viral meningitis
enterocviruses such as echovirus, coxsackievirus, mumps virus
Viral encephalitis
viral infections that involve the brain parenchyma
Most common cause viral encephalitis
herpes simplex Type I
Herpes Simplex encephalitis
causes necrosis of unilateral or b/l temporal and frontal sutures; progresses within days to coma and death
Tx Herpes Simplex encephalitis
Acyclovir
Subacute sclerosing panencephalitis
A delayed, slowly progressive fatal encephalitis often associated with measles
Herpes Zoster
shingles; infection caused by the same virus as chickenpox
primary sx = painful rash conforming to nerve root distributions
HTVL-1 virus
causes chronic type of spinal cord disease called HTVL-1 associated myelopathy, or tropical spastic paraparesis
Causes of transverse myelitis
enteroviruses (coxsakie and poliomyelitis), varicella-zoster virus, HIV
less commonly, Epstein-Barr virus, cytomegalovirus, herpes simplex, rabies, Japanese B virus
HIV-associated neurocognitive disorder (HAND)
common neurologic manifstation of HIV, with increasd frequency late in the course of the illness; Tx with antiviral agents (highly active antiretrovial therapy, or HAART) can cause improvement in AIDS related dementia
Common viral infections in pts with HIV
encephalitis, herpes simplex virus, varicella-zoster virus, or cytomegalovirus
Progressive multifocal leukoencephalopathy (PML)
Disorder that can occur in patients w/ AIDS or immunodeficiency status; caused by papvavirus called the JC virus and results in gradual demyelination of the brain (death within 3-6 months)
Important bacterial infections in pts with AIDS
tuberculous meningitis and neurosyphilis
Cryptococcal meningitis
common fungal infection in AIDS pts; should be suspected in all HIV-positive pts with chronic headache; organism can be identified by India ink stain
Tx cyrptococal meningitis
IV amphotercin B followed by oral fluxonazole
Exposure to toxoplasma
undercooked meat or cysts in cat feces; initial exposure is usually asymptomatic
Toxoplasma and AIDS pts
infection becomes reactivated and spreads to the CNS, forming brain abscesses visible on MRI scans as ring-enhancing lesions
Most common cause of intracranial mass lesions in pts with HIV
toxoplasmosis (second = primary nervous system lymphoma)
Tx toxoplasmosis
pyrimethamine and sulfadiazine
Primary nervous system lymphoma
B cell lymphoma that can appear radiologically similar to toxoplasmosis
Tx primary nervous system lymphoma
steroids and radiation therapy
Pathogen African sleeping sickness
Trypanosoma brucei
Cysticerosis
caused by ingestion of the eggs of the pork tapework Taenua solium; organism migrates through the bloodstream to the whole body forming multiple cysts in the muscles, eyes, and CNS
Sx Cysticerosis
Seizures, headache, nausea, vomiting, lymphocytic meningitis, focal deficits, hydrocephalus
Tx Cysticerosis
albendazole
Mucormycosis
Potentially fatal fungal infection that occurs mainly in diabetics in the rhinocerebral form and involves the orbital apex
Rhinocerebral mucormycosis
causes opthalmoplegia, facial numbness, visual loss, facial weakness; typical violet coloration of the tips of the eyelids
Tx mucormycosis
Amphotercin C; steroids should be avoided
Prion related illnesses
infectious agents that are protein-based contains no DNA or RNA
Pathologically diffuse degeneration of the brain and spinal cord occurs, with multiple vaculoes results in a spongiform appearance
Examples prion related illness
Creutzfeldt-Jakob disease, Gerstmann-Strauessler-Scheinker disease, kuru, and fatal familial insomnia
Creutzfeldt-Jakob Disease
presents with rapidly progressive dementia, an exaggerated startle response, myoclonus, visual distortions or hallucinations, and ataxia; MRI shows periodic sharp wave complexes and CSF shows increased 14-3-3 protein; no treatment available; may have been caused by ingestion of cattle infected with bovine spongiform encephalopathy
What should you do before performing a lumbar puncture?
Perform head CT to avoid risk of herniation
Normal CSF pressure in adults
less than 20 cm H2O
Ending spinal cord in adults
L1/L2
Loation of Lumbar puncture
between L4/L5; posterior iliac crest = landmark
Indication of RBCs are present in CSF
hemorrhagic encephalitis
Traumatic tap
damage to blood vessels caused by spinal needle at the time of the lumbar puncture
Presence of xanthochromic supernatant in CSF
indication that the hemorrhage is older
Pterion
region over the temporal where the frontal, parietal, temporal and sphenoid bones meet
Pterional craniotomy
provides access to the inferiortemporal lobes; used for surgey on anterior circulation and basilar tip aneurysms, the cavernous sinus, and suprasellar tumors
Temporal craniotomy
a more lateral approach; used for operating on the temporal lobe to resect seizure foci and for decompression of most intracranial hematomas
Frontal craniotomy
used for frontal lobe lesions such as tumors
Suboccipital craniotomy
access to posterior fossa stuctures such as cerebellopontine angle, vertebral artery, brainstem, and lower cranial nerves
transspenoidal approach
pituitary region reached through nasal passages
sterotactic procedures
an instrument is introduced through a small burr hole and directed to a specific target within the deep brain
Sx: Lt hemiparesis and Lt Babinski sign, Visual and tactile extinction(form of hemineglect) on the Lt, Rt sided headaches, Generalized fatigue All gradually worsening following a car crash 3 mos ago
Right hemisphere cortical and or subcortical lesion affecting corticospinal and attentional pathways. Gradual worsening suggests chronic subdural hematoma(crescent shape on MRI) (2-3 weeks for hematoma to become hyp0dense, acute=hyperdense) midline shift seen with mild subfalcine herniation. Treated by surgical evacuation.
Sx: Unresponsiveness except to painful stimuli, Abscent Rt corneal reflex, and no Rt arm or leg movement in response to pain, with plantar response absent on the Rt and upgoing on the Lt. Drunk at the bottom of stairs
Alcohol can skew neuro exams but it should get better with time, if not imaging done immediately. Most likely epidural hematoma, acute subdural hematoma, cerebral contusion or cerebral edema. Coup Contrecoup-blow to one side of the head is accompanied by decelration ninjury on the opposite side of the brain as it bangs against the inner surface of the skull; frontal and temporal poles especially susceptible to contusion. Midline shift seen at the level of the pineal calcification(>10mm shift is usually assc with profound coma.) Also had early Lt uncal transtentorial herniation. basal cisterns at near complete effacement. Lt lat ventricle and culci completely obliterated. Lt hemispheres swollen and somewhat hypodense, consistent with diffuse cerebral edema.