Pestana Chap 11 - Neurosurgery Flashcards

1
Q

How does vascular neurologic disease present in terms of timetable and mode of presentation? Brain tumors? What happens if ICP increases in either of these conditions?

A

1) Vascular problems have sudden onset, without headache when they are occlusive, and with very severe headache when they are hemorrhagic
2) Brain tumors have a timetable of months, and produce constant, progressive, severe headache, sometimes worse in the mornings
3) As ICP increases, blurred vision and projectile vomiting are added

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2
Q

What happens if a brain tumor presses on an area of the brain associated with a particular function?

A

Deficits of that function may be evident

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3
Q

What is the timetable for an infectious neurological problem? What is noted in the history? What is the timetable for metabolic neurologic problems and what part of the CNS do they effect? What is the timetable for degenerative diseases?

A

1) Infectious problems have a timetable of days or weeks, and often an identifiable source of infection in the history
2) Metabolic problems develop rapidly (hours or days) and affect the entire CNS
3) Degenerative diseases usually have a timetable of years

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4
Q

What are transient ischemic attacks (TIAs)? What do the specific symptoms depend on?

A

1) TIAs are sudden, transitory losses of neurologic function that come on without headache and resolve spontaneously leaving no neurologic sequela
2) The specific symptoms depend on the area of the brain affected, which is in turn related to the vessels involved

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5
Q

What is the most common origin of a TIA?

A

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

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6
Q

What is the importance of TIAs and what can be done to prevent or minimize the possibility of this complication?

A

They are predictors of stroke, and timely elective carotid endarterectomy may prevent or minimize that possibility

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7
Q

How does the workup of TIAs begin? When is surgery indicated? When can angioplasty and stent be done?

A

1) Workup starts with noninvasive Duplex studies (high-quality sonogram plus Doppler)
2) Surgery (carotid endarterectomy) is indicated if the lesions are found in the location that explains the neurologic symptoms
3) Angioplasty and stent can be done if a filter is first deployed to prevent embolization of debris to the brain

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8
Q

How does ischemic stroke present? When is an ischemic stroke not amenable to revascularization procedures?

A

1) Ischemic stroke has sudden onset without headache, but the neurologic deficits are present for a longer time, leaving permanent sequellae
2) Ischemic strokes that have been present for longer than 3 hours

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9
Q

What causes an ischemic infarct of the brain to be complicated by a hemorrhagic infarct? What is done for the existing infarct?

A

1) If blood supply to the brain is suddenly increased
2) Vascular workup will eventually be done to identify lesions that might produce another stroke (and treat them), but for the existing infarct, assessment is by CT scan and therapy is centered on rehabilitation

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10
Q

What has become standard practice for managing a stroke? What must be done at the first sign of a sudden-onset neurological deficit? What imaging must be done and what for? What happens if at any time during this evaluation, the neurological functions spontaneously return?

A

1) Treatment of an early ongoing stroke has now become standard practice, with one or more hospitals in each major city equipped with the necessary resources and staff and designated as the places to do it
2) At the first sign of a sudden-onset neurological deficit, the patient is urged to report immediately to the emergency room
3) CT scan is done first to rule out infarcts that are too extensive to be treated, and to confirm that there is no hemorrhage
4) The case is reclassified as a TIA and manged accordingly. But if not, no time should be wasted

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11
Q

What is the treatment of an ischemic stroke?

A

Intravenous infusion of tissue-type plasminogen activator (t-PA) is best if started within 90 minutes, but it can still be done up to 3 hours after the onset of symptoms

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12
Q

In what patient is a hemorrhagic stroke most commonly seen? What is used to evaluate the hemorrhage and what is therapy directed at?

A

1) Hemorrhagic stroke is seen in the uncontrolled hypertensive who complains of very severe headache of sudden onset and goes on to develop severe neurologic deficits
2) CT scan is used to evaluate location and extent of the hemorrhage, and therapy is directed at control of the hypertension and rehabilitation efforts

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13
Q

How does a patient with subarachnoid bleeding from intracranial aneurysms typically present? Why are patients sometimes unfortunately sent home in the presence of a subarachnoid bleed? How are other patients luckily recognized as having a subarachnoid bleed?

A

1) Extremely severe headache of sudden onset, like no other ever expeirenced before (a “thunderclap,” a headache that is “sudden, severe, and singular”)
2) Because the blood is in the subarachnoid space (there is no hematoma pressing on the brain), there may be no neurologic findings at all, and the patient is sent home
3) Luckier patients may have meningeal irritation and nuchal rigidity, and be recognized

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14
Q

What happens to patients not recognized with a subarachnoid bleed who are discharged home?

A

They often return in 10 days with another bleed, perhaps this time a much worse one (the early one is referred to as the “sentinel bleed”)

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15
Q

What does workup begin with and follow with for a subarachnoid bleed?

A

CT scan looks for blood in the subarachnoid space (spinal tap can identify old blood or small amounts of current blood, but it should never be the first test; always start with the CT) and follows with arteriogram to locate the aneurysm (a little devil off the circle of Willis)

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16
Q

What are the treatments for a subarachnoid bleed?

A

1) Clipping is the surgical therapy

2) Endovascular coiling is the radiological alternative

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17
Q

Are most intracranial tumors metastatic or primary? What are the most common sites of metastasis in the body?

A

1) Metastatic

2) The brain is one of the four favorite destinations of blood-borne malignant cells-along with bone, liver, and lung

18
Q

Where do intracranial tumors usually arise from (think mets)? What are the symptoms representative of? What is a clinical history clue that the patient has an intracranial tumor?

A

1) About half come from the lung; the next more common are breast and melanoma
2) The symptoms are those of a space-occupying lesion
3) The patient has had one of the above listed tumors in the past

19
Q

About half of primary brain tumors in the adult area are what? What percentage do meningiomas account for intracranial tumors?

A

About half of primary brain tumors in the adult are gliomas; meningiomas account for 20%

20
Q

What is the most malignant intracranial tumor? Are meningiomas malignant or benign? What does the treatment for brain tumors consist of?

A

1) The most malignant intracranial tumor is glioblastoma multiforme, a type of glioma
2) Meningiomas are usually benign
3) The treatment of brain tumors is typically multimodal, including surgery, radiation, and chemotherapy for those cases where the blood brain barrier has already been breached

21
Q

How will a brain tumor present if it presses on a “silent area” of the brain?

A

1) It may offer no clue as to location
2) The only history will be progressively increasing headache for several months, worse in the mornings, and eventually accompanied by signs of increased ICP: blurred vision, papilledema, projectile vomiting-and at the extreme of the spectrum, bradycardia and hypertension (due to the Cushing reflex)

22
Q

How are brain tumors best visualized?

A

MRI gives better detail than CT and is the preferred study, although brain tumors can be visualized very well on CT scan

23
Q

How is increased ICP from a brain tumor treated while awaiting surgical removal?

A

High-dose steroids (i.e., dexamethasone [trade name Decadron])

24
Q

How can one clinically localize a brain tumor?

A

It may be possible by virtue of specific neurologic deficits or symptom patterns. For example, the motor strip and speech centers are often affected in tumors that press on the lateral side of the brain, producing symptoms on the opposite side of the body (people speak with the same side of the brain that controls their dominant hand)

25
Q

What to tumors at the base of the frontal lobe produce?

A

Inappropriate behavior, optic nerve atrophy on the side of the tumor, papilledema on the other side, and anosmia (Foster-Kennedy syndrome)

26
Q

In what patients does craniopharyngioma occur in an how does it present?

A

Craniopharyngioma occurs in youngsters who are short for their age, and they show bitermporal hemianopsia and a calcified lesion above the sella on CT scan

27
Q

What do prolactinomas cause and who do they present in?

A

Prolactinomas produce amenorrhea and galactorrhea in young women

28
Q

What does diagnostic workup of a prolactinoma include?

A

Diagnostic workup includes ruling out pregnancy (pregnancy test), ruling out hypothyroidism (TSH), determination of prolactin level, and MRI of the sella

29
Q

What is therapy for a prolactinoma?

A

1) Therapy with bromocriptine, or a similar drug, is used in most cases
2) Transnasal, trans-sphenoidal surgical removal is reserved for those who wish to get pregnant or those who fail to respond to bromocriptine

30
Q

What is acromegaly? How does it present?

A

1) Recognized by huge hands, feet, tongue, and jaws
2) Additionally, there is hypertension, diabetes, sweaty hands, headache, and a history of wedding bands or hats that no longer fit

31
Q

How does workup of acromegaly start? What are treatment options? Are the somatic changes reversible?

A

1) Workup starts with determination of somatomedin C, and pituitary MRI
2) Surgical removal is preferred (trans-nasal or trans-sphenoidal) but radiation is an option
3) The somatic changes are irreversible

32
Q

When does pituitary apoplexy occur? Why is the history important?

A

1) Pituitary apoplexy occurs when there is bleeding into a pituitary tumor, with subsequent destruction of the pituitary gland
2) The history may have clues to the long-standing presence of the pituitary tumor (headache, visual loss, endocrine problems), and the acute episode starts with a severe headache followed by signs of increased compression of nearby structures by the hematoma (deterioration of remaining vision, bilateral pallor of the optic nerves) and pituitary destruction (stupor and hypotension)

33
Q

What treatment is needed for pituitary apoplexy? What test shows the extent of the problem?

A

1) Steroid replacement is urgently needed, and eventually other hormones will need to be replaced
2) MRI or CT scan will show the extent of the problem

34
Q

What do tumors of the pineal gland cause?

A

Loss of upper gaze and the physical finding known as “sunset eyes” (Parinaud syndrome)

35
Q

Where are brain tumors in children usually found? What is the most common type, where does it arise, and what symptoms does it manifest?

A

1) Posterior fossa
2) Medulloblastoma arises in the cerebellum and gives the classic cerebellar symptoms, such as stumbling around and truncal ataxia

36
Q

What is the second most common type of brain tumor in children? How do affected children present?

A

1) Ependymoma
2) Some of those pivot on a pedicle, and affected children often assume the knee-chest position to open the flow of cerebrospinal fluid and relieve their headache

37
Q

How does a brain abscess present in comparison to a brain tumor? What do brain abscesses usually present with? What imaging is required to view them? Is surgical resection required?

A

1) Brain abscess shows many of the same manifestations of brain tumors (it is a space-occupying lesion), but a much shorter timetable (a week or two)
2) There is fever, and usually an obvious source of infection nearby, like otitis media and mastoiditis
3) They have a very typical appearance on CT, thus the more expensive MRI is not needed
4) Actual resection is required

38
Q

How does trigeminal neuralgia (tic douloureux) present? How old are patients in general and what is found on neurologic exam?

A

1) Produces 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
2) Patients are in their sixties and have a completely normal neurologic exam

39
Q

What is the only finding on physical exam found in some patients with trigeminal neuralgia?

A

Some may have an unshaven area in the face (the trigger zone, which the patient avoids touching)

40
Q

What imaging is done for patients with trigeminal neuralgia and why is it done? What is the treatment? What do some surgeons believe is the cause?

A

1) MRI is done to rule out organic lesions
2) Treatment with anticonvulsants is often successful (notably carbamazapine). If not, radiofrequency ablation can be done
3) Some surgeons believe pounding from a nearby vessel may be responsible, and they advocate an operation to separate them

41
Q

When does reflex sympathetic dystrophy (causalgia) develop and with what symptoms does it present? What is the pain aggravated by? What is characteristic of the affected extremity?

A

1) It develops several months after a crushing injury with constant, burning, agonizing pain that does not respond to the usual analgesics
2) The pain is aggravated by the slightest stimulation of the area
3) The extremity is cold, cyanotic, and moist

42
Q

What is diagnostic of reflex sympathetic dystrophy? What is the treatment?

A

1) A successful sympathetic block is diagnostic

2) Surgical sympathectomy is curative