Neuro Review Part 2

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    OSCE | Batch 2014

    The estimated amount of glucose used by an adult human brain each day,

    expressed in M&Ms: 250 Harpers Index

    Keshia Lourdes Duyongco

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    NOTE: Neurology will NOT be included in the Identification

    Exam.

    Case 1: The Teacher Case 2: The Businessman

    Case 3: The Brave Policeman

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    A 55 year-old high school teacher develops sudden

    weakness of her left arm and leg, and over the next 30

    mins, these limbs become even weaker.

    When she looks at herself in the mirror, she finds that thelower half of her face appears to sag, and with

    vocalization, there is less movement on the lower left than

    on the lower right side of her face.

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    Her medical records reveal the ff info:

    BP: 140/90

    FBS: 110 mg/dl

    LDL: 120 mg/dl

    Total cholesterol: 250 mg/dL

    Question1: What is your interpretation of the data?

    Stage 1 HypertensionDiabetes mellitus

    High LDL (desirable:

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    When she is seen in the emergency room 1 hour later, she

    has almost complete paralysis of the lower part of the left

    side of her face and left arm and leg, with an

    approximately equal degree of weakness in the face, arm,

    and leg.

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    Question 2: Where is the lesion that is responsible for her symptoms?(a) Right internal capsule

    (b) Left internal capsule

    (c) Upper brainstem

    (d) Cerebral cortex

    ANSWER: A

    The most likely location is the right internal

    capsule. This is because the corticobulbar

    and corticospinal fibers innervating the

    contralateral face, arm, and leg are close

    together in this location.

    These fibers are also close in the upper

    brainstem but the patient has no clinical signs

    suggesting brainstem disease.

    The lesion is less likely to be in the cerebral

    cortex because the representation of the

    face, arm, and leg are distributed over a

    very large region.

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    Corticospinal Tract Aka: pyramidal tract

    Origin:

    1/3 Primary motor cortex (area 4)

    1/3 premotor and supplementary motor

    regions (area 6)

    1/3 parietal/primary somatosensory area(areas 3,1,2)

    Passes through

    Posterior limb of internal capsule

    Decussation:

    Medullary pyramids (90% of the

    corticospinal fibers cross at this level and

    descend through the spinal cord as the

    lateral corticospinal tract) to innervate the

    muscles in the distal parts of the extremities,

    i.e. hands and feet

    10% do not decussate and descend as the

    ventral corticospinal tract

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    Corticobulbar Tract Terminates in the brainstem to supply the motor nuclei of

    the cranial nerves III, IV, V, VI, VII, IX, X, XI, XII NOTE: cranial nerve motor nuclei receive innervation from both

    cerebral hemisphere, and in most cases, the muscles they control

    cannot be contracted voluntarily on one side only.

    Both the lower facial nucleus, which innervates facialmusculature below the eye, and the hypoglossal nucleusreceive innervation from the opposite cerebral cortex that

    is much heavier than the innervation from the ipsilateralcortex. Thus, these muscles can be controlled rather independently on the

    two sides (try it! ), and a lesion of one cerebral hemisphereresults in weakness primarily on the contralateral side.

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    Nerve CN Function Type PEARLS

    Olfactory I Smell S

    Optic II Sight S

    Oculomotor III Eye movt (SR, IR, MR, IO), pupillary

    constriction, accommodation, eyelid opening

    (levator palpebrae)

    M

    Trochlear IV Eye movt (SO) M

    Trigeminal V Mastication, facial sensation (VI ophthalmic,

    V2 maxillary, V3 mandibular)

    B Jaw deviates toward

    side of lesion

    Abducens VI Eye movt (LR) M

    Facial VII Facial movement, taster from anterior 2/3 of

    tongure, lacrimation, salivation

    (submandibular, sublingual glands), eyelid

    closing (orbicularis oculi), stapedius muscle in

    ear

    B

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    Nerve CN Function Type PEARLS

    Vestibulocochlear VIII Hearing, balance S

    Glossopharyngeal IX Taste from posterior 1/3 of tongue,salivation (parotid), carotid body and sinus

    chemo- and baroreceptos, and

    stylopharyngeus (elevates pharynx and

    larynx)

    B

    Vagus X Taste from epiglottic region, swallowing,palate elevation, midline uvula, talking,

    coughing, thoracoabdominal viscera, aortic

    arch chemo- and baroreceptors

    B Uvula deviates away

    from side of lesion

    Accessory XI Head turning (SCM), shoulder shrugging(trapezius) M Weakness turning head tocontralateral side oflesion (SCM), shoulder

    droop on side of lesion

    (trapezius)

    Hypoglossal XII Tongue movement M Tongue deviates towardside of lesion

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    Question 3: Which artery supplies the involved area?(a) Anterior cerebral artery

    (b) Middle cerebral artery

    (c) Deep branches of MCA

    (d) Deep branches of ACAANSWER: C

    The internal capsule is supplied

    by the deep branches of the

    middle cerebral artery.

    Review of cortical distribution:

    ACA (Anteromedial surface)

    MCA (lateral surface)

    PCA (posteroinferior surface)

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    Question 4: What has happened to Ms. S?

    ANSWER:

    Clinical evaluation led to the diagnosis of ischemic

    infarction (stroke) because of cerebrovasculardisease resulting from diabetes mellitus andhypertension. An MRI study verified the localizationand diagnosis.

    She was treated with tissue plasminogen activator

    in an attempt to dissolve the clot in vesselsperfusing the internal capsule.

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    A 55 year old man develops a feeling of stiffness and

    clumsiness of his left hand, and when sitting still, he

    observes a tremor involving the wrist and fingers of this

    hand.

    About the same time, he also begins to scuff his left foot on

    the floor occasionally while walking.

    About 1 year later, the tremor has become constant, and

    he trips occasionally because of the misplacement of hisleft foot.

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    What is the most likely diagnosis?

    (a) Huntingtons disease

    (b) Parkinsons disease

    (c) Cerebellar disease

    (d) Cerebral Palsy

    ANSWER: B

    The patient described has a movement

    disorder resulting from disease in the

    basal ganglia.

    The history and findings are

    characteristic of Parkinsons disease.

    Patients develop bradykinesia, rigidity,

    gait instability and tremors, usually

    beginning on one side of the body, then

    affecting the other. The lines of the face

    become smooth and the expression

    becomes fixed (masked-like facies)

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    The neurologist he consulted noticed that he has somewhat

    an immobile face and that he blinks frequently.

    Additional findings: A 4-6 cycle/second tremor of the left

    wrist and fingers, mild rigidity on passive manipulation of

    the left arm and left, and slowness of the finger movements

    of both hands.

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    Characteristics Helpful Mnemonics

    Parkinsons Disease Lewy bodies

    Depigmentation of

    substantia nigra pars

    compacta (loss of

    dopaminergic neurons)

    TRAP = Tremor (at rest

    eg pill-rolling tremor),

    cogwheel Rigidity, Akinesia,

    and Postural instability

    Huntingtons Disease Autosomal dominant

    trinucleotide repeat

    disorder

    Chorea, depression,

    progressive dementia

    Expansion of CAG.

    Caudate loses Ach and

    GABA.

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    Characteristics Mnemonics

    Hemiballismus Sudden, wild flailing of 1 arm +/- leg

    Contralateral subthalamic nucleus lesion

    (e.g. lacunar stroke in pt with

    hypertension)

    Loss of inhibition of thalamus thru globus

    pallidus

    Half ballistic (as in throwing

    a baseball)

    Chorea Sudden, jerky, purposeless movement

    Characteristic of basal ganglia lesion.

    Choreadancing (Greek)

    Think choreography

    AthetosisSlow, writhing

    movementCharacteristic of basal gangial lesion. Athetosnot fixed (Greek)Think snakelike

    Myoclonus Sudden, brief muscle contraction Jerks, hiccups

    Dystonia Sustained, involunatry muscle

    contractions

    Writers cramp

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    TREMORS

    Essential/postural tremor

    action tremor (worsens when holding posture), autosomaldominant.

    Often self medicate with alcohol (decreases tremors) Tx: Beta blockers

    Resting tremor

    Most noticeable distally

    Parkisons

    disease (pill-rolling tremor) Intention tremor

    Slow, zigzag motion when pointing toward a target

    Cerebellar dysfunction

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    APHASIAS

    Higher-order inability to speak (vs. dysarthria: motor

    inability to speak)

    Brocas

    Nonfluent aphasia with intact comprehension( to remember: Brocas Broken Boca)

    Brocas area: inferior frontal gyrus

    Wernickes

    Fluent aphasia with impaired comprehension

    ( to remember: Wernickes is Wordy but makes no sense!)

    Wernickes area: superior temporal gyrus

    Global

    BOTH affected: Nonfluent aphasia with impaired comprehension

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    A gunman shoots a 25 year-old policeman in the abdomenduring an armed robbery. The policeman is quickly transported

    to the hospital, where he is awake and alert.

    PE shows moderate blood loss from wound but stable BP and

    pulse

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    Neurologic exam:

    Weakness of R leg with decreased DTR

    No response to plantar stimulation of R foot

    Loss of position sense and vibration sense in entire R leg Loss of pain and temp sensation in L leg and L lower abdomen

    X-ray:

    Bullet lodged in lower thoracic spine

    He is taken to surgery, where the abdominal wound is explored and the

    bleeding is stopped. No major organ injury has been sustained, and noattempt is made to remove the bullet.

    Over the next several months, the patient recovers most of his strength in the

    R leg, but it is stiff when he moves.

    Examination 6 mos post-op reveals:

    increased DTRs in the R leg

    a right extensor plantar response

    diminished position sense and vibration sense in the R leg

    diminished pinprick sensation in the L leg and lower abdomen.

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    Question 1: What structures in this man spinal cord have

    been damaged to cause the neurologic abnormalities?

    Matching Type! (letters may be repeated)1. Weakness of R leg with decreasedDTR

    2. Loss of position sense and vibration

    sense in entire R leg

    3. Loss of pain and temp sensation in L

    leg and L lower abdomen

    (a) Right lateral column

    (b) Right dorsal column

    (c) Left lateral column

    (d) Left dorsal column

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    ANSWER: A. Right Lateral Column

    Right corticospinal tract

    Note that a lesion caudal/distal to the

    decussation causes signs on the ipsilateral side.

    results in UMN signs (see next slide)

    1. Weakness of R leg with decreased

    DTR

    2. Loss of position sense and vibration

    sense in entire R leg

    3. Loss of pain and temp sensation in L

    leg and L lower abdomen

    ANSWER: B. Right Dorsal Column

    Loss of position sense, vibration sense, and

    tactile discrimination on the ipsilateral side

    below the level of injury. Because of the paralysis, sensory ataxia,

    which may otherwise occur, cannot be

    demonstrated readily,

    ANSWER: A. Right Lateral ColumnRight lateral spinothalamic tract

    Loss of pain and temp on contralateral side

    beginning one or two dermatomes below the

    level of injury

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    The policeman received an

    injury to the right lateral part of

    the lower thoracic spinal cord.

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    Question 2: Is this an UMN or a LMN lesion? ANSWER: UMN

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    Question 2: What condition does the policeman have?

    (a) Syringomyelia

    (b) Amyotrophic lateral sclerosis

    (c) Brown-Sequard Syndrome

    ANSWER: C

    Lateral hemisection of the spinal cord (e.g. From a bullet or knife wound)

    Brown-Sequard. The specific effects in the patient with a chronic lesion can be

    understood by considering the fiber tracts and roots affected by the lesion

    discussed in the previous slide.

    Syringomyelia damages the anterior white commissure of the spinothalamic tract

    resulting in bilateral loss of pain and temp sensation.

    ALS: both UMN and LM signs; no sensory deficits

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