Neuro problems Flashcards

1
Q

Most common primary brain tumor in kids? 2nd?

A
  1. Astrocytoma
  2. Medulloblastoma
  3. PNET - primitive neuroectodermal tumor
  4. Ependymoma
  5. Craniopharyngeoma
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2
Q

Posterior vermis syndrome

A

unbalanced gait,
trunk dystaxia
horizontal nystagmus
papilledema

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3
Q

Hemispheric syndrome (cerebeller)

A

arm, led and gait dystaxia
w/ ipsilateral cerebellar signs
commonly: astrocyoma/abscess

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4
Q

Strabismus abnormal findings (6)

A
constant strabismus at any age
eye deviation after 4 months of age
asymmetric corneal light reflex
asymmetric intensity of red reflex
deviation on cover test
torticolis or head tilt
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5
Q

Rx of strabismus

A

Penalization therapy: cycloplegic drops to blur normal eye
Occlusion therapy: patch normal eye
prescription eyeglasses
surgery

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6
Q

Complication of strabismus

A

amblyopia

diplopia

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7
Q

Klumpke palsy in shoulder dystocia damage to…

A

C8 and T1 nerves

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8
Q

C/f of C8/T1 shoulder dystocia

A
Claw hang:
extended wrist
hyperextended MCP joints
flexed IP joints
Absent grasp reflex
Horner syndrome
Intact Moro and Biceps reflex
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9
Q

Erb duchenne palsy damage to

A

injury to 5th and 6th cervical nerves

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10
Q

Erb duchenne pasly c/f

A
Decreased moro and biceps reflexes
Wiaters tip:
extended elbow
pronated forearm
flexed wrist and fingers
Intact grasp reflex
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11
Q

IVH assoc w/

A

Prematurity

low birth weight infants

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12
Q

What causes Posterior Vermis syndrome?

A

Medulloblastoma, which effects the cerebellar vermis

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13
Q

Seizures in early morning (moaning, grunting, pooling of saliva, then spreads to generalized tonic-clonic) 3-13 years old. What are they are what is the prognosis? What does EEG show?

A

Benign rolandic epilepsy

Excellent prognosis, most resolve by themselves during adolescence. Sometimes they are treated with valproic acid or carbamazepine

EEG shows biphasic spike and wave disturbances in the mid-temporal and central regions

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14
Q

Seizures throughout the day beginning at 5-9 years old. Seizure often accompanied by automatisms. What does EEG show?

A

Absence epilepsy (no post-ictal state)

3-Hz/second spike, treated with ethosuximide.

Resolves by adolescence with cognitive impairment

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15
Q

Seizures beginning at 3-8 months of age and characterized by brief, myoclonic jerks. What is it, what causes it, how do you treat it? What does EEG show?

A

Infantile spasms

Tuberous sclerosis, PKU, HIE, IVH, meningitis, and encephalitis

Most patients will develop moderate to severe mental retardation, and treatment is ACTH, valproic acid, and vigabatrin

EEG shows hypsarrhythmia

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16
Q

12-16 years of age, seizures involve myoclonic jerks that cause the adolescent to throw objects during their morning routine. What is it, what’s the EEG finding, what’s the treatment and the prognosis?

A

Juvenile myoclonic epilepsy (also associated with generalized tonic-clonic seizures, which are of greater concern)

EEG shows 4-6 second generalized spike or polyspike and wave activity.

Treated FOR LIFE with valproic acid

17
Q

What is cerebral palsy and what are the risk factors for getting it?

A

Injury to a developing brain (static encephalopathy) that primary effects motor function. The injury that primarily effects motor often leads to other neurologic defects, like seizures, learning disabilities, retardation, visual/auditory deficits, etc.

Risk factors are: prematurity, TORCH, traumatic delivery, low Apgar at 15 minutes, HIE, IVH, and kernicterus

18
Q

Name of the 4 types of CP

A
  1. Spastic diplegia - spasticity of lower extremities; typically arising from ischemia to zone around ventricles (which results in periventricular leukomalacia)
  2. Spastic hemiplegia - unilateral spasticity (upper limb usually effected more than lower limb); often caused by perinatal vascular insults, postnatal trauma, and CNS malformations
  3. Spastic quadriplegia - motor weakness of head, neck, and all 4 limbs. Often associated with seizures, scoliosis, GERD, and speech problems
  4. Extrapyramidal - problems controling face, neck, trunk, and limbs, but no spasticity (very hypotonic). This usually occurs in full-term infants that experience HIE or kernicterus
19
Q

What should you expect if a patient has a viral illness followed by the abrupt onset of weakness and sensory disturbances in the lower extremities.

A

Transverse myelitis (notice that it follows a viral illness and has sensory disturbances, the two things that differentiate it from Guillain-Barre)

Spontaneous recovery (although not always full recovery) in weeks or months

20
Q

What is pseudotumor cerebri? What causes it?

A

Increased ICP with a normal CSF cell count, anatomy, position, and absence of brain tumor.

Usually idiopathic, but can be caused by drugs, endocrine disorders, and thrombosis of venous sinsuses

Usually occurs in obese, adolescent females

21
Q

What condition is often mistaken as “fetal hiccups?”

A

Pyridoxine dependency - leads to generalized tonic clonic seizures soon after birth, and treatment is immediate Vit. B6

22
Q

10-20 seizures per day, starting around postnatal day 3 and usually self-resolving

A

Benign familial neonatal seizures

23
Q

What is adrenoleukodystrophy? How does it present?

A

It is a progressive demyelination of the CNS combined with adrenal cortical failure (sad)

  1. 5-10 years old, child has altered behavior
  2. Poor school performance
  3. Gait/coordination disturbances, loss of vision/hearing
  4. Seizures and a vegetative state

Physical exam will show hyperpigmentation and hyperreflexia

24
Q

If a 1-3 year old patient presents with episodes of ataxia/vertigo associated with rapid eye movements and horizontal nystagmus, what do they most likely have?

A

Benign paroxysmal vertigo

25
Q

Differentiate between partial, generalized, simple, and complex seizures

A

Partial - focal area of the brain
Generalized - whole brain
Simple - no loss of consciousness
Complex - loss of consciousness, aura, automatisms

26
Q

What type of seizure most likely occurred if it was unobserved, but the patient wet themselves or bit their tongue?

A

Partial with secondary generalization