Lec 38 Cerebellum Clinical Correlations Flashcards

1
Q

Will a unilateral cerebellar lesion result in ipsilateral or contralateral deficit?

A

ipsilateral

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2
Q

Which outputs from cerebellum course in the superior cerebellar peduncle?

A

all outputs EXCEPT vestibular

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3
Q

What is path of non-vestibular outputs from the cerebellum?

A
  • ascend in the ipsilateral cerebellar peduncle and decussate in the midbrain
  • target red nucleus OR cerebral cortex via thalamus
  • become descending motor tracts [rubrospinal and corticospinal] which then cross again as they descend ending up back on the ipsilateral side
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4
Q

What are cardinal features of cerebellar dysfunction?

A
  • hypotonia
  • ataxia
  • dysarthria
  • tremor
  • ocular motor dysfunction
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5
Q

What are classic symptoms of cerebellar vermis syndrome?

A

mostly affect trunk

  • wide based stance and gait
  • difficulty maintaing posture/balance
  • gait ataxia
  • normal or slight arm coordination impairment
  • nystagmus, ocular dysmetria
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6
Q

What is one potential effect of cerebellar vermis syndrome due to its location?

A
  • caudal vermis is near 4th ventricle
  • large mass lesion/edema of vermis can obstruct 4th ventricle
  • -> obstructive hydrocephalus
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7
Q

What is relationship alcoholism and cerebellar vermis syndrome?

A
  • alcohol and thiamine deficiency causes major cerebellar vermis degeneration
  • can cause vermis syndrome
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8
Q

What are signs of hemispheric syndrome?

A

most affect limbs

  • poor coordination ipsilateral limb movement [most noticeably speech + finger movements]
  • impaired rapid alternating movement
  • intention tremor [when voluntary movements performed]
  • dysmetria [impaired finger-nose/heel-knee-shin tests]
  • scanning or dysarthric speech
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9
Q

What is dysmetria?

A
  • inability to stop a movement at proper place

- seen in impaired finger to nose or heel-kneel-shin tests

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10
Q

What is pancerebellar syndrome?

A
  • combination of all other syndromes

- bilateral signs involving trunk, limbs, cranial musculature

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11
Q

What are possible etiologies of pancerebellar syndrome?

A
  • usually infectious/parainfectious
  • hypoglycemia
  • paraneoplastic disorder
  • toxic-metabolic disorder
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12
Q

What types of oculomotor dysfunction in cerebellar syndromes? can they help localize area of lesion?

A

frequently nystagmus especially in midline cerebellar lesions
- cannot help localize to specific area of cerebellum

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13
Q

What kind of cerebellar syndrome should you think if you see:

  • wide based gait
  • nystagmus
  • really bad headache
A

think cerebellar vermis syndrome

headache = due to 4th ventricle compression

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14
Q

What are some possible etiologies of cerebellar vermis syndrome?

A
  • alcoholism, thiamine deficiency

- large mass, lesion, edema

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15
Q

What are some possible etiologies of cerebellar hemispheric syndrome?

A
  • infart
  • neoplasm
  • abscess
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16
Q

What kind of gait do you see in cerebellar dysfunction? mid-cerebellum vs lateral cerebellum?

A
  • ataxic gait = walk is staggering/ lurching/ wavering
  • not benefitted by pts view of his surroundings = no romberg
  • mid-cerebellum –> movement in all directions
  • lateral cerebellum –> staggering/falling toward side of lesion
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17
Q

What is position of feet in cerebellar gait?

A
  • ataxia less when pts stand on broad base [feet wide apart]
18
Q

Does coordination improve in cerebellar syndrome pts with eyes open/closed?

A
  • not improved by visual orientation
19
Q

How does cerebellar ataxia differ from posterior column disease ataxia?

A

posterior column disease = + romberg sign = ataxia made worse with eyes closed

cerebellar = negative romberg

20
Q

Where do you see cerebellar hypotonia? which type of lesions?

A
  • usually in acute cerebellar hemispheric lesions
  • less often seen in chronic lesion
  • ipsilateral to side of cerebellar lesion
  • more noticeable in upper limb
21
Q

What should you think if hypertonia in cerebllar disease?

A
  • may reflect compression of brainstem/corticospinal tract
22
Q

What do finger-nose and heel-shin tests tell you?

A
  • evaluate cerebellar dysmetria
  • if its jerky = sign of dysmetria
  • cerebllar dysmetria usually due to cerebellar hemispheric function
23
Q

What is dysdiadochokinesis?

A
  • decreased ability to perform rapidly alternating movements
24
Q

What does rapid alternating movement test tell you?

A
  • evaluate for dysdiadochokinesis
25
What is cerebellar dysarthria?
- abnormality in articulation and prosody - scanning/ slurring/ staccato/ explosive/ hesitant/ garbled speech - may be due to generalized hypotonia [disorder of muscle spindle function]
26
Are hemisphere or vermal lesions more associated with speech disorders?
hemisphere lesion
27
What is a tremor?
rhythmic, alternating, or oscillatory movement | - can be normal exaggeration of movement, primary disorder, or symptom of cerebellar disroder or parkinsons
28
What is a resting tremor? what etiology?
- tremor that is maximal at rest, decreases with activity -- usually suggests parkinsons diseases or other basal ganglia lesion
29
what is a postural tremor? what etiology acute vs gradual?
- tremor that is maximal with limb in a fixed position against gravity - gradual onset means physiologic or essential tremor - acute onset means toxic/metabolic disorder
30
What is an intention tremor? possible etiology?
- tremor that is maximal during movement toward target [like finger to nose test] - suggests cerebellar disorder OR MS, wilsons disease
31
What is a physiologic tremor?
- present normally in some people - usually very slight - predominantly postural - rapid frequency [8-13 Hz] - most visible when hands outstretched and in times of stress/anxiety -- can be suppressed by alcohol or sedatives
32
What is an essential tremor?
- benign hereditary tremor [senile tremor] - medium frequency [4-8 Hz] - minimal or absent at rest - usually bilateral, can affect hands/head/voice
33
What is asterixis?
- not a tremor - muscle tone lapses when wrist extension attempted - repetivie, nonrhythmic, non-oscillatory wrist flexion - 3-5 Hz - bilateral - sign of chronic renal or liver failure
34
What should you think if you see asterixis?
- chronic renal or liver failure | - if liver failure --> also may have hepatic encephalopathy [acute confused state]
35
What is myoclonus?
- quick movement of muscle - also can be confused with tremor - focal, segmented, or generalized - cannot be suppressed [unlike a tic]
36
What is palatal myoclonus? possible etiologies?
- involuntary rhythmic jerk of soft palate - not suppressed by sleep - pts aware of click - consider MS, lesion of central tegmental tract
37
What causes cerebellar ataxia?
insult to cerebellum and connecting paths
38
What are causes of acquired ataxias?
endocrine disorders --> hypothryoidism, hypoparathyrodism, hyoglycemia hypoxia/hyperthermia due to purkinje cell damage toxins especially alcohol cause midline atrophy, heavy metals meds: chemotherapy + antiepileptic drugs creutzfeld-jakob disease autoimmune vascular lesions in cerebellum celiac
39
What are some causes of inherited ataxias?
- friedreich ataxia | - ataxia-telangiectasia
40
What is fredreich ataxia?
- chronic slow progressive cerebellar ataxia - onset ages 2-25 - inheritance autosomal recessive - low extremity reflexes absent - ataxia due to degeneration sensory nerve tissue in spinal cord
41
What is ataxia telangiectasia?
- slow progressive ataxia - onset in infancy - inheritance autosomal recessive - pts present with ataxia + capillary dilations
42
What is creutzfeldt jakob disease?
- rapid progressive dementing illness - due to accumulation mutation prion protein - get UMN signs, ataxia - survival 7wk - 8 yrs