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42 Cards in this Set

  • Front
  • Back
6 symptoms of LMN lesions
1. flaccid paralysis
2. atrophy
3. areflexia
4. hypotonia
5. fasiculations
6. fibrillations
Poliomyelitis
1. prototypic disease of what?
2. caused by a...
3. results in..
1. LMNs (alpha MNs in ventral horn, esp for lower limbs)
2. enterovirus
3. flaccid paralysis
3 examples of LMN diseases
1. poliomyelitis
2. Werdnig-Hoffmann disease
3. Kugelberg-Welander
2 examples of UMN lesion locations
1. cortical neurons that give rise to corticospinal and corticobulbar tracts
2. pyramidal tract lesions (corticospinal and corticobulbar tracts)
3 ipsilateral motor deficits of a lateral corticospinal tract lesion
UMN
1. spastic hemiparesis w/ mm weakness
2. hyperreflexia
3. clasp-knife spasticity
Dorsal column syndrome
1. 2 causes
2. ipsilateral senosry deficits
1. subacute combined degeneration (B12) and tabes dorsalis (neurosyphilis)
2. tactile discrimination, proprioception, vibration, asteregonosis, dystaxia, Romberg sign
Lesions to which tracts cause leg dystaxia...
1. ipsilateral
2. contralateral
3. what test is difficult to perform
1. dorsal spinocerebellar
2. ventral spinocerebellar
3. heel to shin
Lateral spinothalamic tract lesion
1. loss off..
2. on which side
3. at what level
1. pain and temp
2. contralateral (crosses in V. commissure)
3. 1 level below lesion
Herpes Zoster
1. what is it?
2. where does it occur?
3. limited to...
4. symptoms
1. viral infaction causing an acute inflammatory rxn
2. dorsal root or CN ganglia
3. one dermatome
4. pain, itching, burning
Guillan Barre (acute idiopathic polyneuritis)
1. usually follow...
2. results from...
3. causes...
4. symptoms
5. effect on CSF
1. infectious illness
2. cell-mediated immunologic rxn directed at peripheral nn.
3. mostly motor fiber demyelination and wallerian degeneration
4. ascending LMN symmptoms: weakness, flaccid paralysis, areflexia
5. increases protein, but no impact on cell count
Amyotrophic lateral sclerosis (ALS; Lou Gehrig's)
1. prototypic disease for
2. causes
1. combined UMN and LMN
2. progressive bulbar palsy/muscular atrophy (LMN) and pseudobulbar palsy/primary lateral sclerosis (UMN)
Ventral spinothalamic tract lesion
-loss of..
-which side?
-starting at what level
1. crude touch
2. contralateral
3. 3-4 levels below lesion
Epiconus syndrome
1. which segments?
2. damages...
3. causes loss of..
4. what is absent?
1. L4-S2
2. ventral horns and long tracts
3. voluntary bladder control, lower limb motor function (thigh rotation)
4. Achilles reflex
Cauda equina syndrome
1. involves which spinal roots?
2. causes...
3. may result from..
4. often produces..
1. L3-Co
2. paralytic bladder, saddle anesthesia, motor disability, and loss of Achillies reflex (conus medullaris + epiconus)
3. intervertebral disk herniation
4. severe spontaneous radicular pain
Filum terminale (tethered cord) syndrome
1. results from
2. 3 symptoms
1. thickened, shortened filum terminale adering to sacrum (puts traction on conus medullaris)
2. sphicter dysfunciton, gait disorders, feet deformities
Subacute combined degeneration
1. also known as
2. associated w/
3. affects what 3 tracts (what losses?)
4. what does it do to them?
1. Vit B12 neuropathy
2. pernicious anemia
3. dorsal columns (prop, vib); spinocerebellar (limb ataxia); corticospinal (UMN spasticity)
4. demyelinates
Friedreich hereditary ataxia
1. how do you get it?
2. similar to subacute combined degeneration how?
3. what else is involved? (symptom)
4. commonly leads to...
1. autosomal recessive inheritance
2. degenerates dorsal columns, spinocerebellar, and corticospinal tracts
3. Cerebellum/purkinje fibers (ataxia)
4. cardiomyopathy, pes cavus, kyphoscoliosis
Syringomyelia
1. destroys..
2. interrupts (symptoms)
3. what other characteristic symptom?
4. distribution of sensory loss
1. ventral commissure
2. crossing spinothalamic fibers (bilat pain and temp loss)
3. atrophy of hand muscles
4. cape-like
Multiple sclerosis
1. most common what?
2. what kind of lesions?
3. most commonly affects what segments?
1. demyelinating diseas
2. asymmetrical lesions of white matter
3. cervical segments
Charcot-Marie-Tooth
1. aka
2. most common what?
3. affects what two areas? (Symptoms)
1. peroneal muscular atrophy (stork legs)
2. inherited neuropathy
3. dorsal columns (loss of prop, vib) and ventral horns (atrophy)
Intervertebral disk herniation
1. causes what kind symptoms?
2. occurs where 90% of the time?
3. and the other 10%?
1. spinal root symptoms: parasthesia, pain, sensory loss, hyporeflexia, mm weakness
2. L4-L5 or L5-S1
3. C5-C6 or C6-C7
Cervical spondylosis w/ myelopathy
1. most common what?
2. what causes it?
3. how does it present?
1. observed myelopathy
2. calcified disk material exuded into spinal canal compressing the spinal cord
3. stiff neck, arm pain and weakness, spastic legs, dystaxia
Hypothalamospinal tract
1. results in...
2. if transected above..
1. Horner syndrom
2. T2
Dorsal horn destruction
1. symptoms
2. on which side?
3. distributed along?
1. anesthesia and areflexia
2. ipsi
3. dermatomal distribution
Complete transection
1. at C1-C3
2. C4-C5
3. below T1
4. above C5
5. four other symptoms
1. exitus lethalis
2. quadriplegia
3. paraplegia
4. loss of voluntary breathing (phrenic nucleus)
5. spastic paralysis, anesthesia, anhidrosis, loss of voluntary bladder control
Anterior/Ventral spinal artery occlusion
1. 4 tracts it destroys (symptoms?)
2. also causes...
3. usually spares...
1.V. horn (flaccid paralysis at level); corticospinal (spastic paralysis below level); spinothalamic (loss of pain and temp); spinocerebellar (cerebellar symptoms masked by paralysis)
2. bilateral horner syndrome
3. dorsal columns
Conus medullaris syndrome
1. what segments?
2. destroys...
3. causes...
4. absence of...
1. S3-Co
2. sacral parasymp nucleus
3. paretic bladder, fecal incontinence, impotence
4. lower limb muscle deficits
1. fasciculus gracilis
2. fasciculus cuneatus
3. dorsal spinocerebellar
4. lateral corticospinal
5. lateral spinothalamic
6. ventral spinocerebellar
7. ventral white commissure
8. ventral corticospinal
A. poliomyelitis
B. multiple sclerosis
C. tabes dorsalis
D. ALS (Lou Gehrig's)
E. Brown Sequard
F. ventral spinal artery occlusion
G. subacute combined degeneration (Vit B12 neuropathy)
H. syringomyelia
I. Charcot-Marie-Tooth
J. dorsal spinal artery occlusion
Medial medullary syndrome (anterior spinal a.)
1. corticospinal tract (contra hemiparesis)
2. medial lemniscus (contra loss of vib/prop)
**3. hypoglossal n. (ipsi flaccid paralysis of tongue)
Lateral medullary (PICA; Wallenburg) syndrome
1. vestibular nuclei (nystagmus, nausea, vertigo)
2. inf cerebellar peduncle (dystaxia)
3. nucleus ambiguus (larynx/pharynx paralysis; loss of gag reflex)
4. spinothalamic tract (contra body pain/temp)
5. spinal trigeminal tract (ipsi face pain/temp)
6. ipsi Horner syndrome
Medial pontine syndrome
1. results from..
2. affected structures (resultant deficits)
1. occlusion of paramedian branches of basilar artery
2.
**a)abducent nerve (ipsi LR)
b) corticobulubar tracts (contra weakness of lower face)
c) corticospinal tracts (contra hemiparesis of body)
d)middle cerebellar peduncle (ipsi ataxia)
e) medial lemniscus (contra prop/vib)
Lateral inferior pontine (AICA) syndrome
**1. facial nucleus (ipsi facial mm, taste ant 2/3)
2. cohclear nuclei (unilateral deafness)
3. vestibular nuclei (nystagmus, nausea, vertigo)
4. spinal trigmeninal tract (ipsi face pain/temp)
5. middle and inferior cp (dystaxia)
6. spinothalamic tracts (contra body pain and temp)
7. ipsi Horner syndrome
Lateral super/mid pontine syndrome (short circumferential branch or SCA)
**1. trigeminal motor and main sensory nuclei (mm. of mastication, jaw deviates to paretic side, facial hemianesthesia)
2. cerebral peduncles (ipsi dystaxia)
3. spinothalamic and trigeminothalamic tracts (pain/temp from body and face)
4. ipsi Horner syndrom
5. medial lemniscus (contra loss of prop/vib from lower extremities)
Locked in syndrome (pseudocoma)
1. what is it?
2. what does it cause?
3. how do these people communicate?
1. infarction at base of superior pons
2. infarction of corticobulbar and corticospinal tracts (quadriplegia and loss of lower cranial nerves)
3. by blinking their eyes
Dorsal midbrain (Parinaud) syndrome
1. common cause
2. affects what structures (resultant deficits)
1. pinealoma
2. superior colliculis/pretectal area (paralysis of up & down gaze, pupillary disturbances, no convergence) and cerebral aqueduct (hydrocephalus)
Paramedian midbrain (Benedikt) syndrome (paramedia branches of PCA)
**1. oculomotor nerve (ipsi eye looks down and out, ptosis, fixed dilated pupil)
2. Red nucleus (contra dystaxia w/ intention tremor)
3. Medial lemniscus (contro prop/vib)
Medial midbrain (Weber) Syndrome (PCA and circle of willis aneurisms)
1. oculomotor nerve roots (ipsi eye down and out, ptosis, fixed dilated pupil)
2. corticobulbar tracts (contra weakness of lower face, tongue, and palate-7, 9, 10)
3. contra hemiparesis of body
Acoustic Neuroma (Scwannoma)
**1. CN VIII (cochlear n = deafness; vestibular n = nystagmus, nausea, vertigo)
**2. CN VII (facial weakness)
3. spinal trigeminal tract (CN V; anesthesia of ipsi face)
Internuclear Ophthalmoplegia (INO)
1. aka
2. results from...
3. frequent sign of...
4. causes...
5. what else causes these signs?
1. medial longitudinal fasciculus (MLF) syndrome
2. lesion of MLF in medial pontine tegmentum
3. multiple sclerosis
4. MR palsy on lateral gaze and nystagmus in abducting eye w/ normal convergence
5. abducent nucleus lesion (+ LR paralysis)
Jugular Foramen (Vernet) Syndrome
Affects what three cranial nerves?
1. glossopharyngeal-CN IX (loss of afferent gag relfex, taste post 1/3)
2. vagal-CN X (laryngeal paralysis w/ dyphagia and hoarseness, paltal paralysis w/ loss of efferent gag reflex
3. accessory-CN XI (SCM and trapezius weakness w/ shoudler drop)
Subclavian Steal syndrome
1. results from...
2. what happens to blood flow?
3. what clinical signs?
1. thrombosis of L subclavian artery proximal to vertebral a.
2. blood is shunted retrograde down the vertebral a. into the L subclavian a.
3. transient weakness and claudication of left arm on exercise and vertigo/dizziness