KNOW all the possible complications of STROKES from the following branches in the objectives, along with the superior & inferior division of the MCA, and the circle of willis in it’s entirety. Know the lobes & all the information they could lose, especially all the lobes involved with vision, voluntary eye movements, etc. Also, aphasia & all the different types and which ones are in which lobes and infarction present how, expression, conductive, word salad, you get the idea. Also, know what to do & what not to do w/ a patient with an acute head injury, in a stepwise fashion, who may be unresponsive. Order does matter and was specific. Know the thyroid and its implications to neurology in detail. This stuff was tested and not really covered well in the objectives, but remember this is only a few peoples opinion. Julie Scott’s notes are pretty well used by most but with a disk you can cut, delete, add & edit, not to mention print for free in the
LRC! Good luck ! Kim Northup, 2002
Unit One Cerebrovascular Disease
3 Categories of stroke
ischemic (usually thrombotic > embolic)
hemorrhage (usually embolotic at bifurcations of large arteries like MCA)
lacunar or deep infarcts in the Internal capsule, or Grey matter i.e. potential seizure foci
Risk Factors:
Natural:
-age, gender, &race
Preventable:
HTN, hyperlipidemia, diabetes, valve abnormalities smoking, ETOH
Artery distribution:
ACA CL weakness or numbness Legs > arm, MIXED motor& sensory
Loss of decision making capacity (abulia), Urinary Incontinence
CL weakness or numbness Arms & face, CL hemianopsia, CL gaze
Palsy (Eyes Look to the Lesion), Aphasia for dominant and neglect if
Nondominant, MIXED motor and sensory interrupted visual radiation, Wernicke’s aphasia
MCA
Superior branch
Inferior branch of MCA
PCA
PCA bilaterally
PCA branches
Verterbrobasilar
AICA
PICA branch of vertebral
Lacunar Infarcts of deep
Grey cortical matter
CL hemianopsia, pure sensory or pure motor syndrome
Cortical blindness, prosoagnosia
CL hemibalism if the subthalamic nucleus is involved
Ataxia, vertigo, diplopia, dsyarthria, dysphagia, ipilateral CN, with
Weakness and numbness in extremeties (crossed finding)
Pons, gaze palsy, ipsilateral facial weakness, deafness possibly
Wallenberg’s syndrome of CL loss of P & T ipsilateral CN findings,
Ipsilateral Horners, ataxia, nystagmus, hoarseness, dysphagia
Basal ganglia, Pons, cerbellum, and anterior limb of IC
CL pure motor or pure sensory hemiparesis Ipsilateral ataxia
Anterior Spinal Artery
1 st branch of the vertebral
Carotid dissection
CL UMN hemiplegia near C5 w/ infarct of spinal cord, CN XII nucleus
Basal brainstem infarct usually due to trauma & can present with a Horner’s from SNS fibers
CN III, VI, VIII , CL hemiparesis
Thrombotic occulsions are almost always atherosclerotic and occur at IC & carotid bifurcation or in the vertebrobasilar system depending upon the normal functioning of the Circle of Willis.
Asymptomatic Carotid Bruit - between 30-70% occulded usually

TIA - stroke w/neurological signs resolving in < 24 hrs ; usually in 30 min, and recurrent TIAs could be due to cardiac or thromobosis or embolism in the cerebral circulation
Lacunar Infarct - occlusion of small penetrating branches from hyalinosis due to HTN, DM, and atherosclerosis
Hemorrhagic infarct- vessel imcompetence leading to destructive or compressive bleeding that can lead to ischemic infarct or edema, presents w/ a severe HA and LOC
Carotid Endarterectomy- surgical removal of thrombus from stenotic carotid arteries w/ stenosis > 70% used for unstable TIA’s w/ major risk of stroke, not done in vertebrobasilar system
Spontaneous Hemmorhage -
ruptured cerebral artery aneurysm
AVM’s men > women 2:1, ages 20-40 yo
Berry aneurysms 50-60 yo ass’d w/ APKD
Cocaine or Amphetamine use
Trauma
Clincial findings of hemmorhage
increased ICP, finding is papilledema
“worst Headache of my life!!”
LOC, vomiting, neck stiffness, confusion, stupor, coma
Increased BP, T
Work up
CT/MRI
LP (increased opening pressure, pleocytosis w/ xanthrochromia post hemorrhage)
ECG short PR interval w/tall inverted T waves
Arteriography
Nimodipine (decreases cerebral vasospasm but can cause bradycardia)
Surgical clipping or wrapping/ En Bloc resection of AVM if accessible
Bedrest w/ head up, manage pain w/ analgesics NOT Aspirin
-
Watch IV fluids to make sure they aren’t increasing ICP
Cerebral Infarcts
1-4 hrs no changes possibly detected by MRI
detectable at 12 hrs w/ softening of the gray matter seen on MRI swelling, dead red neurons + PMN more apparent swelling 48-72 hrs ** may cause herniation WATCH DAY 3 MRI/CT visible most likely
2-6 days macrophages are the predominate response w/ maximal edema achieved
signs of edema are altered conciousness, projectile vomiting, pupillary changes
1-3 wks reactive astrocytes, small BV perfusion, beginning of liquifaction w/ macrophages
months to years resolution via liquifaction, cystic degeneration or cavitation w/ astrocytes around the edge, or glial formation
Work up for Ischemic Stroke
ECG to look for cardiac source MI or A- fib
CT or MRI to look for infarct or hemorrhage and R/O lesions or tumors
LP to r/o SAH
Carotid Doppler Ultrasound study
Echocardiogram for embolic source
EEG to distinguish seizure vs. TIA or Lacunar vs. cortical
MR Angiography
Classic Carotid Emboli= ipsilateral blindness (amarousis fugax approx 10 mins), CL hemiparesis
Classic Vertebrobasilar= drop attacks, bilateral blindness, confusion, vertigo
Watershed infarcts secondary to hypoperfusion near MCA-ACA border; with reperfusion can be bilateral and/or hemorrhagic

Hemorrhage can be intraparenchymal, subarachnoid, or mixed usually due to vascular damage
VS. Hemorrhagic infarct- a white infarct that has been reperfused, looks like petechial hemorrhages
Pathogenesis of Atherosclerosis
development of focal area of endothelial damage with increased permeability to lipid insudation, monocyte and platelet adherence
intimal aggregate of monocytes and macrophages
chemotactic and growth factors causing smooth muscle (intimal) proliferation
macrophages and smooth muscle cells engulf lipids forming “foam cells”
surface plaque can ulcerate, break off and lead to embolus and thrombotic infarction
DDx of Intercranial Hemorhages
Hypertensive hemorhages - intraparenchymal bleeds in regions served by perforator arteries caused by rupture of charcot-bouchard microaneurysm most frequently in basal ganglia, pons, cerebellum, 40% mortality, with resolution there may be some restoration of function
Gross Pathology
expansion of affected area
flattening of the gyri
herniation, midbrain displacement
ventricular distortion
Berry Aneurysms- bleeding into subarachnoid space occurs at the bifurcation of cerebral arteries or at sites of media weakness, rupture can be ass’d w/ acute increased ICP, common in APKD, fibromuscular dysplasia, AVM, but MOST are sporadic.
SX: sudden severe occipital HA, rapid LOC w/ 50% of patients dying
Other complications: infarction, hydrocephalus, herniation, brainstem hemorrhage, arterial vasospasm
AVM- 1% of intercranial tumors can rupture and bleed into grey matter of brain (setting up a seizure foci) or subarachnoid space, tortuous tangled vessels of various sizes, 90% are w/in the cerebral hemispheres, most common bleeds between the ages of 10-30 Males 2: 1 females
SX: Intercerebral hemorrhage W/ seizures
Supratentorial Hemorrhages- lead to progressive hemiplegia
Posterior Fossa/ Cerebellar Hematomas- lead to intractable vomiting, increased ICP, herniation, & coma
Epidural Hematoma - trauma, middle menigeal artery, lense shaped on CT that does not cross midline
Subdural Hematoma - in young and elderly, tearing of the bridging veins, cresent shape and can cross cranial sutures, shifting midline structures
Unit Two
CT scan Indicated in a stroke > 48 hrs or early to R/O acute bleed, tumor, trauma, dementia, cerebral hemorrhage
detection of structural abnormalities
speedy
good for evaluating progressive neurological disease or focal deficits due to strxl lesion
contrast improves detection of tumors & abscesses, AVM, chronic subdural hematomas
MRI Indicated in early stroke (w/1 st day), hematoma, tumor, trauma (parenchymal pathology), dementia,
MS or demyelinating diseases, and infections
better contrast between gray and white matter
better visualization of the posterior fossa and spinal cord

better detection of MS plaques or seizure foci
gadolinium enhancement (contrast) can separate small tumors vs. edema, identify leptomeningio disease, and integrity of the BBB
Superior to CT for MS, early stroke, tumors at vertex, posterior fossa, and acoustic neuromas
Arteriography
for visualizing intercranial circulation
catherization into femoral or brachial a. to a major cervical vessel w/ contrast to visualize cerebral vessels
risks 1% morbidity/mortality and considerable radiation exposure
MR Angiography (MRA)
for visualizing carotids, and proximal areas of intercranial circulation where flow is fast
screening tests for stenosis, plaques, & venous sinus occlusion
- if more than 70% consider carotid endarterectomy
EEG
non invasive recording of electrical activity of brain w/leads placed on scalp
for evaluation of epilepsy, abnl rhythmic electrocerebral activity of abrupt onset and termination a negative EEG can not R/O epilepsy not matter how many days it is followed
for classification of seizures disorder to determine type for proper anticonvulsant therapy
for assessment and prognosis of seizures & management of status epilepticus
detection of structural brain lesions (foci)
diagnosis of neurological diseases, i.e. HSV encephalitis repetitive slow wave complexes & CJK/SSPE w/ presence of periodic complexes
evaluation of alterations of conscisouness, details of the level of coma
Evoked Potentials
potentials evoked by non invasive stimulation of specific afferent pathways to monitor functional activity of the pathway
common used in detection of MS lesions and monitoring functional status, spinocerebellar degeneration, familial spastic paraplegia, Vit E or Vit B12 def’y, assessment following CNS trauma or hypoxia, intraoperative monitoring, evaluation of auditory and visual
Types:
Visual w/ checkboard pattern stimulation recording potential from mid occipital region the clinical importance is the P100 response.
Auditory – monoaural stimulation w/ repetitive clicks elicites BS evoked potential recorded at the vertex of the scalp, senses potential in the first 10 ms, check for latency or increased intervals
Somatosensory - stimulation of peripheral nerves recorded at spine or scalp
EMG
assesses regional muscle activity via an electrode placed in muscle in passive and active states muscle activity at rest (passive state)
relaxed muscle, normally no spontaneous activity except at NMJ
fibrillation potentials = + sharp waves, deinnervated muscle seen in myopathic disease such as inflammatory myositis and poliomyositis, not seen on PEX
fasiculation potential= characteristic of neuropathic disease, especially ALS
myotonic discharge=myotonic dystrophy, congenital myotonia, and occasionally polio muscle in active state
myopathic disease= short, small duration, polyphasic motor units in affected (proximal) muscles
neuropathic disease= loss of motor units w/ decreased # of activated fiber with and increased rate of firing (in distal muscles) secondary myopathies common w/ statins & steroidal therapy
Poliomyositis is always Asymmetrical
Dermatomyosistis in kids is usually rheumatological & in adults it is probably a paraneoplastic syndrome

Nerve Conduction Studies
Motor Nerve conduction studies & Sensory nerve conduction studies
to comfirm the presence & extent of peripheral nerve damage
Carpal tunnel syndrome Dx’d with EMG/NC studies- sensory and motor velocities slowed at rest w/ possible signs of chronic, partial denervation of the median suppplied muscles of the hand
Lumbar Puncture
indicated for diagnosis of meningitis or other infective or inflammatory disorder such as SAH, hepatic encephalopathy, Guillan Barre, psuedotumor cerebri, & MS
assessment of treatment response
administeration of intrathecal meds or contrast
to reduce ICP pressure (rarely done)
contraindications : suspected intracranial mass lesion, local infection, coagulopathy, suspected spinal cord mass lesion, & a infarct w/ hydrocephalus
procedure= position pt in lateral decubitus position w/ maximal back flexion, site is between L3-L4 or
L4-L5 approximated by pt’s iliac crest, sterilized procedure w/ local anesthesia, bevel up, pop through tegmental flavum, enter subarachnoid space, measure opening pressure w/ stop cock. Pt may get post
LP HA.
Clinical uses of Biopsies
Brain-
primary tumors, metastatic tumors, HSV encephalitis, abscesses, CJD
Muscle
to distinguish neurogenic from myogenic causes: myositis, polio, DMD, BMD, myopathies, & mitochondrial d/o
Nerve
for metabolic storage diseases (Fabry’s, Tangier’s), infection (leprosy), inflammatory changes
(vasculitis) or neoplastic involvement
Artery biopsy
- Temporal artery for Giant cell arteritis
Unit 3 Disorders of Consciousness
Seizures excessive, oversynchronized discharges of cerebral neurons
Epilepsy- group of disorders characterized by recurrent seizures, episodic loss of consciousness, affecting
0.3% of population at one time in life. Possible etiologies include hereditary, perinatal injury, infection, post infarction stroke, and neoplasms (mass effect).
Benign Febrile Convulsions 2-4% of children between 3 mo – 5yrs, on the 1 st day of a non CNS febrile illness, lasts < 15 mins, non focal 2/3 have one seizure w/ < 10% having more than 3. Seizures occuring early in illness or w/ a family hx of seizures have a 90% risk of a recurrence w/in 2 years of the first seizure.
Generalized Seizures - (i.e. involving both hemispheres) & including absence seizure
primary generalized are usually in people < 20 and do not have an associated aura
tonic clonic- loss of consciouness, usually w/ a symptomatic aura or warning
tonic phase is unconsciousness w/ 10 Hz or faster waves, tonic contraction of limbs 10-30 sec, extension of limbs, arching of body, crying, cyanosis, contraction of muscles of massication (toungue biting)
clonic phase is alternating contraction /relaxation of muscle for 30-60 sec w/ slow waves & w/ return of ventilatory effort and clearing of cyanosis, frothy saliva, possible muscle flaccidity and incontinence.
Recovery or post ictal phase, can have confusion and HA, > 30 mins at times, positive Babinski at times, Todd’s paralysis (transient unilateral weakness suggesting focal brain lesion)

Absence Seizures-
genetic, always begin in childhood and usually end by age 20
brief LOC w/ loss of postural tone
subtle motor manifestations= eye blinking or head turning “automatisms”
no post ictal phase, full orientation
inducible by hyperventilation
3Hz/sec spike wave during seizure usually < 30 sec
Partial Epilepsy (i.e. focal)
Simple Partial
begins w/ motor, sensory, or autonomic pheonomenon or aura (i.e. pallor, flushing, sweating, pupil dilation, piloerection, vomiting, and incontinence)
psychiatric symptoms, dysphasia, distorted memory, affect disturbance, cognitive defecits, labored thought processes, & hallucinations w/o LOC
Complex Partial
temporal lobe or psychomotor episodes of impaired conscionnesss BUT NOT LOC
arises mostly from medial temporal or medial frontal ; possible HC formation
symptoms epigastric sensations, fear, déjà vu, olfactory hallucinations, before impaired consciousnesss
usually < 30 min w/ characteristic coordinated motor activities “automatisim” orobuccolingual movements, pupillary dilation or salivation.
Secondary generalization may occur if motor area is involved it will be a tonic-clonic
Systemic Diseases that predispose to seizures**know these
metabolic= hypoglycemia, hyponatremia, hypocalcemia
HTN, hepatic encephalopathy, uremia, porphyia
Drug overdose/withdrawal
Eclampsia/hyperthermia
Syncope
LOC due to decreased blood flow to brain, light headedness, dimming of vision, usually <15 sec w/ no post ictal confusion
Causes cardiac abnormalities; orthostatic hypotension, vasovagal reflex, cerebrovascular syncope
EEG
useful confirmatory test to distinguish seizure from other causes of LOC, can NOT exclude seizures
Epilepsy EEG findings
abnormal spikes, polyspike discharge, and spike wave complexes
Absence seizures
3Hz spike and wave activity, bilaterally symmetric and synchronous
Other Brain Disease detectable by EEG
structural brain lesions
evaluation of altered conscousness
herpes encephalitis- repetitive slow wave complexes
CJD/SSPE- periodic complexes
MRI/CT is indicated in all partial or focal seizure patients
Status Epilepticus
Seizures that fail to cease and recur w/o full consciousness being restored in between
THIS IS A MEDICAL EMERGENCY.. and can cause permanent brain damage
Most common cause is seizure drug N/C or withdrawal & alcohol WD, metabolic, infarcts, tumor
RX: ABC’s, IV Diazepam 10 mg/ 2 minutes, Phenytoin, Phenobarbital
Labs: CBC, metabolic panel, tox screen, ESR, UA
IV 50ml of 50% dextrose + thiamine

ABG & LP **know order
Primary Seizures vs Secondary Seizures
Phenytoin (Na Blocker) used in partial and GTC
Carbamazepine (Na B) used in partial and GTC
Phenobarbital (GABA) used in GTC
Valproic acid (Na B) used in GTC & absence & M
Ethosuximide (Ca+ B) used in absence ataxia , nystagmus , somulence ataxia, naseau, diplopia ataxia, somolence, memory problems ataxia, drowsiness, tremor nausea, anorexia @ onset
Coma
no purposeful response to the environment, unable to arouse, eyes typically closed, no speaking, may or may not withdraw to painful stimuli
caused by lesion above the midpons of the brainstem or w/ bilateral hemispheric involvement
Supratentorial causes
mass lesion
subdural hematoma (more common in elderly w/ atrophic brains and increased sheer force on cortical bridging veins with falling)
SX’s HA, alteration of consciousness, CL hemiparesis, ipsilateral pupillary dilation
RX: surgical evacuation
DX: CT shows crescent shaped hemorrhage that can cranial suture lines, & show midline shift of ventricles
epidural hematoma (more common in head traumas ass’d w/ lateral skull fracture tearing of the middle meningeal a. tear)
SX: Fine one minute, obtunded the next
RX: Medical emergency
DX: CT w/ lentiform (lens) shaped hemorrhage w/o crossing the suture lines
Subtentorial causes
basilar artery thrombosis or occlusion
RX: anti coagulation
pontine hemorrhage
Hypertensive patients w/ symptoms such as ocular bobbing, pinpoint pupils, w/loss of horizontal gaze
cerebellar hemorrhage or infarct
posterior fossa subdural or epidural hematomas
Hypoglycemia - in insulin overdose, alcoholism, insulinoma, or large retroperitoneal neoplasms, liver disease
condition must be treated w/ 50% dextrose w/in 60-90 minutes to prevent further damage
Global Cerebral Ischemiapost cardiac arrest
Drug Intoxication
Hepatic Encephalopathy
Examination /Treatment of a Comatose Patient
Coma Cocktail- 25 g Dextrose (corrects hypoglycemia), 100 mg thiamine (Rx Wernicke’s), 0.4-1.2 mg
Naloxone (Rx for opiod OD)
HX:
sudden onset= vascular (stroke or hemorrhage)
rapid progression from hemispheric Sx to coma = intracerebral hemorrhage
protracted course to coma= tumor, abscess, chronic subdural bleed
proceeded by confusional state= metabolic

PEX:
signs of basilar skull fracture: raccoon eyes, Battles sign, hemotympaneum, CSF rhinorrhea/otorrhea
decreased in basal body temperature w/ alcoholic Wernicke’s, sedative OD, or hepatic encephalopathy
increased in basal body temperature w/ heat stroke or status epilepticus
Pupil
nl is 3-4 mm
thalamic= smaller but reactive
CN III compression, anticholinergic OD, transtentorial herniation of medial temporal lobe=fixed dilated > 7mm non reactive
Brainstem at the midbrain level= Fixed mid sized pupils =5 mm
Opoid OD, focal pontine, Organophosphates, Neurosyphillis= Pinpoint 1- 1.5 mm
Midbrain structural lesion, CN III =Anisoconia, asymmetric pupils
Oculocephalic reflex “doll head” & Oculovestibular reflex (caloric) normal movement’s with intact brainstem fxn
Normal movements COWS ( cold opposite warm same)
Abnormal movements downward deviation w/ cold water= sedative OD
NO OVR = structural lesion at Pons
ABNL OVR = CNIII or midbrain lesion
Motor responses to Pain
Decorticate response- subcortical lesion involves the thalamus, elbow flexed, legs extended
Decerebrate response- midbrain lesion elbow & forearm extension, leg extension
Irreversible Loss of Brainstem Function:
apneic coma
PCO2 > 60
Negative corneal, pupillary, gag, negative OVR/OCR, with + Doll’s
W/o underlying metabolic or drug induced etiology
Unit 4 Headache, Neck & Back Pain
Tension HA usually after age 20 female > male, non throbbing bilateral occipital head pain “like a tight band around head”, not ass’d with N/V, prodromes, or auras. Chronic, frequent, sometimes involving tension in scalp or neck muscles, and may overlap with migraine type HA
RX: ASA, NSAIDs, ergot derivatives,
Prophylaxis: relaxation, PT, psychotherapy or TCA, SSRI’s, propranol
Migraine HA early onset, females> males or + Family Hx, pulsatile unilateral pain often ass’d with N/V, photophobia, and aura (intracranial vasoconstriction) vs HA (extracranial vasodilation), auras can be visual alterations such as hemanopic field defects, scotomas, scinnilations. Diagnostic Test: compression of ipsilateral carotid or superficial temporal artery may decrease severity of HA. Precipitating factors tyramine, nitrites, phenyethylamine, MSG, fasting, caffeine, emotion, menses, OCPs, nitroglycerin, bright lights.
RX: NSAIDS, ergot derivatives
Prophylaxis: propanol, TCA, methylsergide, CCB
Cluster HA - Men> women, > 25 year age @ onset, 10 mins-2hrs duration, Awakens patient at night, burning sensation lateral aspect of nose, pressure behind eye, lacrimation, nasal d/c, & Horner’s are common w/these. Precipitated by Etoh and vasodilating drugs, smoking.
Abortive: Sumatriptan SQ, 100% O2, dihydroergotamine SQ
RX for Chronicity: Prednisone, Indomethacin
Prophylaxis: ergotomine, methysergide, CCB

Trigeminal Neuralgia (Tic douloureux)
facial pain syndrome of CN V roots possibly due to arterial compression of nerve roots
V2 V3 unilaterally lighting like jabs of pain, spontaneously cease w/ sensory triggers on face by touch, cold, wind, talking or chewing
Simillar pain w/ MS or brainstem tumors possible
RX: Tegretol or Posterior Fossa decompression surgery
Temporal Arteritis
subacute granulomatous inflammation of temporal or vertebral artery
HA, severe boring temporal face pain, > women over 50, uni or bilateral
50% of untreated pt will develop blindness due to opthalmic artery involvement
DX w/ biopsy, ESR > 100
RX: prednisone for 1-2 years
Cervical Spondylosis
can include neck stiffness, pain in arms, segmental motor/sensory deficit in arms, UMN in legs, cervical disc degeneration and herniation, secondary ossification, and osteophytic outgrowths
can involve > 1 nerve root & be uni or bilateral
presents w/ neck pain, limited head movement, occipital HA, radicular pain, sensory change in arms/legs
C5, C6 commonly involved
DX: Xray, myelography, CT/MRI
DDX: myelopathy of MS, motor neuron disease, SCD, cord tumor, syringomyelia, hereditary spastic paraplegia
RX: cervical collar, surgery
Radicular Syndrome
localized to one or more nerve roots (segmental paresthesias & numbness & weakness & reflex changes)
exacerbated by coughing, sneezing, or other increases in ICP
C5 C6 Radiculopathy
weakness in deltoid, supra/infraspinatus, biceps, brachioradialis
pain & sensory loss in shoulder, outer arm and forearm
reflexes : decreased biceps and brachioradialis
ass’d myelopathy UMN weakness in 1 or both legs, change in tone or reflex, PC or STT sensory defects
L5 S1 Radiculopathy
weakness dorsiflexion of foot, toes, eversion, plantar flexion,
Reflexes : decreased ankle jerk
Spine movement restricted w/ local back tenderness, decreased straight leg raising
Low Back Pain
Trauma
-Musculoskeletal pain w/ lumbar muscle spasms, decreased spinal movement, DX: Xray to r/o vertebral fractures RX: bed rest, local heat, NSAIDs, and muscle relaxants
Prolapsed Lumbar intervertebral disk
most common L5-S1 and L4-L5
usually follows normal activity or strain, can be related to trauma
can cause radicular pain, segmental motor/senosory deficits, & sphincter disturbances
pain reproducible upon percussion over spine & passive straight leg raising
Pelvic exam, rectal exam, & Xray to r/o other diagnosis

RX: analgesics, diazepam, bedrest w/ PT , if not fixed consider CT/surgery, etc
Lumbar Osteoarthropathy
later in life an increase in activity leads to pain
mild Sx Tx w/ surgical corsett & severe treat w/ surgery
can present as root/cord pain, spinal stenosis (intermittant claudication of the cord or cauda equina) requiring surgical compression
Ankylosing Spondylitis
backache and stiffness, progressive limitation of movement, young men HLA B27
RX: Pain – ASA, indomethacin, PT, postural excercises
Neoplasms
suspect if symptoms are persistent and worsen despite bedrest
MRI to r/o mets, cord compression and cauda equina
Infectious
TB, pyogenic, cocci, of the vertebra or disc
LABS: increased WBC’s, increased ESR
RX: surgical debridment, long term (IV) antimicrobials, drainage
Osteoporosis
vertebral compression fractures
RX: NSAIDS, adequate activity, diet, HRT for post menopausal women
Paget’s disease of the spine
increased alk phosphatase w/ a NL Ca++ and NL PO4
urine hydroxyproline and urine Ca++ increase w/ active disease
Xray show increased density and expansion of bone, possible fissure fractures
RX: high Protein diet, Ca++, Vit C, Vit D, Anabolic hormones, calcitonin, bisphosphates, mithromycin to decrease osteoclast activity.
Congenital Anomalies of Lower Back/Spine
Spinal Dysraphism
defect in spinal fusion presenting w/ pain, neurologic deficit in 1 or both legs & sphincter disturbances
Spinal Stenosis
can lead to syndrome of neurogenic claudication later in life
Arachnoiditis
severe pain in back and legs due to inflammation and fibrosis of the arachnoid area
Referred Pain
Disease of hip joints, back & thigh pain w/activity w/ limitation of movement, + Patrick’s sign (pain on external rotation), & Xrays show degeneration of hip joint
Other causes: Triple A, Cardiac ischemia, visceral/retroperitoneal masses, GU disease
Unit 5 Movement disorders
Postural tremor - tremor w/ sustained posture continuing w/ movement w/o increasing in severity
physiological 8-12 Hz commonly w/outstretched hand
enhanced physiological – as above but worsened w/ stress, anxiety, thyroidtoxicosis
Familial Benign essential tremor- AD inheritance involving 1 or both hands, head or voice w/sparing of legs, medically treated w/ beta blocker Propanolol or anticonvul. Primidone
Drug induced, metabolic d/o (Wilson’s) or cerebellar d/o also produce tremor
Intentional tremor - tremor w/ activity, due to lesion in SCP or as a drug toxicity and can result in fxnl disability, treament is surgical procedure= sterotactic surgery of VLN of the thalamus; CEREBELLAR
Resting tremor - tremor w/o movement, characteristic of Parkinson’s but can be idiopathic or 2ndary to heavy metal poisoning (Pb+/Hg+) or Cu+ (Wilson’s disease); BASAL GANGLIA

Chorea - rapid, irregular, involuntary muscle jerks in various parts of body
Huntington’s disease- due to loss of neurons in caudate nucleus & putamen
Drug induced / SE of Dopa agonists- levadopa, antipsychotics, lithium, phenytoin, OCP’s
Vascular- vasculitis d/o, ischemic/hemorrhagic stroke, subdural hematoma
Static encephalopathy (Cerebral Palsy) secondary to anoxia, hemorrhage, trauma, or kernicterus
Dyskinesia - movement disorder that w/excessive abnl, involuntary movements i.e. tremors, chorea, hemiballismus, myoclonus, dystonia, tic, or athetosis w/ various etiologics including hereditary, vascular, or drug induced.
Isolated Focal dystonias - often treated with Low dose Levadopa, trihexphenidyl (anti cholinergic Artane), diazepam, baclofen or tegretol or surgically w/ stereotactic thalamotomy esp. w/ unilateral limb dystonia
1.
Blepharospasm- involuntary closure of eyelids
2.
Oromandibular dystonia
3.
Torticollis- neck twisting, tx as above w/ botox injections possible CNXI sectioning
4.
Writers cramp- drugs not very therapeutic, alternating hand therapy, possibly botox
Important points in evaluation of Movement disorders
Age & Mode of Onset: Infancy think birth trauma, kernicterus, anoxic damage or CP, inherited d/o
Childhood common for tic development, Tourette’s
Abrupt onset think drug induced or ischemic event
Slow onset think degenerative disease
Drug & Medical Hx: anti psychotics(phenothiazine/haldol) commonly cause tardive dyskinesia
Levadopa (dopaminergic agonists) can cause chorea
Lithium, TCA, valproic acid (depakote), bronchodilators can cause tremor
SLE, Thyrotoxicosis can induce chorea
AIDS can cause tremor, chorea, dystonia, hemiballismus
Family Hx: History of demyelinating d/o
Huntington’s disease
Idiopathic Parkinson’s Disease
loss of pigementation (cells) or presence of intracytoplasmic Lewy bodies in the substantia nigra or other brain stem centers such as the globus pallidus, putamen, spinal cord or sympathetic ganglia
imbalance between dopamine and Ach allows excess Ach to excite the inhibitory (GABA) release in the globus pallidus inhibiting the thalamus and cortex causing bradykinesia
5 Features of PD
bradykinesia, rigidity, resting tremor, masklike facies, stooped posture w/shuffling gait
dx is clinical
Mainstay Treatment of Parkinson’s disease
1.
Early PD- no drug Rx
2.
Progressive/symptomatic Rx
Levadopa/Carbidopa (Sinemet) - helpful for hypokinesia SE: N/V, hypotension, chorea, restlessness, confusion
Bromocriptine/& Pergolide (dopamine agonists)- ergot derivative, SE: psychiatric , Contraindication in pts w/ psychiatric d/o’s, MI, severe peripheral vascular disease, and active PUD
Amantadine - antiviral that increases the release of dopamine SE: restlessness, confusion, skin rash, edema, arhythmias
Anticholinergic (muscarinic agonists) – to alleviate tremor & rigidity
Ex’s hexyphenidyl, benztropine, procyclidine, phenadrine
SE’s dry mouth, urinary retention, constipation, defective pupillary accomodation & confusion

Parkinson Plus Syndromes
1.
Shy-Drager Syndrome- Parkinson’s with ANS instability & other neurological involvement
2.
Cortical Basal Ganglionic Degeneration- Parkinson’s w/ sensory loss, apraxia, focal reflex myoclonus w/asymmetric symptoms & no ANS instability or cognitive loss. Some Pt’s respond to sinemet
(levidopa/carbidopa)
Tardive Dykinesia: Pt w/ abnormal choreoathetoid movements usually of face or mouth in adults or limbs in kids that can develop w/ long term Rx w/ antipsychotics (anti-dopaminergics)
Neuroleptic Malignant Syndrome : Patient develops rigidity, fever, altered mental status, and autonomic dysfunction over 1-3 days of antipsychotic treatments ESP’LLY WITH HALOPERIDOL , RX w/ dantrolene or manage symptoms with antipyretics, anticholinergics, antipsychotics lithium. DDx is infectious cause.
Unit 6 Motor and Sensory Deficits
Jaw - mandibular branch V3 3and pons
Biceps - Musculocutaneous and C5 , C6
Brachioradialis – radial and C5, C6
Triceps- Radial and C7, C8
Finger- Median and C8, T1
Knee- Femoral and L3, L4
Ankle- Tibial and S1, S2
Pyramidal System from Motor cortex to IC - medullary pyramid decussation to descend in CL CST : lesions here will cause difficulty in fine motor movements. (UMN)
Extrapyramidal System - UMN input from Basal Ganglia or cerebellum : lesions here will have uncoordinated rate, rhythmic, and irregular amplitude movements
LMN motor fibers are cranial nerves or peripheral nerves
Appearance
Fasiculations are to LMN injuries (or anterior horn disease) as flexor and extensor spasms are to UMN.
Psuedohypertrophy is usually due to myopathies w/ replacement of muscle by adipose or other tissue.
Tone
Two types of hypertonia- Spasticity (clasp knife-velocity dependent w/ arm F>E and legs E>F most likely due to UMN damage) & rigidity (lead pipe- seen in passive movement affecting all muscles equally most likely due to BG/cerebellar lesion with cogwheeling superimposed )
Paratonia- seen in pts with frontal lobe or diffuse cerebellar disease where patient is unable to relax and will move limbs as examiner does.
Power (or weakness 0 –no contraction 1 flicker 2 active w/ gravity eliminated 3 active but no resistance 4 active to gravity and resistance & 5 nl)
UMN weakness pattern affects Extensors and Abductors in the ARMS and flexors in the legs.
LMN weakness pattern of supplied muscles at SC, root or peripheral level with distal > proximal
Proximal more than distal suggests a myopathy or NMJ
Variability in pattern of severity and distribution over time suggest Myasthenia gravis/Lambert Eaton syndrome.
Reflexes
Areflexia- root lesion, or peripheral neuropathy or early UMN disease, deep coma
Hypereflexia- (clonus)- rhythmic contractions in response to a stretch

Lateralized asymetrical of reflex responses (UMN disease)
Focal reflex deficits relating to root, plexus, or peripheral nerve lesions
Loss of distal DTR common in polyneuropathies & can be normal finding in elderly.
Gaits
Apraxic (dominant frontal lobe d/o- hydrocephalus, dementing processes, w/o weakness or coordination problems) usually can’t stand unsupported, feet glued to ground, unsteady short stepped gait
Hemiparetic w/ circumduction- unilateral lesion of CST pt tilts at waist and swings affected leg around
Scissoring- w/severe bilateral spasticity, legs brought stiffly forward & adducted w/ compensatory trunk movements (UMN sign)
Parkinsonian gait- small steps taken at a increased rate (festination), problems with starting and stopping, forward stooping, reduced arm swing
Steppage gait in persons w/ impaired sensation.
UMN SYNDROMES (damage to cortical areas where UMN orginate pyramidal & extrapyramidal CST)
hypertonia “spasticity”
arms flexed (w/ weakness of extensors and abductor) legs extended (w/ weaker flexors)
hyperreflexia “sustained or nl clonus ”
changes in gait
+ Babinski
Radiculopathy lesions affecting specific nerve roots yielding characteristics changes in muscle innervated, location of sensory and reflex changes, dermatone distribution
Neuropathy - pathology of a nerve that causes weakness in innervated muscles (distal >proximal) w/ a decreased reflex or sensory change, fasiculations and muscle wasting can occur later in disease
Myelopathy - lesion affecting spinal cord
Myopathy d/o affecting the muscles, usually presenting with weakness in proximal area vs. distal, w/ NO sensory loss, no sphincter disturbances, nl abdominal and plantar reflexes, with muscle wasting & decreased/absent reflexes only late in disease
ALS
Pure motor syndrome mixed UMN & LMN signs w/ NO sensory deficit usually beginning in the limbs
(40%) c/o weakness, cramping, twitching, stiffness, etc in upper extremites and (40%) c/o of the same type of stuff in lower extremities
(20%) present with bulbar signs; which has a worse prognosis
Progressive, fatal w/in 3-5 yrs, mainly due to respiratory problems, infections
Clinical Dx., CSF is normal, no sensory change or mental dysfunction
Rx of Symptoms
Drooling- treat w/ anticholinergics
Mobility – walkers, braces
Contractures- prophylaxis PT
Myasthenia Gravis
occurs at ANY age; Females > males & often ass’d w/ Thymomas, thyroidtoxicosis, or SLE
characterized by fluctuating weakness of voluntary muscles w/ a predilection for extraocular muscles
(bilateral opthalmoplegia) and other CN muscles (massetor, facial, laryngeal, pharyngeal) but can get limbs & diaphragm as well

Pt present w/ ptosis, diplopia, difficulty swallowing or chewing, nasal voice, weak limbs and respiratory difficulties w/o sensory changes & w/o reflex changes
autoimmune etiology- Ab’s against the Ach receptor at the postsynaptic NMJ causing a relapsing, remitting course
can have insidious onset or become symptomatic in times of stress (infection, menses, pregnancy)
drug induced onset w/quinine, quinidine, procainamide, propranolol, Lithium, phenytoin, PCN & aminoglycosides
Dx is clinical and the edrophonium (anticholinesterase drug- Tensilon) test is useful to check for improvement right away. If improved, prescribe a longer acting pyridostigmine (Mestinon)
Other Rx’s & tests
Other anticholinesterase drugs(Mestinon), corticosteroids, azathioprine, plasmapharesis, IVIG
CXR for thymomas, or thymic hyperplasia w/ thymectomy if indicated
EMG
Symmetric Polyneuropathies:
Guillen – Barre Syndrome-
weakness usually begins in legs, may have sensory and autonomic complaints
often follows infective illnesses, innoculations, or surgical procedures. May be associated with camplobacter jejuni
speed and progression variable but can be fatal
Dx: acute onset w/progressive weakness of > one limb up to 4wks, symmetrical, distal areflexia w/ proximal hyporeflexia, mild sensory changes, CN VII involvement, autonomic dysfunction, with recovery beginning 4wks after onset.
Tests: CSF w/ increased protein BUT NO Cellls; EMG shows slowing
Rx’s: plasmaphoresis, IVIG (400mg/kg/d X 5d)
Prognosis: Sx’s decrease after 4 weeks, 75% recover, 25% have neurodeficits w/ 5% dying acutely
Critical Illness Polyneuropathy-
pt w/ sepsis or multi-system failure
wasting of extremities w/ absent DTR’s and sensory changes
Diptheria Polyneuritis-
neurotoxin produced by C. diptheria 2-3 wks following a palate or muscle infection
within 4-5 weeks pupillary response impaired
1-3 months generalized sensory polyneuropathy; weakness proximally> distal
Dx. CSF w/ increased protein, pleocytosis & EMG showing decreased conduction
Rx Antitoxin + 2 weeks of PCN
Paralytic Shellfish Poisoning -
poison blocks Na+ channels causing a rapidly progressing sensory & motor ascending paralysis
Porphyria-
weakness usually proximal > distal; beginning in upper extremities and later involving leg and trunk
decreased or absent DTR’s, sensory changes
also causes abdominal pain, psychosis, fever/chills, HTN, hyponatremia, peripheral leukocytosis
Arsenic/ Thallium poisoning-
sensorimotor polyneuropathy w/ GI disturbance
distal > proximal & legs > arms
Organophosphate poisoning-
cramping pain to distal numbness progressing to leg weakness & decreased DTR
sensory changes 1 st in legs then arms
Sensory Disorders

Complete loss of touch= anethesia of pain= analgesia
Partial loss of touch= hyesthesis
Increased sensitivity= hyperesthesia of pain= hypalgesia of pain= hyperalgesia/hyperpathia
Light touch= ipsilateral posterior columns (large fibers) to medial lemiscus of brain and on the contralateral anterior spinothalamic tract
Pinprick & Temperature= ipsilateral lateral spinothalamic tracts for 2-3 segments after entry and then cross over infront of central canal
Deep Pressure= evaluated on tendons (achilles)
Vibration= 128 Hz tuning fork on bony prominence, often decreased in elderly below the knees
Joint Position= passive movement of DIP joints thought to be carried in fibers also in the posterior columns
Complex sensory tests
Romberg’s Test= + w/ unsteadiness to evaluate impairment of joint sense in legs ( tabes dorsalis )
Two point discrimination = depends on intergration between the CNS & PNS and sensory compenent of the area stimulated. Threshold is 4mm on fingers to several cm on back. If PNS is intact w/decreased two point discrimination d/o in sensory cortex (CL parietal is suggested ).
Graphesthesis, Stereognosis, & barognosis = able to identify a number traced in palm, shapes presented or pressures applied in area w/ normal sensation implies problem in CL parietal lobe .
Bilateral sensory discrimination (EDSS) = neglect/or decreased reaction to 1 side of stimulus suggest CL cerebral lesion
Sensory changes often develop well before onset of sensory signs and should not be considered psychogenic.
Peripheral nerve lesions:
Mononeuropathy = not usually noticed b/c of overlap but can be caused by compression lesions that preferentially involve the large touch fibers.
Polyneuropathy= symmetric and distally> proximally (glove and stocking sensory loss) feet before hands usually. EX’s Tangier disease (metabolic AR d/o w/ little or no HDL) tends to involve small pain & temperature fibers . Can also involve motor and reflex changes .
Distal axonpathies > myelinopathies ; including acute idiopathic GBS, CIDP, infective (AIDS, leprosy, diptheria, sarcoid), vasculitic ( PAN, RA, SLE), paraneoplastic syndromes, drug induced ( alcohol, INH, Dilantin, dapsone, vincristine, etc.), toxins, heavy metals (Pb), metabolic and nutritional neuropathies (DM, hypothyroid, uremia. B 12), entrapment, & hereditary neuropathies often w/ motor involvment (metachromatic leukodystrophy, Krabbe’s disease, Freidreich’s ataxia,
Fabry’s, Refsum’s, etc)
Radicular lesion/Root involvement= impairment of a segemental cutaneous pattern
Root + pain suggests compression lesion
Loss of reflexes at specific root levels C56 bi/brachio C78 tri L34 knee and S1 ankle
W/ weaknes and muscle atrophy= suggest anterior root involvement
Central Cord lesion = syringomyelia , cord tumors , loss of P & T 1 st , bilateral , segmental, and possibly w/ LMN weakness & pyramidal or PC deficit below level of lesion.

Anterolateral cord lesions= CL impairment of P & T below level of lesion, with sacral segments involved first with extramedullary lesions and can be spared in intrinsic or intramedullary lesions.
Anterior Cord lesions : CL impairment of P & T below level of lesion w/ LMN weakness of paralysis of muscles supplied by the segment due to damage of the anterior horns
Posterior Column Lesion = tight or bandlike sensation at level of the lesion w/ paresthesias (electrical shocks) shooting down extremities on neck flexion (Lhermitte’s sign).
Loss of vibration and position sense w/ preservation of sensory.
Cord Hemisection or Brown-Sequard Syndrome= ipsilateral pyramidal deficit (UMN signs) w/ disturbed vibration and positional sense w/ CL loss of P & T 2-3 segments below the lesion
Crossed Sensory Deficit in Medullary lesions = P & T lost in CL limbs w/ Ipsilateral facial pain & T lost
Wallenberg type
Brain Stem lesions = usually sensory combined w/ motor, cerebellar signs, & CN palsies
Pons= P&T lost in CL limbs and trunk
Medulla = P & T lost in CL limbs and trunk w/ ipsilateral P & T loss of facial sensation (spinal
Trigeminal nucleus) (Wallenberg syndrome)
Medial Lemiscus= CL loss of touch and propioception or w/ upper brainstem involvement
Complete CL loss of sensation
Thalamic lesions = CL impairment of all forms of sensation except in some cases where there is a painful sensation with any stimulation (Dejerine-Rousy syndrome) This can result from lesions of white matter of the parietal lobe or SC. (also know as thalamic pain syndrome).
Sensory Cortex Lesions : CL impairment of discrimatory sensory function usually worse distally more than proximally
Psychogenic disturbances could be conversion disorder & are usually cutaneous.
Non organic tends to surround an area defined by surface landmarks, sharp margins & commonly stops at midline
Organic does not usually extend to midline b/c of overlapping innervation and has surrounding areas of altered sensation.
Examples of types of Peripheral Neuropathies
Metabolic: DM, hypothyroidism , acromegaly, uremia, liver disease, vit B 12 def’y, hyponatremia, hypoglycemia
Infectious: AIDS, TB Leprosy #1, diptheria, sarcoidosis, sepsis, multiorgan failure
Hereditary: HMSPN, Friedreich’s ataxia, Familial Amyloidosis, Porphryia, Krabbe’s, Tangier’s
PN’s associated with PAIN: DM, Etoh, porphyria, Fabry’s, amyloidosis, HSN, paraneoplastic senosry neuropathy.
Entrapment Neuropathies :
Carpal Tunnel Syndrome: compression of median nerve @ writst
often during pregnancy, or seen w/ trauma, degenerative arthritis, myexedema, acromegaly, amyloidosis
pain & paraesthesia of median n. distribution of hand (thumb, index, middle, & lateral ½ of ring) can radiate up to neck and can keep pts awake at night, weakness and thenar atrophy may occur later
Dx. Tinnel’s sign (pressing over median nerve) & Phalan’s sign (wrist flexion) both positive
EMG
Rx: corticosteroids, splint, surgery
Ulnar nerve palsy: compression @ elbow

may result from ext.pressure, entrapment @ cubital tunnel or from cubitus valgus deformity
nocturnal pain in little finger & ulnar border of hand +/- pain at elbow, possible weakness/sensory Sx’s
Rx: surgical decompression
Peroneal Palsy: secondary to trauma or pressure @ head of fibula
weakness or paralysis of foot and toe extension/foot eversion, impaired sensation over dorsum of foot
& lower ant. Aspect of leg, ankle DTR’s are present
Rx: supportive
Femoral Nerve Palsy: L3,L4 ass’n w/ DM, vascular ds bleeding diathesis, or retroperitoneal neoplasms
weak quadriceps, decreased patellar reflex, sensory changes of ant/med aspects of leg
Rx: treat underlying disease
Herpes Zoster -
viral d/o that causes an inflammatory rxn in dorsal root ganglion or CN nuclei, in the affected root, or in nerve itself, can also be in CSF
intial c/o burning or shooting pain w/in dermatome with rash 2-5 days later, rash resolves with scars and possibly post herpectic neuralgia
common sites: thoracic dermatome, V1 of CNV which may lead to corneal scarring and anesthesia
Ramsey Hunt syndrome CNVII palsy w/ herpectic eruptions in ear, palate, pharynx and nose
Rx: Acyclovir or steroids for Sx’s and tegretol 1200 mg/d, phenytoin 300mg/day, and amitryptiline 10-
100 mg q hs.
Syringomyelia-
Communicating ( hydrodynamic d/o of CSF pathways) opening between central cord and cavity
Non Communication- cystic dilation of cord not communicating with CSF pathways
severity is site dependent, mainly w/ impaired P & T at that level with intact light touch
sensory loss commonly seen by presence of painless skin ulcers, neuropathic joints, edema, scars, etc
muscle wasting @ level of lesion with Extrapyramidal signs and sphincter disturbance possible
pyramidal lesion w/ gliosis or compression of CST
scoliosis is common
decreased DTR below lesion and Increase above lesion
Friedrich’s Ataxia- idiopathic degenerating disease of cerebellar ataxia
AR chrom 19 begin’s in childhood
Demyelination of Spinal cerebellar tract, posterior column, dorsal roots and neurons in clark’s nucleus
Large axons of periferal nerves as well as cell bodies of sensory nerves, and dorsal root ganglion
Sx’s: Gait ataxia, progression to involve all limbs, dsyarthias, w/2ndary features impaired flexor
/extensory response, pes cavus, scoliosis, and cardiomyopathy.
Unit 7 Multiple Sclerosis
CNS demyelination Signs in MS:
Demyelination slows AP’s or blocks them and effects heavily myelinated tracts i.e. optic nerves, posterior columns, corpus callosum, brainstem pathways, and spinal cord.
Can present w/focal weakness, numbness, tingling or unsteadiness in a limb, sudden loss or blurring of vision in 1eye (optic neuritis), diplopia, disequilibrium, or bladder fxn disturbance. Some patients present with mainly UMN sx’s as acute to gradual spastic paraparesis w/ sensory deficit.
Mechanism considered to be autoimmune, with hypersensitive T cell (or IgG’s) attacking myelin &
CNS myelin producing cells oligodendrocytes, HLA DR2 genetic relation, women > men, ages 20-40, and increased exacerbations with heat which sensitizes the Na+ channels that are responsible for AP conduction
Impaired/blocked conduction can result in gliosis
6 common clinical presentations of MS

1.
optic neuritis- tested w/ swinging light test shows Marcus Gunn pupil or pupil w/ afferent defect which will constrict less markedly w/ direct illumination and also have decrease in color vision a sign of retinal involvement
2.
INO- demyelination of the MLF clinically seen as MR palsy or diplopia sign of Brainstem disease and if not MS DDx includes brainstem encephalitis, tumor, syringomyelia, drug intoxication, Wernicke’s
3.
Disequilibruim- posterior column (+ Romberg’s test)
4.
Urinary incontinence or frequency, ANS dysfunction that causes spasms or retention
5.
Focal weakness (bilateral paraparesis of both legs)
6.
Paraesthesias- numbness or tingling or dyesthesias- painful sensation from a non painful stimulus allodynia
7.
Spasticity- increased tone, clasp knife effect w/ velocity dep’t passive movement, UMN lesion
Clinical criteria for Dx of MS
1.
2 signs or symptoms separated in time and space
2.
clinical picture w/ history and elimination of other possible cause for symptoms
3.
MRI (T2 w/contrast) -w/ evidence of plaques (areas of demyelination in the white matter;commonly periventricular)
Paraclinical supporting tests
1.
LP w/ CSF showing increased IgG; oligoclonal bands (+ in 90% of pts)
2.
VEP, BAER, SSEP evoked potential showing slowing
Other conditions or DDx for MS
1.
isolated Optic neuritis (70% will go on to develop MS later)
2.
transverse myelitis (Brown Sequard Syndrome)
3.
vasculitis (SLE, Sjorgens, etc)
4.
AIDS
5.
Lyme disease (bilateral Bells or CN VII palsy)
6.
Inherited spinocerebellar degenerations (Freidrich’s Ataxia)
7.
Adrenoleukodystrophy/Metachromatic leukodystrophy
8.
CNS mass lesion (more likely if focal defecits clinically)
Prophalaxis drugs (ABC’s of MS)
1.
Avonex (beta interferon 1a)
2.
Betaseron (beta interferon 1b)
3.
Copaxone (glatiramir acetate) alters or interferes w/ T cell response to myelin w/ SE of flu like syndrome, increased spasticity & side reactions w/ betaseron
Rx for acute exacerbations
IV methylprednisolone (Solu-Medrol) 500-1000 mg/d, IVIG, plasmaphoresis
Management of MS
ACTH- 80 U IM x 1wk, tapered for 2-3 wks
Steroids: Methylprednisolone 15-20 mg/kg/d IV x 3days, taper 2 wk Prednisone 60-80 mg/day PO x 1 wk, taper 2 wks Dexamethasone 16 mg/d x 1wk
Immunosuppressants: Cyclophosphamide, azathioprine
IVIG, plasmapharesis
PT/OT & speech therapy
Spasticity- Baclofen (GABA agonist), Tizanidene alpha agonist(zanaflex), Dantrolene, Diazepam
Neuropathic Pain- TCA amitriptyline (elavil), or anti-convulsants gabapentin (neurontin), dilantin, tegretol
Fatigue- pemoline (cylert), amantadine (Dopa agonist), fluoxetine
Unit VIII DEMENTIA
Dementia- progressive deterioration in mental function that interferes w/ ADL’s
Need 2 or more of the following:

-Defecits of memory, language, visualspatial skills, calculation, apraxia, agnosia, abstract reasoning, behavioral component
Persistance of deficits is the differentiating feature from delirium.
Evaluation duration, progression, risk factors, ass’d neurological findings, Hx of psychiatric disease, head injury, or FHx of neuro/psychiatric disease
DX work up: CT/MRI, SPECT/PET, EEG, LP, metabolic panel w/ CBC
Alzheimer’s most commonly diagnosed form of dementia
risk factors= age, FHx, head trauma w/ LOC
present w/ loss of ST memory, language, orientation, & judgement
progresses over 2-20 year period ultimately involving all functioning
pathological dx senile (amyloid) plaques, NF (tau microtubule protein) tangles, neuronal degeneration
association cortex in parietal, temporal and frontal lobes particularly affected
loss of cholinergic activity in forebrain: nucleus basalis of Meynert
dx is one of exclusion, with diffuse cerebral atrophy possibly seen on CT/MRI
PET scan may show regional hypoperfusion in parietaltemporal region, EEG w/ slowing
Apo E4 Genotype testing & CSF levels of high Tau and lowAmyloid have poorer prognosis
RX: acetylcholinesterase inhibitors (Cognex & Aricept)
Symptomatic treatments: LD benzo’s, neuroleptics, AD’s
Genes involved in SDAT chrom 21 amyloid, chrom 14 is presenilin, chrom 1 is presenilin 2, 19 is Apo
E w/ E4 homozygotes at highest risk , Apo E2 may have protective benefit in caucasians
Multi Infaract Dementia
elements of both cortical and subcortical dementia
stepwise progression, psuedobulbar effect w/ impossible localization of a single focal lesion
DX: CT can miss small infarcts & MRI is more sensitive
Non invasive or invasive vascular studies are useful
RX: antiplatelets, anticoag, decrease risk factors
Infectious Dementia
resulting from meningitis or encephalitis
general paresis of the insane “treponemen pallidum” neurosphyllis delayed onset up to 30 yr, RX w/
PCN
chronic meningitis agents: syphillis, crytococcus, TB, borellia, other fungal/ parasites possibly presenting w/ hydrocephalus
AIDS dementia complex – HIV 1 presents w/ psychomotor retardation progressing to global dementia consider concurrent infections; cryto, PML
Herpes Zoster Encephalitis- diffuse slowing on EEG
CJD disease w/ characteristic EEG pattern of periodic complexes
DX : RPR, VDRL-ABS, lyme serology, MRI/CT, CSF culture
RX: acyclovir for herpes, Ab’s
Normal pressure Hydrocephalus (NPH)
Communicating & non communication Hydrocephalus are both able to produce dementia
Nl CSF pressure 100-200 mm H20
NPH can be caused by SAH, CSF infections or idiopathic
Present w/ ataxia, urinary incontinence, and dementia
DX: CT/MRI showing dilation of ventricles, or radionucleoside cisternography
RX: ventricular shunting improves 50% of cases
Dementia in Extra Pyramidal Syndromes (UMN Globus pallidus & cerebellum)
Parkinson’s -- can present w/ tremor, cog-wheel rigidity, bradykinesia, shuffling gait, masked facies
RX: sinement, amantadine, bromocriptine, selegelline (MAO B inhibitor)
Diffuse Lewy Body disease
Huntingtons- choreoathetosis w/ positive FHx
RX: anti dopaminergic haloperidol & risperidone (antipsychotics)

Wilsons- deposition of Cu++ seen on CT/MRI, genetic testing, serum copper levels
Progressive Supranuclear palsy- paralysis of vertical gaze and axial rigidity
Corticalbasilar degeneration- apraxia & alien limb phenomenon
Random questions
Which extrapyramidal syndrome presents with dementia , paralysis of vertical gaze and axial rigidity?
Progressive supranuclear palsy (PSP)
Which extrapyramidal syndrome that has dementia, choreoathetosis, can be sometimes diagnosed with
MRI, and whose motor symptoms often respond to anti-dopaminergic agents such as Haloperidol and risperidone?
Huntingtons disease, AD genetic disease, chromosome 4, atrophy of caudate nucleus
Which disease of dementia has the histopathological change of neuronal granulovacuolar degeneration, especially in the nucleus basalis of Mey nert & favors the association cortex in the parietal, temporal, and frontal lobes and can be diagnosed sometimes on a volumetric analysis of the hippocampal/temporal regions?
Alzheimer’s Disease , also with senile plaques and NF tangles but too obvious to include in the question.
Associated with chromosome 1 (presenilin 2), 14 (presenilen 1), chromosome 19 (Apo E) and chromosome
21 (APP-amyloid precursor protein).
Which disease can be symptomatically treated with Cognex and Aricept , along with low dose benzodiazepines, AD’S trazodone, or neuroleptics for behavioral changes or paranoia?
Alzheimers
Which allele is associated with higher LDL and familial and sporadic AD?
Apo E4, and combined with head injury it may increase the risk ten fold
Which protein that is associated with microtubules is elevated in AD w/ a 90% specificity?
Tau
Is beta amyloid, the protein ass’d with neuritic plaques increased/decreased or nl in the CSF of pt with AD?
They are decreased in pt’s with AD and if they are elevated in a patients CSF it can rule out AD.
High Tau > 420 pg/ml and low Ab <1240 is diagnostic for AD
Which lobes are involved in Pick’s Disease?
Frontal and Temporal Lobe (FTD) inappropiate bx W/O the three A’s No amnesia, NO aphasia, NO agnosia, ex. Is Kluver-Bucy syndrome
Multi-infarct dementia’s have what type of characteristic presentation?
Progressive, psuedobulbar, or w/possible focal deficits in high risk people, most commonly due to subcortical lacunar infarcts
What is the preferred evalation for dx of MID?
MRI or vascular studies
Infectious dementia can be caused by which key organisms?
Treponema pallidum, TB, cryptococcus, borrelia, etc.
Which studies are done to rule out additional causes of dementia in patients with HIV 1 ass’d dementia?
An LP to check for crypto or imaging to r/o PML, & if non AIDS pts Creutzfeldt-Jakob disease or
HSV
A patient presents with a triad of dementia, gait ataxia and incontinence w/ a history a recent MVA what is a likely diagnosis?

NPH (between 100 & 200) secondary to a subarachnoid bleed, caused by infection or AVM
Contusions of the grey matter in the orbitofrontal and temporal lobes along with diffuse axonal injury to white matter structures can cause which syndrome in young people?
Post-traumatic dementia, often occuring after an MVA.
An elderly woman presents to the ER after falling with fluctuating levels of consicousness, impaired attention, and is irritable. What could be the cause?
Subdural hematoma.
Which lobe is least likely to give focal deficits if involved w/ a tumor producing dementia?
Frontal
What kind of paraneoplastic syndrome is caused mostly by lung, breast, ovarian, and testicular CA that presents with neurological signs such as amnestic syndrome, seizures, or an affective disorder up to two years prior to primary tumor is discovered?
Paraneoplastic Limbic Encephalitis
Depressive dementia is typical cortical or subcortical in nature?
Subcortical w/ Complaints of deficits or I don’t know or I can’t type answers
Ganser syndrome refers to what type of dementia?
Hysterical w/ some somatomotor symptoms like conversion reactions & may be frank malingering.
Which cortices are primarily involved in Alzheimer’s disease?
Temporoparietal which can cause fluent aphasias w/ comprehensive problems & frontal
Misc. stuff for the wards
Isolated Eye Findings
CNVI (Lateral Rectus)- affected eye deviates medially, head turns towards the lesion side
commonly presents as increased ICP
most common etiology in kids is pontine glioma
most common etiology in adults is Nasopharyngeal carcinoma (presents w/ sensory findings)
CN IV (Superior Oblique) - Most common cause of vertical diplopia, eye is up & in, head tilting to opposite, w/ straight line test arrow points to the lesion side.
most common cause is trauma or idiopathic
CN III lesion- ptosis, eye is “down & out”, dilated non-reactive pupils, cyclopegia (loss of PNS of CN III)
a diabetic ischemic infarct spares the pupil (the PNS fiber are on outer portion of nerve)
a compression lesion dilates the eye, painlessly and progressive (uncal herniation)
common etiologies are aneurysms, temporal lobe herniation, meningiomas in cavernous sinus
Painful Opthalmoplegias
Tolosa Hunt Syndrome, psuedotumor cerebri, inflammation in the cavernous sinus
Acute Bilateral Opthalmoplegias-
Wernicke’s, GBS, MG, TB meningitis, botulism
Psuedoparalysis of upward and downward gaze-
Thyroid disease, myxedema infiltration of ocular muscles IR & SR

Duane’s Syndrome- congenital absence of CN VI “ retraction syndrome” eyes are sunken due to cocontraction of MR & SO causes globe retraction
Intranuclear Opthalmoplegia- If on the left there is no Left eye Adduction when patient looks to the Right, and the nystagmus is in the unaffected abducting eye (Right beating nystagmus)
lesion is in the MLF
commonly associated with MS
Down beating nystagmus is always central in origin
Wernicke’s, Arnold Chiari malformation, lesion in the medullary/cervical region
Vertical Nystagmus on upward gaze
commonly due to a demyelinating, or vascular disease, tumor or w/ Wernicke’s
lesion in the pontine medullary region of brainstem
Red Glass Test for Diplopia
false image is always the furthest image and the visual field where the two images are furthest apart is the field of vision of the affected muscle i.e. if horizontal nystagmus is worse w/looking to the right it is most likely the R abductor (R CNVI) or the left adductor (L CNIII)
for polymonocular disease of diplopia that is non specific DDx should include MG or thyroid opthalmopathy (w/ this eye may be protuding)
IF diplopia does not go away with covering of the eye you can call Psych b/c it is not likely neurological!
A CN III, IV & VI palsy is probably due to a brainstem lesion vs. a peripheral cause such as tumor at base of brain, ischemic infarction, or aneurysms within the Circle of Willis.
Common Brain Tumors
Astrocytomas
most frequent & include Glioblastoma Multiforme, gliomas in BS (pontine gliomas in kids), and pilocytic
Oligodendroglioma
most likely cerebral, focal hemorrhages & calcifications, variable prognosis
Ependymoma
younger people 10-20’s; often presenting with hydrocephalus
most common in 4 th ventricle> lateral ventricles > third ventricle> aqueduct of Sylvius
Medulloblastoma
occur in the cerbellum w/in the 1 st two decades of life
dissseminate through CSF, neuroectodermal in origin
highly malignant but radiosensitive
Meningioma
most commonly appear in frontal hemispheres, near falx, the lesser wing of sphenoid, and near olfactory groove
usually solitary but can be multiple if ass’d with NF Type 2
whorled pattern on histology, psammoma bodies
Common Mets to Brain
Lung, Breast, Colon, Melanoma, & Renal
Psuedotumor Cerebri- obese females w/ increased ICP, taking OC’s, that present with throbbing headache, visual changes (peripheral blurring/decreased acuity), and have papilledema on exam.
benign intracranial HTN w/ diffusely increased ICP
often present w/diplopia with CNVI palsy
females > males
CT/MRI shows small ventricles
RX: decrease ICP w/ furosemide, CA inhibitors or surgical optic nerve sheath fenestration

For refractory cases prednisone can be used.
Major danger of not treating an elderly patient with steroids that presents w/ a throbbing, acute HA, jaw claudication, with a HX of Polymyalgia rheumatica, and a current ESR of 100 is loss of vision due to thrombosis of the opthalamic artery due to Temporal Arteritis.