Metabolic Encepalopathy Flashcards

1
Q

Metabolic encephalopathy (ME) is associated with these symptoms aside from cognitive and decreased sensorium

A

EPS: Tremors
Seizure
Systemic findings
Skin abnormalities
Ophthalmologic findings

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2
Q

T/F: Metabolic disorders rarely present as an isolated case involving only one system

A

T

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3
Q

Dark red to brown urine reflect excess ________

A

porphyrin excretion

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4
Q

Pathogenesis of ischemic hypoxic encephalopathy (6)

A

Global reduction in CBF -> ischemia
Hypoxia from suffocation
Paralysis of respiratory muscles
CO poisoning
Anoxia -> hippocampus and cerebellum affected

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5
Q

These parts are more resistant to anoxia

A

Brainstem and spinal cord

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5
Q

T/F: watershed infarcts may present if hypoperfusion dominates

Man in the Barrel Syndrome is due to an infarction between what arteries?

A

T

MCA and ACA

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5
Q

T/F: Hyperthermia reduces cerebral metabolic requirements, thus prevents delayed worsening of ME

A

F- hypothermia

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6
Q

T/F: CO poisoning can present in imaging to have symmetric hyperintensity of the globi pallidi, with sparing of the putamen

Initial treatment of CO poisoning

A

T

Inspired oxygen

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7
Q

T/F: extreme altitude causes cerebral edema

Monge disease is aka

A

T

Chronic Mountain sSickness

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8
Q

In DKA, ___ and ___ are elevated in the blood and urine, and there is marked glycosuria

Nonketotic hyperosmolar states have focal signs or symptoms due to previous _________

A

Ketone bodies and B hydroxybutyric acid

Silent cerebrovascular events

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9
Q

This is caused by using aluminum as a substrate for dialysis

This is caused by the cytotoxic edema due to osmotic shifts in water

A

Dialysis encephalopathy
Dialysis disequilibrium syndrome

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10
Q

T/F: Central pontine myelinolysis is a manifestation of hyponatremia

A

F- It’s Osmotic demyelination syndrome (d/t rapid rise of serum osmolality)

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11
Q

Head trauma with damage to the pituitary stalk usually causes ______

A

Central diabetes insipidus

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12
Q

Histopathology found in Wernicke-Korsakoff syndrome

A

Mamillary bodies

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13
Q

This disease has neurological presentations such as length-deepndent, axonal sensorimotor peripheral neuropathy with distal sensory loss

A

Beri-beri

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14
Q

Although rare, this could be caused by intake of isoniazid, hydralazine, or penicillamine

A

Pyridoxine Deficiency

15
Q

This causes Lhermitte’s sign, progressing to gait abnormalities due to combination of sensory ataxia

A

Cobalamin (V12) Deficiency

16
Q

This causes spinocerebellar syndrome, with acanthosis and swollen axons in pathology

A

Vit E Deficiency

17
Q

This disease is associated with chronic alcoholism and involves the demyelination and necrosis of the corpus callosum

A

Marchiafava Bignami Disease

18
Q

T/F: Arsenic causes necrosis of the optic nerves and putamina bilaterally

A

F - methanol

19
Q

This is stored in the reticuloendothelial system and slowly released, causing fatal acute poisoning due to diffuse edema and/or hemorrhagic encephalopathy

A

Arsenic poisoning

20
Q

The Type II syndrome due to this poisoning can cause cardiac failure

A

Organophosphate poisoning

20
Q

This is due to inhibited porphyrin metabolism, causing motor neuropathy commonly involving radial nerve (wrist drop)

A

Inorganic lead poisoning

21
Q

Involves the calcarine cortex, resembling ALS, and causes cognitive impairment (MAD AS A HATTER)

A

Mercury poisoning

22
Q

This poison causes diffuse proximal weakness resembling MG. It also involves postsynaptic (COBROtoxin) and presynaptic (CROtoxin) inhibition of Ach release

A

Snake

23
Q

T/F: Amanita mushrooms block both cholinergic and GABA synapses

A

T