24 September 2009

Facial Nerve Paralysis



Facial Nerve Paralysis
By: Vanessa S. Rothholtz, M.D., M.Sc.
UCI Department of Otolaryngology - Head and Neck Surgery


Chief Complaint
My Starbucks caramel macchiatto dribbled down my chin this morning, and it ruined my white coat. Now my face isn’t working. Do I need a face lift?
History
* Unilateral left-sided otalgia (TMJ)
* Fever, chills
* Headache
* Generalized fatigue
* Conjunctivitis two weeks ago (resolved with antibiotics)
* “My eczema acted up again last week, but it looked a little different.”
* Travel – Sonoma County for a friend’s wedding a last month

Physical
* Eyes: Left eye with injected conjunctiva, pupils equal and reactive
* Ears: EAC patent, TM c/m/i
* Nares: Patent, clear
* OC/OP: Dentition intact, tongue midline / mobile, No tonsillar hypertrophy
* Face:
o Normal tone and symmetry at rest
o Obvious facial asymmetry with effort
o No perceptible forehead movement
o Incomplete eye closure
o Asymmetrical motion of mouth with maximal effort

What grade of paralysis is this based on the House-Brackmann facial nerve grading scale?

House-Brackmann Facial Nerve Grading Scale

I Normal
II Normal tone and symmetry at rest

Slight weakness on close inspection

Good to moderate movement of forehead

Complete eye closure with minimum effort

Slight asymmetry of mouth with movement

III Normal tone and symmetry at rest

Obvious but not disfiguring facial asymmetry

Synkinesis may be noticeable but not severe

+/- hemifacial spasm or contracture

Slight to moderate movement of forehead

Complete eye closure with effort

Slight weakness of mouth with maximum effort


IV Normal tone and symmetry at rest

Asymmetry is disfiguring or results in obvious facial weakness

No perceptible forehead movement

Incomplete eye closure

Asymmetrical motion of mouth with maximum effort

V Asymmetrical facial appearance at rest

Slight, barely noticeable movement

No forehead movement

Incomplete eye closure

Asymmetrical motion of mouth with maximum effort

Differential Diagnosis
V Anomalous sigmoid sinus, benign intracranial hypertension, intratemporal aneurysm of internal carotid artery, embolization for epistaxis (external carotid artery branches)

I Malignant otitis externa, otitis media, cholesteatoma, mastoiditis, meningitis, parotitis, chicken pox, Ramsay Hunt syndrome, encephalitis, poliomyelitis (type I), mumps, mononucleosis, leprosy, HIV/AIDS, influenza, Coxsackie virus, malaria, syphilis, scleroma, TB, botulism, mucormycosis, Lyme disease

T Cortical injuries, basilar skull fractures, brainstem injuries, penetrating injury to middle ear, facial injuries, altitude paralysis (barotrauma), SCUBA diving (barotrauma)

A Temporal arteritis, periarteritis nodosa, Multiple sclerosis, myasthenia gravis, sarcoidosis, Wegener granulomatosis, eosinophilic granloma

M Paget disease, osteopetrosis, diabetes mellitus, hyperthyroidism, pregnancy, alcoholic neuropathy, bulbopontine paralysis, oculopharyngeal muscular dystrophy

I Bell palsy, Melkersson-Rosenthal syndrome (recurrent facial palsy, furrowed tongue), hereditary hypertrophic neuropathy, (Charcot-Marietooth disease, Dejerine-Scottis disease), Landry-Guillain-Barre syndrome, Sarcoidosis, Kawasaki disease, surgery, embolization

N Acoustic neuroma, glomus jugulare tumor, leukemia, meningioma, hemangioblastoma, hemangioma, pontine glioma, sarcoma, hydradenoma, gacial nerve neuroma, teratoma, fibrous dysplasia, von Recklinghausen’s disease, carcinomatous encephalitis, cholesterol granuloma, carcinoma (invasive or metastatic)

C Molding, forceps delivery, myotoic dystrophy, Moebius syndrome

D Vaccine for rabies, Antitetanus serum, mandibular block anesthesia

Course of the Facial Nerve
* Intracranial – Arises at the pontomedullary junction and courses with CNVIII to the internal acoustic meatus - 12mm
* Meatal – Anterior to the superior vestibular nerve and superior to the cochlear nerve – 10mm
* Intratemporal –
o Labyrinthe segment
+ Passes through narrowest part of fallopian canal - 12mm
+ Narrowest part of facial nerve. The most susceptible to compression secondary to edema.
o Tympanic segment
+ From geniculate ganglion to pyramidal turn – 11mm
o Mastoid segment
+ Exits the stylomastoid foramen – 13mm
* Extracranial – From stylomastoid foramen to pes anserinus
The longest segment of the facial nerve is:

A. Vertical of mastoid portion

B. Cisternal portion

C. Tympanic portion

D. Portion in the IAC


Blood supply to facial nerve – clinical relevance
* Courses between the epineurium and periosteum – making the blood supply at risk when mobilizing at the first genu
* Extrinsic
o Stylomastoid artery (branch of the postauricular artery of external carotid artery)
o Greater petrosal artery (branch of middle meningeal artery)
o Internal auditory artery (branch of the AICA)
* Labyrinthe segment - lacks anastomosing arterial cascades thereby making the area vulnerable to ischemia
Work Up

* Basic labs, thyroid function panel, Lyme titers ELISA for antibodies
* Audiogram
* Stapedial reflex
* EKG
* MRI with gadolinium / CT
* Nerve Excitability Test, Maximal Stimulation Test, Electroneuronography (EnoG) - Useful 72 hours post-injury

Topognostic Testing
* Schirmer test for lacrimation
* Stapedial reflex test (stapedial branch)
* Taste testing (chorda tympani nerve)
* Salivary flow rates and pH (chorda tympani)
Schirmer Test
* Greater superficial petrosal nerve
* Filter paper is placed in the lower conjunctival fornix bilaterally
* 3- 5 minutes
* Value of 25% or less on the involved side or total lacrimation less than 25 mm is considered abnormal.
Stapedial Reflex
* Stapedius branch of the facial nerve
* Most objective and reproducible
* A loud tone is presented to either the ipsilateral or contralateral ear  evokes a reflex movement of the stapedius muscle  changes the tension on the TM (which must be intact for a valid test) resulting in a change in the impedance of the ossicular chain
* If intact stapedial reflex, complete recovery can be expected to begin within six weeks
* Absence of the stapedial reflex during the first two weeks in Bell’s Palsy is common


Taste Testing
* Chorda tympani
* Extremely subjective
* Papillae generally disappear within 10 days post injury - middle 1/3 of the tongue is most indicative, because the anterior 1/3 may receive bilateral input.

Salivary flow rates
* Chorda tympani
* Cannulation of Wharton's ducts bilaterally
* 5 minute measurement of output
* Significant if 25% reduction in flow of the involved side as compared to the normal side
* Salivary pH Flow Rate
Nerve Excitability Test (NET)
* Most predictive prognostic factor for recovery of facial nerve function*
* Hilger nerve stimulator over stylomastoid foramen
* Reflects elevated thresholds for neuromuscular stimulation due to degeneration / disruption of axons (comparison to contralateral side)
* Difference > 2.5 milliamps - poor prognosis

Nerve Excitability Test (NET)
* Benefits:
o Easy to perform
o More comfortable for patient
* Drawbacks
o Subjectivity (relies on operator’s visual detection of response)
o May exclude smaller fibers (current thresholds are likely to selectively activate larger fibers with lower thresholds and not those smaller fivers closer to stimulating electrode)

Maximal Stimulation Test (MST)
* Electrical impulse administered to saturate the nerve with current and to compare it to contralateral side
* Test is repeated periodically until definitive response
* Response
o Equivalent to contralateral side
o Minimally diminished (50%)
o Markedly diminished (< 25% of normal)
o Absent
* Symmetric response within first ten days – complete recovery in > 90%
* No response within first ten days – incomplete recovery with significant sequelae
* Superior to NET - test becomes abnormal sooner, but drawback is subjectivity
Evoked electromyography (EEMG) or Electroneuronography (EnoG)
* Records compound muscle action potential (CMAP) with surface electrodes placed transcutaneously in the nasolabial fold (response) and stylomastoid foramen (stimulus)
* Waveform responses are analyzed to compare peak-to-peak amplit`udes between normal and uninvolved sides where the peak amplitude is proportional to the number of intact axons
* Most reliable in first 2-3 weeks post event (as neuropraxic fibers recover or regenerate, they discharge asynchronously and the response is subsequently diminished)
* Response < 10% of normal in first 3 weeks – poor prognosis
* Response > 90% of normal within 3 weeks of onset – 80-100% probability of recovery
* Testing every other day
* Advantages: Reliable
* Disadvantages:
o Uncomfortable
o Cost
o Test-retest variability due to position of electrodes
Electromyography (EMG)
* Measures post-synaptic membrane di/triphasic (polyphasic) potentials with voluntary muscle contraction that are present 6-12 weeks prior to visible return of function
* Assesses reinnervation potential of muscles two weeks after onset
* Limited value early in evaluation because fibrillation potentials indicating axonal degeneration do not appear until 10 – 14 days post onset
* Detection of motor units in 2 of 3 muscle groups – 87% satisfactory outcome
* Detection of motor units in 1 muscle group – 11% satisfactory
More Methods
* Antidromic (retrograde) Conduction – F-waves represent activated motor neurons in facial muscles.
* Transcranial magnetic stimulation – Enables central activation via a transcranial application of induce current via an electromagnetic coil
* Trigeminofacial Reflex – Records action potentials reflexively generated in the orbicularis oculi muscle in response to an electrical stimulus applied to V1
Lyme Disease - Borrelia Burgdorferi

* Ten percent of patients have facial nerve paralysis after 1-4 weeks incubation period
* ELISA to search for IgG and IgM antibodies
* Facial paralysis resolves in 6 to 12 months
* Treatment
o Early antibiotics
# Reduce symptoms
# Event long-term sequelae
o Children - IV penicillin, ceftriaxone or cefotaxime
o Adults - tetracycline
o Muscular therapy
Bell’s Palsy
* 60-70% cases
* Pathophysiology – Impaired “axoplasmic” flow from edema of facial nerve within fallopian canal
* Rapid onset and evolution < 48 hours
* May be associated with acute neuropathies of cranial nerves V- X
* Pain or numbness affecting ear, mid-face, tongue and taste disturbances
* Recurrences are more likely (2.5x) in patients with family history, immunodeficiency or diabetes
Bell’s Palsy Treatment
* Oral antivirals - Acyclovir - 10mg/kg (500mg) q8hrs x 7 days
* Corticosteroid taper 1mg / kg / day for 10 days
* Eye protection - lacrilube
* Follow progression with serial exams
* Facial nerve decompression
+ Progression to > 90% degeneration on ENOG
+ Performed before irreversible injury to the endoneural tubules occurs (two weeks), will allow for axonal regeneration to occur
Treatment of Bell’s Palsy with Steroids: A controversial closer look
* Steroids may have the following effects:
o Reduce risk of denervation
o Preventing / lessening synkinesis
o Preventing progression to complete paralysis
o Hastening recovery
* Controversy:

Ramsay Hunt Syndrome
Herpes Zoster Oticus (Ramsay Hunt syndrome)
* 10-15% of acute facial palsy cases
* Lesions may involve the external ear, the skin of EAC or soft palate
* Associated symptoms – hearing loss, dysacusis and vertigo
* Additional involvement of CN V, IX and X and cervical branches 2, 3 and 4
* Pathogenesis – Neural injury due to edema at point between the meatal foramen and the geniculate fossa in the labyrinthe segment
Acute Otitis Media
* History and physical exam make the diagnosis
* Palsy is progressive over 2 to 3 day period
* Infectious agent – Staphylococcus non-aureus, Propionobacterium
* CT temporal bone
* Treatment
o Myringotomy
o Otic antibiotic drops containing topical steroids
o IV antibiotics and steroids
o If not improved… mastoidectomy
Möbius Syndrome
* Most frequently sporadic
* Congenital facial weakness with impairment of ocular abduction
* Dysfunction of other cranial nerves – III, IV, IX, X, XII
* Skeletal abnormalities (orofacial, limb malformations)
* Pathogenesis – Genetic cause vs. Ischemic cause
Melkersson-Roenthal syndrome
* Triad
* Lips become chapped, fissured and red-brown in appearance
* Biopies identify granulomatous changes
* Facial nerve decompression may be indicated if facial paralysis is severe and recurrent
Neoplastic

* About 5% of cases of facial nerve paralysis are caused by tumors
* Characteristics of facial nerve palsy
+ Slow developing
+ Additional cranial nerve deficits
+ Recurrent ipsilateral involvement
+ Adenopathy
+ Palpable neck or parotid mass
* Most common benign tumor - facial nerve schwanomma
* Most common malignant tumors - mucoepidermoid carcinoma and adenoid cystic carcinoma of the parotid gland.

Temporal Bone Fractures
* Longitudinal fractures
o 80% incidence but 10-20% with facial nerve injury
* Transverse fractures
o 20% incidence, but 50% with facial nerve injury
* Most common site of fracture
o Perigeniculate region
* Penetrating injury to extratemporal facial nerve branches
* Injuries medial to a line perpendicular to the lateral canthus do not need to be explored because they recover spontaneously (draw please)
* Immediate paralysis after injury lateral to this line needs to be explored and repaired with an end-to-end anastomosis 48-72 hours after the initial injury
Sunderland Nerve Injury Classification
* I Neuropraxia
o Conduction block from compression and loss of axonic flow
o Complete recovery
* II Axonotmesis
o Axon disrupted but endoneurium preserved
o Wallerian degeneration occurs distal to site of injury
o Complete recovery
* III Neurotmesis
o Complete disruption of axon including its surrounding myelin and endoneurium
o Wallerian degeneration
o Unpredictable outcome – High risk for synkinesis
* IV Complete disruption of perineurium
* V Complete disruption of epineurium
o Risk of a neuroma from nerve sprouts outside of nerve sheath

A patient with facial nerve injury following a gunshot wound to the temporal bone typically presents with which of the following symptoms?

A. Midface branch paralysis

B. Complete facial paralysis

C. Forehead paralysis

D. Partial weakness of the facial nerve

What if the facial paralysis doesn’t resolve?
* End-to-End Anastomosis
* Cable Nerve Graft
* Hypoglossa-Facial Nerve Anastomosis (Crossover or Jump Graft)
* Muscle transposition (Gracilis)
* Static Suspension (Gortex, Threads)

Complications

* Keratitis
* Emotional/Social Issues
* Synkinesis

Facial Nerve Paralysis.ppt

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Cranial Nerve Diseases



Cranial Nerve Diseases

Cranial Nerve Disorders??
Types of Cranial Diseases
* Bell’s Palsy
* Trigeminal Neuralgia
* Conjugate Gaze Palsies
* Glossopharyngeal Neuralgia
* Hemifacial Spasm
* Hypoglossal Nerve Disorder
* Internuclear Ophthalmoplegia
* Palsies of cranial nerve that controls eye movements
* Acoustic Neuroma
* Facial Nerve
* Meniere’ Disease
* Vertigo and Dizziness
Bell Palsy
WHAT IS BELL’S PALSY?
Causes Of Bell’s Palsy
Prevalence of Bell’s Palsy
Symptoms of Bell’s Palsy
--Symptoms usually start suddenly, and range from mild to severe. They may include:

* Twitching in face
* Weakness in face
* Face feels stiff or pulled to one side
* Droopy eyelid or corner of mouth
* Drooling due to inability to control facial muscles
* Facial Paralysis of one side of the face, makes it hard to close one eye
* Change in facial expression (for example, grimacing)
* Dry eye or mouth
* Loss of sense of taste
* Difficulty with eating and drinking
* Pain behind or in front of the ear, may occur 1-2 days before muscle weakness
* Sensitivity to sound (hyperacusis) on the side of the face affected
* Headache
--These symptoms of Bell's palsy usually begin suddenly and reach their peak within 48 hours

Treatment for Bell’s palsy
* SAD NEWS!! There is no cure or normal course of treatment for Bell's palsy. The most important factor in treatment is to remove the source of the nerve damage. Some cases are gentle and do not require treatment since the symptoms usually drop on their own within 2 weeks. For some patients, treatment may include medications such as acyclovir -- used to fight viral infections -- combined with an anti-inflammatory drug such as the steroid prednisone -- used to reduce inflammation and swelling. Medications such as aspirin, acetaminophen, or ibuprofen may relieve pain, but because of possible drug interactions, patients should always talk to their doctors before taking any medications. There is a decompression surgery for Bell's palsy -- to relieve pressure on the nerve, but it is controversial and is rarely suggested.
* GOOD NEWS!! In general, the prognosis (forecast) for individuals with Bell's palsy is very good. The degree of nerve damage determines the degree of recovery. With or without treatment, most individuals begin to heal within 2 weeks after the early onset of symptoms and recuperate entirely within 3 to 6 months.

Prevention for Bell’s Palsy
* Taking Care of Yourself!!
* Use of safety measures may reduce the incidence of head injury.
* AVOID HITTING YOUR HEAD ON THE WALL !!
* Many of the other factors associated with this disorder are not readily preventable.


FAQs on Bell’s Palsy

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Multiple Sclerosis -Diagnostic Issues



Multiple Sclerosis -Diagnostic Issues
By:Christopher Bourque

* Manifestations due to CNS
o Slowing or failure of transmission
+ Inflammatory demyelination
+ Axonal damage
o Mostly damage of white matter tracts
+ Optic neuritis, weakness, sensory loss, ataxia nystagmus, bladder dysfunction, cognitive impairment
* Diagnosis based on clinical and laboratory evidence of
+ Dissemination in time
+ Dissemination in space
Patterns of MS
* Relapsing - remitting
o Attacks with complete/incomplete recovery
o Stable between attacks
* Secondary - progressive
o Initially relapsing-remitting
o Then progression +/- attacks
* Progressive - relapsing
o Initial gradual detioriation
o Subsequent episodes
* Primary progressive
o Gradual decline
o No attacks


Schumacher Clinical Criteria MS Diagnosis 1965
* Age (onset 10-50 years)
* CNS white matter disease
* Lesions disseminated in time and space
* Objective abnormalities on exam
* Consistent time course
o Attacks lasting > 24 hrs., spaced at least 1 month apart
o Slow or stepwise progression for > 6 months
* No better explanation
* Diagnosis by experienced clinician

Poser Criteria for the Diagnosis of MS 1983
* Widely used for last 20 years
* Definite or probable
* Laboratory supported MS
* Replaced by McDonald criteria 2001
o Technical advances enable quicker dx.
o Controversial
Additional Requirements to Make Diagnosis
Objective Lesions
Clinical (attacks)
McDonald Criteria
Positive CSFand
Dissemination in space by MRI evidence of 9 or more T2 brain lesions or 2 or more cord lesions or 4-8 brain and 1 cord lesion or positive VEP with 4-8 MRI lesions or positive VEP with less than 4 brain lesions plus 1 cord lesion and Dissemination in time by MRI or continued progression for 1 year

Clinical Manifestations
* Demographic
o Female
+ Women make up to 70%-75% MS patients
o Young age
+ Onset before age 16: 5% of cases
+ Peak onset post puberty, early 20’s
# Relapsing MS 28-30 years
* Symptoms
o Recent onset
o Frequently progressive
+ Coming on over 1-several days
+ Very acute symptoms possible
The MS Event
* Attack/relapse/exacerbation
o Acute episode of CNS dysfunction
o Lasting at least 24 hours
o In absence of fever or metabolic derangement
o All events within 30 days are unitary

MS Symptoms
* Motor
o Weakness, spasticity, ataxia
o Rarely radicular
+ lesion ant. horn, root entry zone
+ painful
+ atrophy
* Somatosensory
o 1st sx. in 43% patients
+ Includes visual
o Any anatomic distribution
o Any combination
+ Loss pain, temp, light touch, vbn, position
o Positive sx. common
+ Paresthesiae, hyperpathia, allodynia, dysesthesias
Nonspecific Associated Features That Suggest MS
* Excessive unexplained fatigue
* Temperature sensitivity
o Hot, humid weather
* Relatively recent symptoms
* History of Lhermitte’s sign
* History of bandlike sensation around the waist
* Uhthoff’s phenomenon
o eg, blurry vision with exercise or heat exposure * Fatigue
o One of the most important causes of disability
o Several sources
+ Handicap fatigue
# Increased effort to perform routine tasks
+ Secondary fatigue
# Depression, sleep disturbances, medication side-effects, other conditions
+ Systemic fatigue
# Chronic lack of energy, tirdness, malaise
# Etiology unknown

* Cognitive Disturbances
o Common, frequently overlooked
+ Estimated 50-75%
o Most common
+ Impaired attention, slow info processing, short term memory loss, reduced visuospatial skills, impaired executive function
o Impaired driving skills
o Important impact QoL, ADL
o Can occur independent
+ of disease course
+ other manifestations
MRI in MS
* Brain lesions
o Character
o Location
Evoked Potentials
* Visual evoked potentials
Principal Differential Diagnosis of Multiple Sclerosis

* Infection
* Inflammatory
* Metabolic
* Neoplastic
* Spine disease
Cerebrospinal Fluid
* Useful, not diagnostic
o Other conditions
+ Chronic CNS infections, viral syndromes, neuropathies
* Immunoglobulin abnormalities
o Production of immunoglobulin
# By plasma or B cells in CNS
+ Oligoclonal bands of immunoglobulin (IgG) (OCB)
# In CSF, not serum
# Isoelectric focusing technique
+ Elevated IgG index
# Ratio of IgG/protein in serum and CSF
# index = (csf IgG/csf albumin)
(serum IgG/serum albumin)

* First event - chance of progression to MS
o In 3 years
+ OCB +ve: 25%
+ OCB -ve: 9%
* CIS:clinically isolated syndrome
o 62.5% cases +ve OCB
* Clinically definite MS
o 90% +OCB
MRI in MS

* Spinal cord lesions
o Character
+ Asymptomatic lesions
+ Focal T2/proton density hyperintense lesions
+ Diffuse proton density abnormalities
+ Atrophy
+ Asymmetric involvement
# Multiple scattered lesions
+ Edema with acute plaques
# Often enhancing
o Location
+ Cervical and thoracic
# Especially midcervical
+ Peripheral
+ Less than 2 vertebral segments
+ Less than 50% cross-sectional area
+ Lateral, dorsal cord
Paroxysmal Symptoms in MS
* Trigeminal neuralgia (and others)
* Tonic “seizures”
* Paroxysmal dysarthria
* Hemifacial spasm
* Paroxysmal itching
* Abrupt loss of muscle tone
* Paroxysmal aphasia
* Paroxysmal kinesogenic choreoathetosis
* Lhermitte’s sign
* Visual symptoms, afferent
o Almost any pattern, related to location
o Optic neuritis
+ Central scotoma
# Mild: color desaturation
# Severe: blindness
* Vast majority have excellent return by 6 months
+ Frequent pain
# Worse on eye movement
Optic Neuritis Risk of Subsequent MS
* Other Brain Stem Structures
o Facial weakness
o Vertigo
o Loss of hearing, taste
o Dysarthria, dysphagia
+ Bulbar muscles
# Weakness, ataxia, spasticity
* Psychiatric Disturbances
o Depression
o Emotional incontinence
* Bladder dysfunction; the importance of urodynamic studies
o Failure to store: detruser hyperactivity
+ Urgency, frequency, nocturia
o Failure to empty
+ Detruser-sphincter dyssynergia
+ Poor detruser contraction
# Hesitancy, increased residual vol., retention
o Both
+ Combined
# detruser hyperactivity
# detruser-sphincter dyssynergia
o Incontinence
+ Detruser hyperactivity or
+ Overflow
+ Symptoms may not be accurate indicator of urodynamic pathology
* Bowel dysfunction
* Sexual dysfunction
o Erectile dysfunction
o Women: loss of libido, anorgasmia
o Both sexes
+ Loss of perineal sensation
+ Neuropathic pain
+ Spasticity
+ Incontinence
+ Depression, fatigue

Pain Syndromes in MS
* Primary pain
o Neuralgic
+ Trigeminal neuralgia
+ Other neuralgias
o Dysesthetic pain
+ Most often burning (legs)
+ Other dysesthesias
o Radicular pain
o Tonic seizures
o Spasticity
+ Flexor spasms
+ Extensor spasms
* Secondary pain
o Low back pain
o Osteoporosis with fractures
Neurologic Syndromes Likely for MS
* Optic neuritis
+ Unilateral eye involvement
+ Retrobulbar rather than papillitis
+ Eye pain
+ Partial vision loss, with at least some recovery
+ No retinal exudates, disc hemorrhages, macular star
o 10 years follow-up: 38% develop MS
+ MRI other lesions: risk 56%
+ MRI normal: risk 22%
o 20 years follow-up: 70% develop MS
* Transverse Myelitis
+ Incomplete
+ Sensory > motor
+ Associated
# Lhermitte’s sign
# Bandlike abdominal or chest pressure
* Internuclear Ophthalmoplegia
* Trigeminal Neuralgia
* Hemifacial Spasm
* Paroxysmal symptoms
+ Last seconds to minutes
+ Occur multiple times daily
o Tonic spasms
o Dysarthria, ataxia
o Hemiparesis, hypesthesia
Clues to a Misdiagnosis; MS
o Examination
+ Prominent
# fever, headache, uveitis, pain
+ Abrupt
# hemiparesis, hearing loss
+ No
# optic nerve/ocular involvement
# bowel/bladder involvement
+ Progressive myelopathy
# Without bowel/bladder involvement
+ Impaired level of consciousness
+ Nonscotomatous visual field defects
+ Grey matter features
# Early dementia, aphasia
# Fasciculations
# Extrapyramidal features
o MRI
+ Brain
# Normal
# Small lesions < 3 mm.
# Subcortical location (internal capsule)
# Prominent infratentorial involvement
# Prominent grey matter involvement (basal ganglia)
# Symmetric, confluent hemispheric white matter involvement
# Hydrocephalus
# Severe cerebellar/brain stem atrophy
# No callosal/periventricular lesions
* Manifestations due to CNS
o Slowing or failure of transmission
o Mostly damage of white matter tracts
o Recent appreciation of axonal/grey matter involvement
* Diagnosis based on clinical and laboratory evidence of
o Dissemination in time
o Dissemination in space
o Recent appreciation of role of MRI in assisting diagnosis
* In-office pattern recognition
o Appropriate demographic
o Appropriate clinical event

Multiple Sclerosis Diagnostic Issues.ppt

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