Pathology-Ish Flashcards

(48 cards)

1
Q

Brodmann’s areas

  1. 22
  2. 44, 45
A
  1. Wernicke’s

2. Broca’s

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2
Q

What hemisphere is most often dominant?

A

left

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3
Q

Lesion location of aphasias (most common type of lesion)

  1. Broca
  2. Wernicke
  3. global
  4. conduction
  5. transcortical motor
  6. transcortical sensory
  7. mixed transcortical
  8. anomic
A
  1. Brodmann’s 44, 45 (stroke)
  2. Brodmann’s 22 (stroke)
  3. large area of left hemisphere (stroke)
  4. supra marginal gyrus and arcuate fascicles (occlusion of angular branch of left MCA)
  5. left anterior frontal lobe superior or inferior to Broca’s area (stroke)
  6. between MCA and PCA (stroke, severe hypotension)
  7. between ACA and MCA (stroke, severe hypotension)
  8. anywhere in language area
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4
Q

Lesion location of aphasias

  1. Broca
  2. Wernicke
A
  1. Brodmann’s 44, 45

2. Brodmann’s 22

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5
Q

Gerüstmann syndrome
Sx

location?

A

anomia
alexia, agraphia, acalculia, finger agnosia
right left disorientation

left angular gyrus (area 39)

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6
Q

alexia without agraphia

A

can write, but not read
right homonymous hemianopsia (can’t see right visual field)

location: left medial occipital and temporal lobes involving selenium of corpus callosum

caused by: occlusion of branch of left PCA

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7
Q

Sx of encephalopathy

A
  1. seizures
  2. altered respiration
  3. acute alteration of mental status: delirium, hallucinations, coma, lethargy, stupor; decrease in: attention, memory, orientation, cognition, HIF
  4. altered pupil light reactivity: symmetric and slow
  5. altered ocular motility: roving, absent, dysconjugate
  6. altered motor activity: alteration of strength, tone, reflexes; tremor, myoclonus, asterixis
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8
Q

Sx of encephalopathy

A
  1. seizures
  2. altered respiration
  3. acute alteration of mental status: delirium, hallucinations, coma, lethargy, stupor; decrease in: attention, memory, orientation, cognition, HIF
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9
Q

Wernicke/Korsakoff encephalopathy

Sx, Dx, Tx, population, cause, location of lesions

A

B1 (thiamine) deficiency
ALCOHOL, malnutrition
ENCEPHALOPATHY
Triad: gait ataxia, ophthalmoparesis, confusion
amnesia for recent memories
peripheral neuropathy
Tx: thiamine BEFORE glucose (prevent brain damage)
Dx: clinical (reduced transketolase in blood: not readily available)
location: dorsomedial thalamus, mammillary body, periaqueductal gray
Wet/Dry Beriberi

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10
Q

Niacin deficiency

A

pellagra, encephalopathy
dementia, dermatitis, diarrhea, polyneuropathy
diffuse CNS/PNS involvement

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11
Q

B12 deficiency

  1. causes
  2. Sx
  3. path
  4. Dx
  5. Tx
A

ENCEPHALOPATHY

  1. PERNICIOUS ANEMIA, vegetarian dient, bariatric Sx, sprue, gastric CA, nitrous oxide abuse
  2. pos. ROMBERG, decreased vibration/position sense; Lhermitte’s sign (electric sensation on neck flexion), distal parathesia; spastic gait, confusion/depression/dementia, visual problems, weakness
    anemia: pale, tongue atrophy
  3. demyelination of dorsal columns, corticospinal tract, optic nerves, peripheral nerves, cerebral white matter
  4. microcytic anemia, hyperhsegmented neutrophils, low B12, elevated methylmalonic acid and homocysteine
  5. Tx underlying problem; cyanocobalamin
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12
Q

B12 deficiency

A

/

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13
Q

wet beriberi

A

thiamine deficiency

high output cardiac failure

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14
Q

dry beriberi

A

thiamine deficiency: axonal degeneration

polyneuropathy (lower > upper), decreased pain, loss of ankle/knee reflex

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15
Q

B6 (pyridoxine) deficiency

A

NO encephalopathy

Sx: seizures, polyneuropathy

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16
Q

B complex deficiency

A
TOBACCO/ALCOHOL
lesion: loss of myelination of optic nerve, papillomacular bundle
bilateral
decreased visual acuity: central scotoma
optic disc pallor
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17
Q

hyperglycemic encephalopathy

A

acidosis with high sugar levels, small pupils,

no: brisk reflexes, seizures

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18
Q

hyperglycemic encephalopathy

A

acidosis with high sugar levels, small pupils,

no: brisk reflexes, seizures

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19
Q

hypoxic encephalopathy

A

due to: CARDIAC ARREST, CO poisoning, high altitude sickness, chronic bronchitis
Sx: stupor/coma, seizures, myoclonus, amnesia
damage to: hippocampus, watershed areas, deep cerebellum

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20
Q

CO poisioning

A

cherry red skin with cyanotic hue

Tx: hyperbaric O2

21
Q

high altitude sickness

A

chronic hypoxia with compensated RBC count

22
Q

hepatic encephalopathy

A

due to: ALCOHOLIC LIVER; ACETAMINOPHEN
HIGH AMMONIA
Sx: confusion, seizures, slow EEG with triphasic waves, peripheral asterixis (flapping), myoclonus, BRISK reflexes

23
Q

hepatic encephalopathy

A

HIGH AMMONIA

Sx: confusion, seizures, slow EEG with triphasic waves, peripheral asterixis

24
Q

uremic encephalopathy

A

Sx: seizures, myoclonus, dementia, memory deficits, flapping, DECREASED reflexes, LOW Ca
DYSEQUILIBRIUM syndrome with dialysis: increased intracranial bleeds: SUBDURAL HEMORRHAGE

25
Alzheimer's pathology
loss of cerebral cortical neurons (PARIETAL, TEMPORAL atrophy; less frontal atrophy), neurotic plaques with B-amyloid, neurofibrillary tangles
26
vascular dementia
2nd most common dementia after AD HTN, CAD, PAD, DM same age as AD dementia within 3 months of event
27
frontotemporal dementia
/
28
delirium; dementia 1. onset 2. course 3. duration 4. consciousness 5. attention 6. autonomic function 7. cognition 8. prognosis
1. acute; insidious 2. fluctuations; progressive 3. days/weeks; months/ years 4. altered; not impaired 5. distracted; normal 6. hyperactive; normal 7. confused; impoverished 8. reversible; irreversible
29
delirium
clouding of consciousness with reduced capacity to shift, focus, and sustain attention to environmental stimuli
30
dementia
impairment of intellectual/ cognitive function that interferes with social/ occupational activities
31
Dx of dementia
1. impaired short and long term memory and/or 2. one of the following: impaired judgement, abstract thinking or other disturbance (aphasia, agnosia, etc) 3. disturbances interfere with work/ ADL 4. Sx not occurring only in delirium 5. evidence of organic cause (if no evidence then exclusion of non-organic cause (like depression))
32
Dx of delirium
1. disorientation and memory impairment 2. two of the following: incoherent speech, disturbed sleep/wake cycle, increased/decreased psychomotor activity, or perceptual disturbance (hallucination, misinterpretations) 3. develop over short period of time and fluctuate 4. evidence of organic factor
33
Alzheimer's essential criteria
1. confirmed dementia 2. memory deficits 3. progressive worsening of memory plus one other cognitive function (language, executive function, etc.) 4. no disturbances of consciousness 5. onset: most after 65 (btwn: 40-90) 6. absence of other brain disease other: depression, behavioral changes motor signs, seizure, gait, sensory abnormalities are ABSENT early in course
34
Alzheimer's essential criteria
1. confirmed dementia 2. memory deficits 3. progressive worsening of memory plus one other cognitive function 4. no disturbances of consciousness 5. onset: most after 65 (btwn: 40-90) 6. absence of other brain disease
35
logic behind Alzheimer's Tx
AChE or BuChE inhibitor: increase ACh that is decreased due to atrophied Meynert immunotherapy to clear amyloid
36
memantine
NMDA receptor blocker | Tx: Alzheimer's
37
Dementia with Lewy bodies vs. Parkinson's Tx
dementia responds less well to L-DOPA
38
Parkinson's disease
hypokinetic DA def. ASYMMETRIC onset Sx: bradykinesia, rest tremor, rigidity, postural instability (late, if falling early then something else) other Sx: Stooped, shuffle gait, MASKED face, reduced armswing, micrographic, hypokinetic dysarthria non-motor: depression, anxiety, cognitive impairment ANS: GI (constipation, dysphagia, impaired gastric emptying); low libido; CV: BP regulation; thermoregulatory: profuse sweating; bladder sleep disturbances: REM sleep behavior disorder
39
Progressive Supranuclear Palsy
hypokinetic life expectancy: 10 yrs SYMMETRIC Sx: rigidity, bradykinesia, dysarthria; EARLY GAIT and POSTURAL problems dementia, emotional ASTONISHED face SUPRANUCLEAR GAZE PALSY: impairment of volitional downsize leading to inability to move eyes normal oculocephalic maneuver: eyes can still move when pt. fixes gaze and someone moves their head (not a muscle problem); apraxia of eyelid opening (can open spontaneously but not when asked to do so NO TREMOR BABINSKI sleep problems TAUOPATHY: GLOBOSE type neurofibrillary tangle
40
Multisystems Atrophy
hypokinetic life expectancy: 5-10 yrs Sx: rigidity, bradykinesia, EARLY postural instability, NO TREMOR earlier and more severe ANS dysfunction ataxia, dysarthria, oculomotor abnormalities BABINSKI, SPASTICITY HYPERREFLEXIA, STRIDOR, RAYNAUD's, invountary sighing, postural myoclonus depression NO DEMENTIA GLIAL CYTOPLASMIC INCLUSION bodies that stain for alpha synuclein
41
Huntington's disease
hyperkinetic onset: 35-45 yrs life expectancy: 15-20 yrs chorea (with progression becomes akinetic), dysarthria Behavioral: aggressive, obsessive, irritable, impulsive DEMENTIA eventually: impaired planning, organizing, reasoning, judgment WEIGHT LOSS saccades slow or difficult to initiate; difficulty maintaining gaze
42
Tourette's
hyperkinetic YOUNG, MALE: diminishes sudden movement preceded by urge (can be suppressed temporarily), vocal or sensory tics that change overtime OCD, ADHD
43
Primary Dystonia
AD with penetrance hyperkinetic onset: CHILD ASHKENAZI JEW twisting movement that results in abnormal postures that become fixed starts in LOWER extremities (ankle, foot) DYT1 gent, TORSIN A protein, Glu deletion
44
Wilson's
``` mixed hyper/hypokinetic AR: ATP7B: Cu transporting ATPase onset: 10-20 Sx: hepatic, neurologic, psychiatric KAYSER-FLEISHER rings SUNFLOWER CATARACTS OPALSKI cells increased free Cu, urinary Cu, hepatic Cu decreased: serum ceruloplasmin, serum total Cu ```
45
Wilson's
/
46
juvenile huntington's
parkinsonism rather than chorea right from onset
47
focal dystonia
``` ADULT onset generally sporadic muscles ABOVE waist may be relieved by SENSORY TRICKS may be TASK SPECIFIC ```
48
Types of focal dystonia 1. cranial 2. cervical 3. limb
1. Blepharospasm, oromandibular, laryngeal 2. spasmodic torticollis 3. writer's cramp, musician's dystonia