Unit 3 Pathophysiology - Chapter 18 Disorders of central and peripheral nervous systems and the neuromuscular junction Flashcards

1
Q

Primary brain injury

A
  • impact
  • focal or diffuses w/ open or closed-head injury
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Severity of TBI graded by

A

glascow coma scale

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Focal brain include which of the following (8)

A

1) coup - injury at site of impact (hit steering wheel)
2) contrecoup - injury frojm brain rebounding and hitting opposite side of skull (after hitting wheel, brain hits back of skull)
3) contusion - bruising of brain
4) laceration - tearing of brain tissue
5) extradural (epidural) hematoma - accumulation of blood above dura mater
6) subdural hematoma - blood between dura mater and arachnoid membrane
7) intracerebral hematoma - bleeding into the brain
8) open-head trauma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Open head injury

A
  • skull fracture
  • exposed cranial vault to environment

different kinds of skull fractures:
* compound fracture or perforated fracture (open visible fracture via observing skin)
* linear fracture: break in bone, however bone did not move
* comminuted fracture: broken in at least 2 places (car accidents for e.g); need surgery and year or longer to recover
* basilar skull fracture: substantial blunt force, break in at least one of the bones at the base of the skull (bottom)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

basilar skull fracture (in-depth)

A
  • r/t base of skull (can be multiple spots)

location of fossa w/ sx
* anterior: raccoon eyes, halo sign, partial/total loss of vision + smell, eye mvmt defects
* middle: damage to carotid A, hearing loss, loss of balance, battle sign
* posterior: cervical spine injury, vertbal a. injury, damage to lower cranial nerve

Battle signs (ecchymosis behind the ear), laceration in the ear canal, and blood or CSF in the ear canal may indicate a fracture of the skull base or of the glenoid fossa.

order – frontal bone => sphenoid bone => temporal bone (sides) => occiptal bone

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

closed head injuries

A
  • precise location w/ mild severity for most cases
  • more severity: include contusions, epidural, subdural, subarachnoid , and intracerebral hemorrhage
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Diffuse axonal injury (DAI)

A
  • d/t mechanical forces: acceleration, deceleration, and rotation that causes stretching and shearing of axons (only visible under microscope); can be mild, moderate, or severe
  • such as shaking or strong rotation of head by physical forces (e.g car crash)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Secondary neuronal injury

A
  • caused by indirect result of primary brain injury
  • includes: hypotension, hypoxia, anemia, hypoglycemia, hyperglycemia, and hypercapnia or hypocapnia (systemic)
  • cerebral contributions: inflammation, oxidative stress, alterations in the blood-brain barrier, excitotoxicity, cerebral edema, increased intracranial pressure (IICP), decreased cerebral perfusion pressure, cerebral ischemia, and brain herniation
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Complication of TBI

A
  • postconcussion syndrome:
    1) headache, dizziness, fatigue, nervousness or anxiety, irritability, insomnia, photophobia, depression, inability to concentrate, and forgetfulness, and may last for weeks to months
    2) drowsiness or confusion, nausea or vomiting, severe headache, memory deficit, seizures, drainage of CSF from the ear or nose, weakness or loss of feeling in the extremities, asymmetry of the pupils, and double vision
  • posttraumatic seizures (epilepsy):
    1) 10% of TBIs, highest amongst open brain injuries
    2) phenytoin used for moderate to severe TBI at time of injury
  • Chronic traumatic encephalopathy (CTE)
    1) dementia pugilistica before…
    2) progressive dementing disease that comes from repeated brain injury d/t sports, blast injuries as soldier, or work related head trauma (tau neurofibrillary tangles present in brain
    3) sx’s include: violent behaviors, loss of control, depression, suicide, memory loss, and cognitive change.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Spinal cord and vertebal injuries affect who most?

A
  • young men d/t rereational or travel
  • OA d/t preesxisting degenerative vertebral d/o
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Vertebral injuries include?

A
  • fractures
  • dislocations
  • compressions
  • penetrating bone

types:
1) simple - fracture of only bone
2) compressed - cause the vertebrae to collapse, making them shorter in height. This collapse can also cause pieces of bone to press on the spinal cord and nerves, decreasing the amount of blood and oxygen that gets to the spinal cord
3) comminuted - at least 2 places

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Primary spinal cord injury

A
  • damage to neural or vertebral injury d/t
    1) shearing (opposite directions when force applied)
    2) compression
    3) traction (pulling force)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Secondary spinal cord injury

A
  • d/t edema, ischemia, excitotoxicity, inflammation, oxidative damage, activation of necrotic and apoptotic cell death and beings w/ minutes of injury while continuing for weeks
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Neurogenic shock

A
  • vasogenic shock
  • occurs w/ cervical or upper thoracic cord injury above t5
  • can be seen with spinal shock
  • loss of sympathetic acitivity w/ unopposed vagal parasympathetic activity, including sx of hypotension, bradycardia, and hypothermia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Paraplegia vs quadriplegia

A
  • paralysis of lower half of body with both legs
  • involve all 4 extremities
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How does reflex activity return to those w/ acute spinal cord injury?

A

Slow
* reflex activity can return in 1-2 weeks in most people w/ this condition
* flexion reflex patterns return, first the toes then feet + legs
* eventually reflex voiding and bowel elimination appear (only when full)
* mass reflex (flexor or bending spasms w/ sweating, piloerection, automatic bladder emptying) may develop too

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Autonomic hyperreflexia (dysreflexia)

A
  • syndrome of masssive reflex sympathetic discharge d/t sinpal cord injury at t5-t6 or above and can cause life-threatening HTN; accompanied by low heart rate
  • What can trigger AD? => bladder (blocked catheter), bowel impacted (constipation), skin + pressure wound (d/t infection and fluid loss can trigger as well), fractures/dislocations, gastric ulcers, surgeries, labor + delivery

1) stimulus from below injury (distended bladder or bowel)
2) afferent stimulus
3) massive sympathetic response at injury site (release norepinephrine)
4) cause skin and abdomen to constrict raising BP
5) baroreceptors in heart/neck detect HTN, which then send signals to brain (cranial nerve IX, X)
6) cranial nerve X send signals to hear to slow down heart via parasympathetic vagus nerve (HR)
7) finally reaches spinal cord to attempt to open vessels again but d/t injury signals stop at site and only vessels above injury dilate; this is not enough to overcome the constricted vessels below injury level so BP continues to increase!

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Pathologic findings of Degenerative disk disease (DDD)

A

1) disk protrusion - occurs when the spinal discs and associated ligaments are intact, but may form an out pouching that will press on the spinal nerves. This condition causes pain in the neck, shoulder and the arms.
2) spondylosis - spinal defect or fracture of a bone structure called the pars interarticularis, which connects the facet joints of the spine.
3) subluxation - misaligned vertebrae within the spine from its normal position
4) spondylolisthesis - degeneration of vertebrae
5) spinal stenosis - narrowing of the spinal canal in the lower part of your back. Stenosis, which means narrowing, can cause pressure on your spinal cord or the nerves that go from your spinal cord to your muscles.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Low back pain

A
  • between lower rib cage and gluteal muslces; often radiating to thigh
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

cause of low back pain?

A

mainly unknown

1) disk prolapse (outer fibers of intervertebral disc are injured and soft materal, nucleus pulposus, enclosure ruptures
2) tumor
3) bursitis (small, fluid filled sacs called bursae that cushion bones, tendons, muscles near joints => inflammed) // elbows, knees [line outside of bone]
4) synovitis (inner lining of the joint [synovium] becomes inflamed)
5) DDD - cushioning in your spine beings to wear away
6) osteoporosis - bone minieral density and bone mass decreases or when quality of bone changes [l/t fracture]
7) hyperparathyrodism - too much PTH causes Ca++ to rise in blood l/t bone thinning and kidney stones (detects low calcium in system)
8) fracture
9) inflammation
10) sprain

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Causes of DDD

A
  • part of normal aging d/t continued vertical compression of spine mainly in lumbar
  • genetic + environmental factors contribute to loss of disk connective tissue
  • disks can tear + herniate => pinch nerves and spine strain
  • spondylolysis or spondylolisthesis (or both) plus degeneration of vertebrae and spinal stenosis

Spondylolysis, or spinal osteoarthritis, is a painful condition that’s caused by aging and wear-and-tear on the spine.

Spondlylolisthesis occurs when one of the vertebrae in the spine slips forward and out of place.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Spondylolysis

A

Spondylolysis is a spinal defect or fracture of a bone structure called the pars interarticularis, which connects the facet joints of the spine => deficient vertebra (spondyloisthesis) => lower back pain

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Cervical spondylolysis

A
  • facet hypertrophy (facet joints in spine become enlarged) and disk degeneration w/ narrowing in the cervical spine usually c5-c6 and c6-c7
  • causing following:
    1) radiculopathy (injury or damge to nerve roots in area where they leave the spine)
    2) myelopathy (injury in spinal caused by severe compression d/t stenosis, disc degeneration, disc herniation, autoimmune d/o, or trauma)
    3) numbness/tingling in arms
    4) occiptal headache
    5) difficulty walking
    6) altered feet sensation
    7) sphincter disturbances (bowel + bladder)
24
Q

Spinal stenosis

A

narrowing of spinal canal
* cause pressure on spinal cord
* d/t trauma or arthritis
* sx include pain, numbness, weakness in areas of affected spinal nerves

25
Q

Herniation of intervertebral disk

A
  • protrusion of part of the nucleus pulposus
  • usually L5-S1 and L4-L5
  • extruded pulpsosu compresses nerve root causing pain that radiates along sciatic nerve (runs down from back to leg)
26
Q

Most frequent occurring neurologic disorder?

A

cerbrovascular disease; cany abnormality of blood vessels of brain is referred to as cerebrovascular disease; includes
* vessel wall abnormalities
* vascular malformations
* thrombotic or embolic occlusion
* increased blood viscosity
* clotting

27
Q

Cerebrovascular disease cause?

A

1) ischemia w/ or w/o infarction
2) hemmorhage
3) most common - CVA cerebrovascular accident or stroke syndrome (w/ following risk facotrs for it)
* Poorly or uncontrolled arterial hypertension
* Smoking, which increases the risk of stroke by 50%
* Insulin resistance and diabetes mellitus
* Polycythemia and thrombocythemia
* High total cholesterol or low high-density lipoprotein (HDL) cholesterol, elevated lipoprotein-a
* Congestive heart disease and peripheral vascular disease
* Hyperhomocysteinemia
* Atrial fibrillation
* Physical inactivity
* Family history and genetics
* Sleep apnea
* Chlamydia pneumoniae infection73
* Sickle cell disease
* Postmenopausal hormone therapy
* High sodium intake, >2300 mg; low potassium intake, <4700 mg
* Obesity
* Depression

28
Q

Transient ischemic attack

A
  • transient episode of neurologic dysfuction d/t focal cerebral ischemia
  • risk of progressing to stroke
29
Q

CVA categories

A

1) ischemic
* thrombotic (blood clot develops)
* embolic (piece of clot, foreign object, or other substance becomes stuck in blood vessel)
* hypoperfusion (low blood pressure, heart failure, loss of blood volume)
2) lacunar (small vessel disease)
3) hemorrhagic strokes (blood vessel breaks and bleeds into brain (d/t aneurysm, an ateriovenous malformation (AVM), or artery wall breaking)

bonus sx of stroke:

  • Sudden numbness or weakness of the face, arm or leg (especially on one side of the body)
  • Sudden confusion, trouble speaking or understanding speech
  • Sudden trouble seeing in one or both eyes
  • Sudden trouble walking, dizziness, loss of balance or coordination
  • Sudden severe headache with no known cause
30
Q

Ischemic strokes

A
  • interruption in brain blood flow
  • core of irreversible ischemia and necrosis or infarction that appears pale (white infarct)
  • zone around infarction has reversible ischemia called ishcemic penumbra allowing for regaining of neurologic fx, especially with thrombolytic treatment
  • A leaking blood vessel can develop in the infarcted area l/t hemoorhagic transformation (red infrat) that can be exacerbated by thrombolytic therapy
  • Reperfusion injury can occur w/ ischemic stroke
31
Q

Intracerebral hemorrhagic stroke

A
  • primarily associated w/ vessel disease r/t HTN
32
Q

Subarachnoid hemorrhage

A
  • associated w/ ruptured aneurysms, arteriovenous malformations AVMs, or cavernous angioma (abnormal tangle of tightly packed, thin-walled capillaries prone to bleeding)
33
Q

Arteriovenous malformations (AVM)

A
  • tangled mass of dialted blood vessels
  • sometimes presents at birth… can exhibit delayed age of onset
  • sx include headache, dementia to seizure, intracerebral hemorrahge (ICH) or subarachnoid hemorrhage (SAH)
  • vasospasm (narrowing of arteries => can l/t blocked blood flow; can occur 2 weeks after subarachnoid hemorrhage or brain aneurysm (bulging, weakened area in blood vessel wall l/t widening or ballooning greater than 50% of vessel’s diameter)
    PLUS
    delyaed cerebral ischemia are serious complications
34
Q

Subarachnoid hemorrhage

A
  • bleed into subarachnoid space
  • associated w/ intracranial aneurysm, AVM, and HTN
  • expanding hematoma increase ICP
  • compresses brain tissue
  • reduces cerebral perfusion
  • disrupt BB barrier
  • inflammation + neuronal death
  • secondary brain injury follows => seziures and hydrocephalus
35
Q

Migraine

A
  • episodic disorder w/ headache lasting 4-72 hours
  • headache w/ and w/o aura and chronic migraine (migraines 15 days in a month for more than 3 months)
  • can be precipitated by triggering event
  • aura associated with cortical spreading depression (initiates w/ release of neurotransmitters, such as CGRP or calcitonin gene-related peptide; has a key role in migraine initiation) + inflammation + sensitization of pain receptors
  • Glutamate increased (excitatory, regulate mood) and serotonin decrease
36
Q

Cluster headaches

A
  • trigeminal autonomic cephalalgia
  • episodic, several times during a day for period of days at different times of year (men affected mostly)
  • pain uniltaeral, intense, tearing + burning
  • w/ ptosis (drooping of higher eyelid, lacrimation, eye reddening, nausea
  • trigeminal activation is unknown
  • sympathetic nervous underactive; parasympathetic overactivity with trigger events similar to migraine
  • acute and chronic forms
37
Q

chronic paraoxysmal hemicranias

A
  • cluster-type headache occurs 4-12 times per day for 1/2 hr - 3 hrs for both men and women
  • sympathetic activity different from cluster headache; relived with indomethacin (NSAID)
38
Q

Tension-type headache (TTH)

A
  • most common type of headache
  • central + peripheral pain mechanisms are associated with this condition
  • headache bilateral with sensation of tight band around head
  • last for hours or days
39
Q

CNS infection or inflammation

A
  • bacteria, virus, parasite, mycobacteria (tuberculosis)
  • resulting infection by bacteria l/t pyogenic or pus-producing condition
40
Q

Meningitis

A
  • inflammation of brain or spinal cord
  • infected pia meter and arachnoid villi and fluid of subarachnoid space
  • viral variant – belived to be limited to meninges
  • fungal and tubercular meningitis are less common (immunosuppressed indivduals are at greatest risk
41
Q

Bacterial meningitis

A
  • meningela vessels become hyperemic (higher blood flow than normal in response to something happening in your body that increases its demand for blood) and neutrophils migrate into subarachnoid space
  • causing an inflammatory reaction => exudation (oozing out) starts and increases [fluid with high protein content] => creating edema and brain injury
42
Q

Bran abscesses

A
  • extradural (outside dura)
  • subdural (between dura mater and arachnoid membrane)
  • intracerebral (entering cerebrum)
  • d/t infections from outside CNS
  • Microorganisms gain access to CNS from adjacent sites or spread along wall of vein
  • localized inflammatory process develops with exudate formation, vessel thrombosis, and leukocyte degerenation
  • **after few days of infection l/t delimited (fixed w/ boundaries) region w/ pus center + wall of granular tissue forming a capsule **

Into nearby tissues. The fluid is made of cells, proteins, and solid materials. Exudate may ooze from cuts or from areas of infection or inflammation. It is also called pus.

43
Q

Encephalitis

A
  • acute febrile illness
  • viral origin w/ nervous system involvement
  • most common - arthopod-borne viruses and herpes simplex virus
  • l/t widespread brain edema and necrosis
  • meningeal invovlement appears in all of this condition
44
Q

Common neurologic complications of AIDs

A
  • HAND or HIV-associated neurocognitive disorder (attention, concentration, and memory; loss of motivation; irritability; depression; and slowed movements)
  • HIV neuropathy (his condition occurs when tiny holes develop in the fibers of the nerves of the spinal cord)
  • HIV myelopathy (injury to spine; progressive spastic paraparesis, gait disturbance and lower extremity sensory abnormalities including vibratory sensation)
  • opportunistic infections
  • cytomegalovirus infection
  • parasitic infection
  • neoplasms
  • pathologically: diffuse CNS involvement, focal pathologic findings, and obstructive hydrocephalus
  • HARRT - prevented neurologic development
45
Q

Multiple sclerosis

A
  • chronic inflammatory disease - degeneration of CNS myelin in gene susceptible individuals
  • unkown cause; autoreactive T and B cells recognize myelin autoantigens and produce myelin-specific antibodies
  • causing inflammatory demyelination w/ loss of oligodendrocytes (myelin-forming cells; support and insualte axons in CNS)
  • also causing plauqe information l/t disrupted nerve conduction
46
Q

Different types of multiple sclerosis

A

1) relapsing-remitting: where you have relapses (symptoms getting worse) followed by recovery (that’s when it’s “remitting”). Your disability doesn’t get worse between relapses but after each relapse it can end up worse than before.

2) primary progressive: The progressive worsening of symptoms is caused by nerve damage or loss rather than the inflammation; you will not have relapses, or attacks, early in the disease course. You also will not have remissions.

3) secondary progressive: Usually with secondary progressive MS your disability or other symptoms gradually get worse. The old pattern of you getting relapses followed by you getting better usually comes to an end. Some people may still get relapses but they don’t tend to make a full recovery afterwards.
You might notice more difficulties with getting around than before, or other symptoms might get worse. Changes can happen very slowly though. It might take some time before you and your doctor are sure you have secondary progressive MS.

4) progressive-relapsing: causes steady damage to nerves when symptoms first appear and continues to cause progressive worsening.

47
Q

Guillan barre syndrome

A
  • rare demyelinating d/o d/t antibody and cell-mediated immunologic reaction directed against peripheral nerves that causes weakness or paralysis w/ irreversible effects
48
Q

Neuropathies

A
  • injury to peripheral nerves; sensory, motor, autonomic pathways
  • axon and myelin degeneration may be present

1) generalized symmetric polyneuropathies (multiple location)
2) generalized neuropathy (one nerve?)
3) focal neuroapthy vs mutlifocal neourpathies (hand, feet, arm, torso, or leg in one nerve vs both hands with varying degrees)

49
Q

Radiculopathies

A

d/o of spinal cord nerve roots
* compressed, inflamed, or torn
* most commonly affected - cervical and lumbar nerve roots

50
Q

Plexus injuries

A
  • nerve plexus (lateral to nerve roots); proximal to formation of peripheral nerves
  • caused by trauma, compression, or infiltration w/ motor and/or sensory loss, weakness, and muscle atrophy
51
Q

Botulism

A
  • poisoning by botulinum toxin released by clostridium botulinum — acts by inhibiting release of ACh at myoneural junction causing flaccid paralysis
52
Q

Mysathenia gravis

A
  • defect in nerve impulse transmission at the neuromuscular junction with these subtypes

1) generalized (weakness involving ocular muscles, variable combination of arm, legs, and respiratory muscles)
2) ocular (first muscle weakness appears in muscles of eyelids and other muscles that control mvmt of eye [extraocular muscle]
3) neonatal (transplacental transmission of materal antibodies directed against acteycholine receptor and, less so, muscle-specific kinase => impairing transmiision)

  • autoantibodies, complement deposits, and membrane attack complex destroy acetylcholine receptor (AChR) sites l/t lower transmiision of impulses causing muscle weakness, including ocular + systemic muscles [childhood + adult]
53
Q

Tumors within cranium

A
  • primary tumors arise from brain tissue and can be classified as intracerebral or extracerebral (outside cerebrum)
  • metastatic (secondary) – more common
54
Q

Primary brain tumor types

A
  • astrocytomas – occur in brain or spinal cord; begins in astrocytes that support nerve cells (most common; star shaped cells)
  • oligodendrogliomas – rare type of brain tumour developing from glial cells called oligodendrocytes [myelinating cells of CNS]
  • mixed oligoastrocytoma – affecting both oligodendrocytes and astrocytes creating mixed tumors
  • glioblastoma multiforme (grade IV astrocytoma) — fast growing and aggressive brain tumor; invades nearby brain tissue but does not spread to distant orgrams; can start from beginning or develop from lower-grade astrocytoma
  • ependymoma - begins in ependymal cells in brain or spinal cord [cells produce CSF, line the ventricles in the brain and central canal of spinal cord]
55
Q

Other CNS tumors

A

1) meningiomas (tumor of membranes that surround brain and spinal cord) dura, arach, pia
2) schwannomas (nerve sheath tumors) – tumor arises from schwann cells that protect and support nerve cells of nervous system; often benign can become cancerous though
3) neurofibromas – benign (noncancerous) tumors that grow on nerves in the body. They consist of an overgrowth of nerve tissue along with blood vessels and other types of cells and fibers. Neurofibromas can grow on nerves in the skin (cutaneous neurofibroma), under the skin (subcutaneous neurofibroma) or deeper in the body, including in the abdomen, chest and spine

56
Q

Metastatic brain tumors

A

invade brain tissue by:
1) attaching to endothelial cells of microvessels
2) use enzymes to cross BB barrier
3) extravasate (flow out from vessel) into brain parenchyma (functional tissue)

57
Q

Spinal cord tumors

A
  • intramedullary (within neural tissues) — produce dysfunction via invasion and compression
  • extramedullary (outside spinal cord) — produce dysfunction by compression of adjacent tissue

metastatic spinal cord tumors are usually:
1) carcinomas (form in epithelial tissue)
2) lymphomas (start in lymph system; tissues that store, produce, and carry WBCs, such as hodgkin lymphoma – spreads in order from one node to another)
3) myelomas (cancer of plasma cells)