Neurology Flashcards

1
Q

What are headache red flags?

A

wakens child from sleep, sudden increasing severity, change in pattern, gradually increase in severity/frequency (increased ICP)

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2
Q

Red flags on physical exam?

A

growth in head circumference (b/c sutures are open), papilledema, focal neuro deficits

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3
Q

Examples of migraine variants

A

paroxysmal torticollis, cyclic vomiting, abdominal migraine, confusional migraine, benign paroxysmal vertigo

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4
Q

Conditions to r/o w/migraine variants

A

posterior fossa pathology, epilepsy, tumors, GI d/o, urea cycle d/o, drug abuse

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5
Q

What is paroxysmal torticollis?

A

attacks of head tilt from SCM spasm, can cause vertigo and/or vomiting

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6
Q

What is benign paroxysmal vertigo?

A

attacks of vertigo w/nystagmus and vomiting followed by sleep

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7
Q

What is abdominal migraine?

A

acute, severe midline abd pain w/nausea, vomiting, anorexia, pallor lasting 1-72hrs

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8
Q

What is cyclic vomiting syndrome?

A

vomiting attacks, 1-4x’s/hr for up to 5 days not attributable to other causes

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9
Q

What is confusional migraine?

A

episodes of disorientation/combativeness, end in HA

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10
Q

What is pseudotumor cerebri (idiopathic intracranial HTN)?

A

increased ICP w/o a mass or hydrocephalus possibly resulting from impaired CSF reabsorption (similar to communicating hydrocephalus)

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11
Q

What are the risk factors for pseudotumor?

A

girls, overweight, 8-13yo, sinus thrombosis, head injury, SLE, chronic CO2 retention

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12
Q

Signs and sx’s of pseudotumor?

A

HA, papilledema, vision changes, pulsatile tinnitus, CN VI paresis (cannot abduct), vomiting, pain w/eye mov’t, increased ICP w/nml ventricle size

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13
Q

What test do you need to do to diagnose pseudotumor?

A

CT/MRI of head to r/o mass, especially BEFORE doing a LP–otherwise cause hemorrhage w/mass if you do an LP

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14
Q

How do you treat pseudotumor?

A

wt loss, diuretics, LP, glucocorticoids, lumboperitoneal shunt, optic n decompression

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15
Q

What is the definition of epilepsy?

A

Recurrent/repeat seizures w/o an identifiable cause

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16
Q

What are examples of symptomatic seizures? i.e. seizure w/a cause

A

infxn, trauma, hypoxia, malignancy, hypoglycemia, hyponatremia, hydrocephalus

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17
Q

What are EEGs used for?

A

Seizure type classification or subclinical seizure (see it on EEG but not otherwise visible)

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18
Q

What are abortive medications and their route of admin?

A

lorazepam-IV; diazepam-oral, rectal; midazolam-nasal, oral, rectal; phenobarbital, fosphenytoin, levotiracetam if benzos don’t work

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19
Q

What are characteristics of febrile seizure?

A

6mos to 5yo, MC childhood seizure, temp >38, can occur before or after fever, peaks 18-24mos, no other causes, seizure caused by pathogen NOT by the temp (other sources say caused by rapid temp rise), most are simple febrile seizures, often 1st sign of illness

20
Q

Criteria for simple febrile seizure?

A

< 30min total, generalized, no recurrence in 24 hrs, no focal features

21
Q

Criteria for complex febrile seizures?

A

> 15min and > 30min total, > 1 seizure in 24hrs, focal features, prolonged

22
Q

What is the DDx for febrile seizures?

A

chills/rigors, meningitis, encephalitis, tumor, metabolic d/o, neuro d/o (developmental delay)

23
Q

When should you consider an LP for febrile seizure?

A

less than 18mos old–think meningitis! esp if they have + PE findings.

24
Q

What is the risk of epilepsy in children with febrile seizures?

A

2% will go on to Dx of epilepsy

25
What is the risk of recurrent febrile seizures?
10% but higher if < 1yo (other sources say 30% recurrence)
26
What are infantile spasms (West syndrome)?
an epilepsy syndrome, need 1 of 3: spasms, mental retardation, abnormal EEG findings. Often 4-8mo, d/t damaged brain
27
What are the tx's for West syndrome?
ACTH, anti epileptics, ketogenic diet
28
What are s/sx's of neurofibromatosus type 1?
cafe au lait spots, Lisch nodules, freckling, neurofibromas, optic glioma, osseous lesion
29
What are s/sx's of neurofibromatosis type 2?
CN VIII tumor (acoustic neuroma), neurofibroma, meningioma, glioma, schwannoma, cataract
30
What is a hamartoma?
benign tumor/normal tissue growing in an abnormal place or abnormally rapidly, e.g. Lisch nodule
31
What are complications of neurofibromatosus?
scoliosis, HTN, learning disabilities, tumors, hypothalamus d/o
32
What are s/sx's of tuberous sclerosis?
seizures/infantile spasms, calcified tumors, mental retardation, hypopigmented skin lesions, shagreen patch (orange peel lesion), sebaceous adenomas, subungual fibroma
33
What are s/sx's of Sturge-Weber dz?
port wine stain, seizures, mental retardation, intracranial calcifications, hemiparesis, cerebral atrophy on CT
34
What is Guillain Barre syndrome?
acquired inflammatory demyelinating polyradiculoneuropathy following an infection
35
What are s/sx's of Guillain Barre syndrome?
ascending paresthesias and weakness/paralysis, decreased DTRs, ileus, bladder dysfxn, autonomic dysregulation
36
What is transverse myelitis?
inflammation of the spinal cord w/perivascular cupping (lymphocytes build up around vasculature) occuring after viral illness
37
What are s/sx's of transverse myelitis?
back pain at lesion, progressive leg weakness, areflexia, spincter dysfxn, sensory loss
38
When do most cases of infanitle botulism occur?
95% between 3wks and 6mos old
39
How do infants get botulism?
unprepared foods! spores can germinate in infants guts < 1yr old but not older than 1yo
40
What are s/sx's of infantile botulism, what is the tx?
symmetric descending paralysis, poor feeding, weak cry, ptosis, apnea--tx is supportive w/botulism IgG
41
How long do tics last in children?
1mo to 1 yr
42
What are some diagnostic criteria for Tourette's Syndrome?
tics nearly qd for > 1yr, no tic free periods > 3mos, motor and vocal tics, onset before age 18
43
What are s/sx's of spinal muscle atrophy type I (Werdnig-Hoffman dz)
hypotonia, weakness, low muscle mass, tongue fasciculations, spared EOM, die by age 2-3yo
44
The DDx for microcephaly includes:
trisomies, TORCH infxn, hypoxia, Tay Sachs, toxins, metabolic d/o
45
DDx for macrocephaly?
pseudomacrocephaly, increased ICP, megalencephaly, familial, thick skull