Chapter 11 - Neurosurgery Flashcards

1
Q

The timetable and mode of presentation of neurologic disease may provide the first clues as to its nature. ___ problems have sudden onset, without headache when they are ___, and with very severe headache when they are ___.

A

Vascular; occlusive; hemorrhagic

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2
Q

___ have a timetable of months and produce constant, progressive, severe headache, sometimes worse in the mornings. As ICP increases, what 2 symptoms are added?

A

Brain tumors; blurred vision and projectile vomiting

Note - if the tumor presses on a specific area of the brain, there may be functional deficits

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3
Q

___ problems have a timetable of days or weeks and often an identifiable source in the history.

A

Infectoius

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4
Q

___ problems develop rapidly (hours or days) and affect the entire CNS.

A

Metabolic

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5
Q

___ diseases usually have a timetable of years.

A

Degenerative

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6
Q

Presentation of TIA?

A

Sudden, transitory losses of neurologic function that come on without headache and resolve spontaneously leaving no neurologic sequela.

Specific symptoms depend on the area of the brain affected, which is in turn related to the vessels involved

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7
Q

Most common origin of TIA?

A

High-grade stenosis (70% or above) of the internal carotid, or ulcerated plaque, at the carotid bifurcation

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8
Q

What is the importance of TIAs and how does this affect management?

A

They are predictors of stroke. Timely elective carotid endarterectomy may prevent or minimize that possibility.

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9
Q

Work-up of suspected TIA?

A

Non-invasive Duplex studies (high-quality sonogram plus Doppler)

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10
Q

When is surgery (carotid endarterectomy) indicated for TIA?

A

If the lesions described above are found in the location that explains the neuro symptoms

Note - angioplasty and stent can be done if a filter is first deployed to prevent embolization of debris to the brain

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11
Q

Presentation of ischemic stroke?

A

Sudden onset without headache. Neuro deficits are present for a longer time, leaving permanent sequelae.

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12
Q

Ischemic strokes that have been present for longer than ___ hours are not amenable to revascularization procedures - why not?

A

3; if blood supply to the brain is suddenly increased, ischemic infarct may be complicated by a hemorrhagic infarct

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13
Q

Work-up of ischemic stroke?

A

At the first sign of a sudden-onset neuro deficit, patient is urged to report to the ER.

CT scan to rule out infarcts that are too extensive to be treated and confirm there is no hemorrhage
(Vascular work-up in the future to identify and treat lesions that might produce another stroke)

If at any time the neuro functions spontaneously return, reclassify as TIA and manage accordingly

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14
Q

Treatment of ischemic stroke?

A

IV infusion of tissue-type plasminogen activator (t-PA) - best within 90 minutes, but can be done up to 3 hours after onset of symptoms

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15
Q

Presentation of hemorrhagic stroke?

A

Uncontrolled hypertensive who complains of very severe headache of sudden onset, develops severe neuro deficits

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16
Q

Dx and Rx hemorrhagic stroke?

A

CT scan to evaluate location and extent of hemorrhage; therapy directed at control of HTN and rehabiliation efforts

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17
Q

Presentation of sub-arachnoid bleeding from intracranial aneurysms?

A

Wide spectrum of severity when it first presents. Some patients are not salvageable.

Extremely severe headache of sudden onset, like no other ever experienced before.

May be no neuro findings at all because the blood is in the subarachnoid space and there is no hematoma pressing on the brain; if not recognized, often re-present ~10 days later with another bleed

May have meningeal irritation and nuchal rigidity

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18
Q

Work-up for suspected subarachnoid hemorrhage?

A

CT scan looking for blood in the subarachnoid space

Spinal tap can identify old blood or small amounts of current blood but it is never the first test

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19
Q

Rx subarachnoid hemorrhage?

A

Arteriogram to locate the aneurysm and clip it; endovascular coiling is the radiological alternative

20
Q

Are most intracranial tumors metastatic or primary?

A

Metastatic (one of the four favorite destinations of blood-borne malignant cells -> brain, bone, liver, lung)

21
Q

Common sources of metastatic brain tumors?

A

50% - lung

Next most common are breast and melanoma

22
Q

Presentation of intracranial tumor?

A

Symptoms of space-occupying lesion (progressively increasing headache for several months, worse in the morning)
Eventual signs of increased ICP (blurred vision, papilledema, projectile vomiting)
Extreme -> bradycardia, HTN (due to Cushing reflex)
History of lung, breast, skin cancer

23
Q

About 50% of primary brain tumors in adults are ___; ___ account for about 20%.

A

Glioma; meningioma

24
Q

What is the most malignant intracranial tumor? Which are usually benign

A

Glioblastoma multiforme (type of glioma); meningioma

25
Q

Rx brain tumors?

A

Surgery, radiation, chemo for cases where the BBB has already been breached

26
Q

Dx and Rx brain tumors?

A

MRI (gives better detail than CT)

While awaiting surgical removal, treat increased ICP with high-dose steroids (dexamethasone)

27
Q

Presentation of tumors at the base of the frontal lobe?

A

Inappropriate behavior
Optic nerve atrophy on the side of the tumor
Papilledema on the other side
Ansomia

(Foster-Kennedy syndrome)

28
Q

Presentation of craniopharyngioma?

A

Youngsters who are short for their age
Bitemporal hemianopsia
Calcified lesion above the sella on CT scan

29
Q

Presentation of prolactinomas?

A

Amenorrhea and galactorrhea

30
Q

Diagnostic work-up of prolactinomas?

A

R/o pregnancy
R/o hypothyroidism
Determine Prl level
MRI of sella

31
Q

Rx prolactinomas?

A

Bromocriptine or a similar drug is used in most cases

Transnasal, trans-sphenoidal surgical removal is reserved for those who wish to get pregnant or who fail to respond to bromocriptine

32
Q

Presentation of acromegaly?

A

Huge hands, feet, tongue, and jaws

HTN, DM, sweaty hands, headache, history of wedding bands or hats that no longer fit

33
Q

Work-up for suspected acromegaly?

A

Determination of somatomedin C

Pituitary MRI

34
Q

Rx acromegaly?

A

Surgical removal preferred
Radiation is an option
Somatic changes are irreversible

35
Q

___ occurs when there is bleeding into a pituitary tumor, with subsequent destruction of the pituitary gland.

A

Pituitary apoplexy

36
Q

Presentation of pituitary apoplexy?

A

History with clues to a pituitary tumor (headache, visual loss, endocrine problems)

Severe headache followed by signs of increased compression of nearby structures by the hematoma (deterioration of remaining vision, bilateral pallor of the optic nerve), and pituitary destruction (stupor and hypotension)

37
Q

Dx/manage/Rx pituitary apoplexy?

A

Steroid replacement is urgently needed; other hormones will eventually need to be replaced

MRI or CT will show extent of problem

38
Q

Presentation of tumors of the pineal gland?

A

Loss of upper gaze, physical finding known as “sunset eyes”

Parinaud syndrome

39
Q

Brain tumors in children are usually in the ___. ___ is the most common type. ___ is the second most common type.

A

Posterior fossa; medulloblastoma; ependymoma

40
Q

Presentation of medulloblastoma?

A

Classic cerebellar symptoms (stumbling around, truncal ataxia)

41
Q

Presentation of ependymoma?

A

These may pivot on a pedicle and children assume the knee-chest position to open the flow of CSF and relieve their headache

42
Q

Presentation of brain abscess?

A

Same manifestations of brain tumors, but a shorter timetable (week or two)

Fever, usually an obvious source of nearby infection (otitis media and mastoiditis)

43
Q

Dx and Rx brain abscess?

A

CT (more expensive MRI not needed, as they have a very typical appearance on CT)

Actual resection is required

44
Q

Presentation of trigeminal neuralgia (tic douloureux)?

A

Extremely severe, sharp shooting pain “like a bolt of lightning” in the face, brought about by touching a specific area and lasting about 60 seconds

Completely normal neuro exam

Only exam finding may be an unshaven area in the face (trigger zone that the patient avoids touching)

45
Q

Dx and Rx trigeminal neuraliga?

A

MRI to r/o organic lesions

Rx with anticonvulsants often successful (notably carbamazepine). If not, radiofrequency ablation can be done. Some believe pounding from a nearby vessel may be responsible and they advocate an operation to separate them.

46
Q

Presentation of reflex sympathetic dystrophy (causalgia)?

A

Develops several months after a crushing injury

Constant, burning, agonizing pain that does not respond to the usual analgescis

Pain aggravated by the slightest stimulation to the area

Extremity is cold, cyanotic, and moist

47
Q

Dx and Rx reflex sympathetic dystrophy?

A

Successful sympathetic block is diagnostic

Surgical sympathectomy is curative