CNS Path Flashcards

(102 cards)

1
Q

Basilar Migraine

A

Migraine w/ a characteristic aura that produces tinnitus, vertigo, ataxia, hyperacusia, diplopia

Bickerstaffs is a more serious version of this

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2
Q

Metoclopramide

A

Dopamine antagonist used as an abortive treatment for migraine’s

-Assoc. w/ Parkinsonism

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3
Q

Cluster Headaches

A

Derived from pathologic hypothalamus fnxn and presents as unilateral, stabbing headache pain that persists for 3-6 weeks and occur at the SAME TIME; must be companied by one of these

  • rhinorrhea/congestion
  • perspiration
  • miosis/ptosis
  • periorbital edema
  • restlesness

*Comination of high conc. O2 and triptans used for abortive tx; prednisone shots and verapamil used for prophylaxis

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4
Q

Tension Headaches

A

Most prevalent headache syndrome that presents as a patient w/ pressure or squeezing around the head but DOES NOT have assoc. N/V

-Pts. have these many times a day and headaches are bilateral and not aggravated by activity

Tx: Stress reduction, Cognitive/Biofeedback therapy, better sleep habits, NSAIDs, TCAs

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5
Q

IIH

A

“Idiopathic Intracranial Hypertension”

Obstructive segments in the transverse sinus =» increased arterial flow and decreased venous outflow; predominantly in obese women of child-bearing age

**Can lead to severe vision impairment/blindness if visual disturbances are left untreated

Dx: Neuroimaging and MRV; LP once confirmed there is no mass to check for increased opening pressure and relieve headache

Tx: Weight loss, bariatric surgery, acetazolamide, topiramate, ventriculoperitoneal shunt

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6
Q

Giant Cell Arteritis

A

Occurs due to patchy/segmental inflammation of the internal elastic lamina of the temporal artery; presents as a temporal headache w/ jaw claudication, vision impairment, and mild fever in a pt. >50

Dx: Will see elevated inflammatory markers, but a temporal artery biopsy is best way to diagnose

Tx: High-dose corticosteroid for many years; will produce other profound effects with time

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7
Q

Migraine

A

Begins with the excess activation of nuclei in the brainstem (possibly the raphe nuclei) and spreads peripherally to activate the trigeminal system causing chemoreceptor activation (N/V) and autonomic activation (pallor, flushing)

Presentation: Must have had 5 attacks with pulsating hemicranial headaches that worsen with exertion; must also have at least one of the following (photo/phonophobia, N/V)

*Classically will have an aura that presents as a vision/auditory loss, parasthesia, or motor loss

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8
Q

Schizophrenia onset age

A

Late adolescence-Early Adulthood

1% prevalence worldwide

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9
Q

Cotard’s Syndrome (Nihilism)

A

Delusion in which the pt. believes they are already dead

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10
Q

Capgras Syndrome

A

A known person is not recognized and the pt. believes that they have been replaced with someone else

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11
Q

Fregoli’s Syndrome

A

Persecutor of the pt. is believed to take on other identities

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12
Q

Catatonia

A

Stiffness most commonly assoc. w/ schizophrenia

Can present as waxy flexibility, catalepsy, negativism, echolalia/praxia

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13
Q

Neurological Alterations in Schizophrenia

A

Slight decrease of overall brain volume and enlarging of the ventricles;

-May also see decreased blood flow in the frontal areas, degeneration of dendritic spines in the pyramidal neurons of the PFC, and abnormal connectivity in the brain

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14
Q

Potential Complications of Schizophrenia

A

Drug abuse

Suicide (increased risk at time of diagnosis)

Depression

Violence

-Any comorbidities are also assoc. w/ higher mortality

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15
Q

Schizophreniform Disorder

A

Pt. presents w/ a schizophrenic episode that includes 1 of the following: Delusions, Hallucinations, Disorganized speech or behavior, Negative sx

-These may last for ~ 1 month but

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16
Q

Delusional Disorder

A

Pt. has not met criteria A for schizophrenia and apart from complications from their delusion, pt. is not obviously abnormal and any manic episodes have been brief

-Specify if delusions are bizarre

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17
Q

Brief Psychotic Disorder

A

Presence of Criterion A sx for at least 1 day but

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18
Q

Heroin Withdrawal Timeline

A

3-4 Hours: Anxiety, restlessness, fear of withdrawal

8-14 Hours: More anxiety, insomnia, yawning, cramps, mydriasis

1-3 Days after last dose: Tremor, muscle spasm, vomiting, HTN, chills

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19
Q

Perinatal complications of opioids

A

IAUG

Abruption

Fetal Death

Pre-term delivery

NAS

**DO NOT CAUSE BIRTH DEFECTS

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20
Q

Opioid Addiction Management in Pregnancy

A

**AVOID WITHDRAWAL; bad for baby (increased fetal movement is an indicator)

-Methadone Maintenance is STANDARD OF CARE
Day 1: 10-20 mg dose at first and smaller doses every 6 hrs
Day 2: Give entire dose once at start of day

If dosage is >DETOX

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21
Q

Advantages of Buprenorphine tx in pregnant women

A

Increased birthweight

Longer gestation

Lower incidence of NAS

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22
Q

Neonatal Abstinence Syndrome

A

More common in methadone exposed infants than heroin exposed infants (surprisingly); typically apparent within 3 days

-Baby will present w/ hyperreflexia, tremors, ***shrill cry, fever, sweating, tachypnea, yawning, poor feeding

Tx: Supportive; diazepam, chlorpromazine, methadone

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23
Q

Somatization Disorder

A

History: Multiple recurring somatic complaints that cannot be fully explained by a medical condition; presents w/ 2 GI complaints, 1 sexual complaint, and 1 neurological complaint
-Sx are legit and pts. will undergo painful procedures

PE: Lack of physical findings to support severity of sx

Lab: None

Clinical: Dramatic presentation and pt. will be well researched on conditions; seek help from multiple doctors

Management: Pt. should have only one doctor to decrease attention given to condition and should work on the pts. insight

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24
Q

Conversion Disorder

A

History: Specific stressor will cause sx that will present in a neurological fashion (weakness, paralysis, parasthesia); primary gain (psychological)

PE: Objective signs will be negative (such as loss of reflexes)

Lab: Absent findings

Clinical: Acute onset; more common in women

Management: Focus on treating the stress assoc. w/ sx

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25
Illness Anxiety Disorder
History: High anxiety w/o somatic sx; pt. has a debilitating fear of getting sick PE: None Lab: None Clinical: Can admit that their condition is not as bad as they think; probably still practice unhealthy habits Management: Problems w/ transfer and costs of procedures
26
Body Dysmorphic Disorder
History: Pt. shows excessive concern w/ a perceived deficit in their appearance; can even be completely imagined PE: none Lab: none Clinical: Deficit is primary focus of life and will cause pts. to cover it up with dress and avoid social outings; will frequently check the deficit Management: SSRIs pretty useful
27
Factitious Disorder
History: Intentional production of sx and fabrication of disorder; goal is to gain attention and pt. will undergo extensive medical procedures to do so PE: Self-inflicted; may not add up Labs: Ditto Clinical: If confronted, pt. will leave and check into another hospital; substance abuse not uncommon; intentionally gives vague answers to questions (such as MMSE) Management: Address underlying emotional problem; pts. will refuse extensive procedures
28
Malingering
History: Faking sx for secondary gain (money, avoiding prison or deployment or school) ; can have true history of other psych issues PE: Discrepancies Lab: Discrepancies Clinical: Delay in completing tests; practice caution if pt. has been referred Management: Firm confrontation; identify second gain
29
Intellectual Disability
Reduced level of intellectual functioning causing an individual who cannot adapt to the demands of their environment; global ability is the center of the diagnosis - Pt. has subpar intellect (IQ18 years, classified as dementia - Pt. typically cannot reciprocate social interaction, has limited interests, stereotyped and repetitive speech, insists on sameness, and may have "super hearing"
30
Prader-Willi Syndrome
Deletion on chromosome 15 causes an intellectual disability and compulsive eating, bad behavior, hypogonadism, irritability
31
Fragile X Syndrome
Individual has rapid, preserved speech and variable intellectual disability -Most common inherited intellectual disability and second-most common genetic behind Down's
32
Phenyketonuria (LeGrow)
Absences phenylalanine hydroxylase can cause a severe disability that, if not controlled by diet, will result in severe intellectual disability
33
Mild Intellectual Disability
IQ of 55-69, can hold a job, and function independently unless presented w/ unusual social problem -Language and social skills development are a little slower (6th grade-ish) and probably can't have deep social relationships like marriage
34
Moderate Intellectual Disability
IQ 35-50, learns basic self-care and language, usually benefit from living in a supportive, well-structured home or community -Start seeing excessive self-stimulation, self-injury, distress due to lack of social skills, decreased self-esteem, and disruptive/conduct disorders
35
Rett's Syndrome
Pt. has normal development for first 5 months than shows deceleration of head size, wringing of hands, loss of social engagement, and impairment of motor functioning Tx: Try to advance normal development, promote learning and inhibit behaviors that prevent this
36
Specific Learning Disorder
Must identify the specific area of the deficit; pt. usually will have an average IQ and present w/ frustration or distress w/ material (increased drop-out rate) - It cannot be the result of specific motor/cognitive dysfnxn, educational opportunity must be present, and deficit alone cannot account for failures in intellectual development - Manage w/ specialized instruction, modified tests, and teacher awareness
37
Persistent Motor/Vocal Tic Disorder
Have either vocal or motor tics, not both, that present every day and cause significant distress to the pt.
38
Tourette's Disorder
Presence of Motor AND Vocal tics; can be voluntarily suppressed until pt. is overwhelmed w/ anxiety and repeats the behavior; onset is usually at 7 years Tx: Tenex, clonidine, atypicals, Haldol *Can present as a "Triad" alongside ADHD and OCD; difficult to treat but should start w/ the symptoms that cause most distress to that pt.
39
Child Onset Dysfluency Disorder
Child stutters a shitload
40
Social (Pragmatic) Communication Disorder
Ben Smith without the other signs of autism
41
Speech Sound Disorder
Articulation probs in a kid
42
Pica
Pt. may present w/ complications involving GI tract and malnourishment due to the excessive consumption of nonfood items
43
Rumination Disorder
Pt. will chew, swallow, regurgitate, and eat their food again and presents w/ signs of malnourishment and failure to thrive -Often indicative of early neglect or stress in child-parent relations
44
Conduct Disorder
Persistent and repetitive behavior by a child that may be aggressive and inappropriate relative to social norms/rules; pts. have inability to feel for others and do not understand guilt Specify if child onset (
45
Oppositional Defiant Disorder
Child has angry, irritable, and argumentative mood for greater than 6 months no matter who they're around; are "little lawyers" and debate every decision made by an authority figure -Also will blame others for mistakes, can be deliberately annoying, and have difficulty with transitions Tx: Therapy, teach parents, evaluate family for dysfunctions
46
Enuresis
Voiding of urine past the age of 5; treat w/ Bell and Pad therapy or an ultrasonic bladder alarm -If that doesn't work, use desmopressin, an ADH analog that provides temporary suppression until disorder resolves
47
Encopresis
Voiding of stool; always assoc. w/ severe mental health issue; treat by therapy, using bathroom after meals, and education
48
Separation Anxiety
Child has excessive, debilitating anxiety when leaving home or parental figures; could be due to genetics, phobic parents, or fear-provoking past experience - Pts. are prone to nightmares, eager to please, and have sx secondary to anxiety - Treat by gradually increasing time spent away from home and possibly SSRIs
49
Selective Mutism
Child shows persistent failure to speak in social situations where it is expected; speaks fine in other situations at home -Tx with behavioral therapy, speech therapy, SSRIs; not always effective
50
Alphavirus (Togaviridae)
ssRNA(+) virus that are enveloped (via cell membranes) and have an icosahedral capsid; protease sensitive Infection Stages: 1st= After bug bite, multiplies in RE system and rides white cells thru the blood; viremia occurs w/ assoc. B-symptoms 2nd= Virus crosses BBB producing encephalitis accompanied w/ neuronophagia, encephalomalacia, neck pain, confusion Examples are Eastern Equine Encephalitis (least prominent in US) WEE, and Venezuelan EE
51
Flaviviridae
ssRNA (+); enveloped and icosahedral capsid; protease (R) First stage= Viremia and replication in RE system w/ assoc. B-symptomms Second stage= Cross BBB and produce encephalitis Examples include WNV, YFV, Dengue
52
Yellow Fever Virus
Flavivirus that has a second stage involving saddle back (diphasic) fever, necrosis of the liver and kidney (jaundice), and gastric hemorrhages causing RBCs to be destroyed by HCl -Has an effective live-attenuated vaccine, IMPORTED YELLOW FEVER LIKELY THE TOPIC OF THE QUESTION; QUARANTINE PATIENTS WHO HAVE THIS ****CHARACTERISTIC BLACK VOMIT
53
Dengue Fever Virus
Produces a maculopapulaar rash, joint/muscle pain, ocular pain, saddle back fever, and then potentially progresses to hemorrhagic fever and SHOCK Called breakbone fever because it infects BM, this virus consists of 4 serotypes; if infection occurs by 1,3,4 FOLLOWED BY 2, then shock syndrome will occur -Treat hemoconcentration w/ hydration therapy
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Bunyaviridae
ssRNA(-); enveloped (from Golgi) w/ glycoprotein spikes and a helical nucleocapsid; contains many arbovirus serosgroups -RNA exists in 3 segments
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California Bunyavirus serogroup
Found mainly in Mississippi and Ohio river valleys; causes mild headache, N/V, and possible aseptic meningitis *Includes LaCrosse encephalitis seen in WV
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Orthobunyavirus
Can cause Crimean-Congo hemorrhagic fever
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Phlebovirus
Member of the bunyavirus family transmitted by sand fleas and causes headache, fever, maculopapular rash, meningitis, photophobia but results in total immunity if recovered after two years
58
Hantavirus
Bunyavirus acquired from rodent feces and causes Hantavirus Pulmonary Syndrome; assoc. w/ Southwest states ***Treat w/ Ribavirin - Can also cause Korean Hemorrhagic Fever Virus - Assoc. w/ areas of increased rainfall
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Arenaviridae
ssRNA(-) w/ lipid bilayer envelope; helical nucleocapsid; consists of multiple segments connected together Produces old-world and new-world viruses
60
Lymphocytic Choriomeningitis Virus
Spread by the feces of rodents, this virus produces B-symptoms then meningitis ***Can be vertical transmission in pregnant women
61
Lassa Fever
Old world arenavirus that causes hemorrhagic fever, mouth ulcers, skin hemorrhages, and muscle aches -Seen in africa
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Tacribe Complex
New-world arenavirus in South America that causes hemorrhagic fever alongside characteristic petechiae and bleeding into the GI tract, uterus, nasal cavity, and GU tract
63
ECT
Delivery of brief, controlled seizures via electrodes under anesthesia about 2-3/week; used to treat Major Depressive Disorder, Bipolar disorder and thought disorders **DOESNT WORK ON ANXIETY OR PERSONALITY DISORDERS Effects: Increases DA and 5-HT release, decreases metabolic activity in frontal and cingulate cortex, reduces activity in the left dorsolateral PFC, and increases BDNF CIs: Intracranial hemorrhage, strokes, lesions, MI, angina
64
ECT Muscle relaxant
Succinylcholine; only works for 5 mins -Should test for pseudocholinesterase deficiency or proper liver fnxn because this could cause prolonged apnea
65
Methohexital
Rapid action anesthetic used in ECT; second line is etomidate Used ketamine if maximum stimulus reached w/o adequate response
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ADRs of ECT
Postictal disorientation, interictal confusion, memory impairment (retrograde can last really long), dysrhythmia, headache, N/V, moodc changes Limit these by using concentrated, brief pulses, dosing the intensity of the stimulus, and using right-unilateral electrode placement
67
Transcranial Magnetic Stimulation
Non-invasive technique that uses metal coils producing rapidly alternating magnetic fields to generate currents in specific brain regions; often targets the dorsolateral PFC - Have to do way more often the ECT and sessions last 40 mins - Typically less effective than ECT and cannot do if pt. has any metal medical devices implanted
68
Magnetic Stimulation Therapy
Combines the effects of ECT and rTMS w/o the skull impedence and widespread brain stimulation (ECT) or the limited effectiveness of rTMS; done under general anesthesia but has same CIs as rTMS -Becoming an encouraging alternative to ECT
69
DBS
Continuous stimulation of implanted electrodes on the brain being used to treat hyperresistant depression
70
Psychoanalysis
Theory: Object is to make the unconscious, conscious and restore balance b/w the id and super-ego; must work through the internal defense mechanisms the pt. has developed and achieve transference Management: Therapy is "free-flow" and therapist serves as blank slate; failure to meet appt. is seen as resistance
71
Transference
Pt. acts towards the therapist as if they are another important figure in their life bringing to light the unconscious
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Countertransference
The therapist develops an emotional response to the pt. that is merely a reflection of their own, personal experience
73
Humanistic/Person Centered Therapy
Theory: Person can become healthy thru self-realization and on their own given enough time; not defined by any standard or ideal Plan: Therapists are warm and inviting to pts., use open ended statements and empathy, and work to end external idealization w/ happiness coming from the inside -Clients decide how often they will come and they are typically seen as the experts on themselves
74
Behavior Therapy
Theory: Most scientific of the psychotherapies in that if a result cannot be seen or measured, it doesn't matter; popular therapy *especially in lower functioning pts. Plan: Reinforce the desired behaviors usually thru external stimuli; problem focused so therapy may wind up being brief -Tend to avoid using pharmaceuticals and work on the nurturing belief
75
Cognitive Therapy
Theory: Works to change the internal thought processing of an individual; patterns of dysfunctional thinking are what cause psychiatric issues Plan: Highly structured sessions that address specific problems in the pt.; teaches pts. to dispute the negative thoughts that run thru their head - Often involves Homework; use of Socratic dialogue (structured) - Qualifies as evidence based practice; very effective and pts. will use it to apply to many aspects of their life
76
Vascular Type Alzheimers
Risk factors of CVD are the same as in this type of Alzheimer's; typical sx of Alzheimer's however they occur in a stepwise fashion -Will see lacunar infarcts on CT scan
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Lewy Body Dementia
Sx of Parkinson's and dementia; ***ASSOC w/ HALLUCINATIONS and FALLS
78
Delirium definition
MUST HAVE ACUTE ONSET AND INATTENTION -Must also have EITHER disorganized thinking or an altered level of consciousness Risk factors include being a male, over 65, having dementia, vision/hearing loss, polypharmacy, alcohol abuse Tx: Haloperidol; atypicals -Second line would be benzos (usually use if withdrawal etiology)
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Etiology of Delirium
Drugs Electrolyte imbalances Loss of drugs (withdrawal, B12 deficiency, Infection (UTIs, sepsis) Reduced Sensory Input Intracranial tissue (hemorrhage, stroke) Urine retention Major systems (COPD, hypoxia, renal failure)
80
Lewy Body Dementia Treatment
Typically depends on symptoms; Cholinesterase inhibitors(good for Parkinsonism sx) REM Sleep disorder? =>> Clonazepam or Melatonin Hallucinations? =>> Quetiapine IF YOU MUST
81
Neonatal Seizures
- Can be subtle, clonic, tonic, or myoclonic - Due likely to genetics or infection - Cause should always be investigated
82
West Syndrome
"Infantile Spasms" Seizures appear as brief spasms of the head, neck, or limbs and commonly seen w/ a clasp-knife reflex of the arms; head usually drops briefly too and all of this is repetitive -Can be due to cerebral dysformation, tuberous sclerosis, phenylketonuria ***EEEG shows hypsarrhthymia Tx: Refractory to most forms of treatment; ACTH successful
83
Childhood Absence Epilepsy
Presents b/w ages 4-10 and can occur up to 100 times per day - Often confused w/ ADHD due to poor school performance * EEG shows characteristic 3Hz Spike and Wave Tx: Ethosuximate
84
Lennox-Gastaut Syndrome
Presents as a triad of MR, recurring seizures (often atonic), and characteristic EEG -Very hard to treat
85
Febrile Seizures
Generalized seizures that occur w/ fever in children 6months-6yrs; seizures are due to the rapid increase in temp -Risk of epilepsy development increases 10% w/ multiple seizures
86
Benign Focal Epilepsy of Childhood
Simple partial seizures w/ preserved consciousness and the presence of automatisms (including drooling, twitching); at nighttime usually appears global clonic-tonic -Usually disappears by adulthood; carbamazepine is DOC
87
Juvenile Myoclonic Epilepsy
Myoclonic jerks, usually in the morning, that is assoc. w/ family history of epilepsy *IS NOT OUTGROWN -VA is DOC; Carbamazepine makes it worse
88
Frontal Lobe Epilepsy
Bizarre presentation of sx including singing, dancing; easy to miss status epilepticus -Temporal lobe epilepsy is much more common tho and presents w/ strong auras
89
Non-epileptic spells
Frequently a stress response and not consciously controlled, but does not have corresponding irregular EEG activity
90
Optic Neuritis
Common presenting condition of MS that will show afferent pupillary defect, mild pain w/ extraocular movements, and progressive vision loss -Not enough to diagnose on its own though and would not start pt. on preventative tx w/ just this sx
91
Acute Treatment of MS
Methyl-prednisone injection
92
Traditional Tx for MS
IFN-B therapy; can cause fever sx as an ADR ***INEFFECTIVE if pts. smoke because they probably have antibodies -Glatiramir could also be used but causes some pulmonary tightness and is not as effective
93
Teriflunomide
Limits enzyme in pyrimidine synthesis pathway by blocking activation of T and B cells
94
Natalizumab
Monoclonal ab that targets a4-integrin and inhibits white cells from crossing the BBB ADR: PML; must test pts. for JC virus
95
Transverse myelitis
Common presenting sx of MS that shows as hemi-sided weakness, sensory loss, and urinary incontinence due to the presence of a lesion in the SC -Usually does not occur over more than one level
96
Primary Progressive MS
Variant of MS that does not respond to therapies; diagnosis is made in retrospect
97
Neuromyelitis optica
Relapsing inflammatory disease that occurs due to antibodies to the aquaporin 4 chloride channel; can be discovered in a serum IgG test -Presents w/ Sudden vision loss/ocular weakness and urinary incontinence; focal lesion in SC often spans >1 vertebral level **Treated w/ Rituximab which binds to CD20 and induces apoptosis of white cells
98
Complicated Migraine
A migraine w/ an extensive aura that can often mimic a stroke; diagnose thru exclusion of other more serious conditions
99
MAO-B
Incapable of inactivating 5-HT; expressed in platelets so they can store their serotonin
100
Function of Descement's Membrane
Endothelial layer deep to the stromal layer of the cornea that pumps out water to keep the stroma dehydrated =>>Failure to do so causes a milky white appearance of the cornea leading to possible blindness
101
How does a primary HSV infection begin in the eye?
With replication in the epithelial layer of the cornea -Can spread to the stroma causing corneal ulcers which heal poorly
102
Corneal Melting
Severe manifestation of HSV reactivation that occurs when PMNs infiltrate the corneal stroma in response to antigens and further recruit cytokines and macros that exacerbate ulcerations =>>Can lead to destruction of the endothelial membrane and cause excess hydration