Extra 3 Flashcards

1
Q

Describe Reye’s syndrome

A

Encephalopathy + liver damage + failure

Due to giving aspirin to kids after flu or chicken pox

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2
Q

Describe mechanism of transverse myelitis

A

Inflammation of neuron across length of spinal cord

Due to infections, MS or idiopathic

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3
Q

S+S, Dx + Tx of transverse myelitis

A

Affects sensory, motor + autonomic bilaterally
LP with increased WBC, MRI
Tx = cause

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4
Q

Describe mechanism of Charcot-marie tooth

A

Auto dom
Progressive hereditary disorder of PNS
Defective protein in myelin sheath
Onion bulb appearance of myelin

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5
Q

S+S of Charcot-marie tooth

A

Muscular atrophy
Weakness + foot drop - hammer toes
Peripheral neuropathy

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6
Q

Dx + Tx of Charcot-marie tooth

A
Dx = electromyography + nerve conduction studies + DNA test 
Tx = supportive
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7
Q

Mechanism + causes of GBS

A

Demyelinating disease of PNS

Develops after infection; campylobacter jejuni, mycoplasma pneumonia, CMV, EBV

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8
Q

S+S of GBS

A

Paraesthesia to touch + vibration
Weakness + loss of reflexes
Damage to cranial nerves
Autonomic - bladder / bowel

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9
Q

Dx + tx of GBS

A

Dx - LP increased protein/ albumin, nerve conduction studies + EMG
Tx = immunosuppressants, plasmophoresis, IVIG

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10
Q

Mechanism of neurofibromatosis

A

Fibrous tumors from nervous system
Type 1 = NF1 - 17
Type 2 = NF2 - 22
Auto dominant

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11
Q

Describe type 1 NF

A

Von Recklinhausen

Fibromas formed from Schwann cells, fibroblasts + immune cells 
Painless, mobile lumps under skin 
Cafe au lait spots 
Lisch nodules on iris 
Risk of seizures + learning difficulties
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12
Q

Describe type 2 NF

A

Brain, spinal cord + cranial nerve tumors
Bilateral acoustic neuroma (tinnitus + hearing loss)
Meningiomas - compress + cause seizures
Risk of cataracts + hamartomas

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13
Q

Describe Von hippel Lindau

A

genetic disease causing tumors in CNS, kidneys, adrenal glands + PNETS
Most commonly haemangioblastoma in retina + brain

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14
Q

Describe spinal muscular atrophy

A

Autosomal recessive

Reduced deep tendon reflexes, flaccid atrophy

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15
Q

Describe glioblastoma

A

Highly malignant brain tumor
Rapidly crosses corpus callosum
Pseudopallitating pattern

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16
Q

Describe meningioma

A

Subdural

Formed of calcifications called pseumomma bodies

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17
Q

Describe oligodendroglioma

A

Typically in frontal lobes (heavily myelinated)

Round nuclei give a fried egg appearance (chicken wire)

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18
Q

Describe haemangioblastoma

A

Commonly in cerebellum

Slow growing, thin capillaries together

19
Q

Describe mechanism of glaucoma

A

group of disease due to raised IOP that damages optic nerve, due to drainage of fluid blocked

20
Q

Describe open angle glaucoma

A

Slow blockage so gradually increasing IOP
Loss of peripheral vision then central
Outer rim atrophy of optic nerve

21
Q

Describe closed angle glaucoma

A

Due to lens being pushed against iris
sudden increase in IOP
Sudden onset eye pain, redness, blurry vision, N/V, haloes

22
Q

Dx + Tx of glaucoma

A
Dx = tonometry of IOP, visual field testing + cupping 
Tx = beta adrenergic receptor antagonists
23
Q

Describe mechanism of IgA nephropathy

A

AKA Berger’s disease
IgA deposits in kidneys - immune complex with IgG
Damage causes haematuria
Presents in childhood after infection of mucosal lining (resp or GI)

24
Q

Describe mechanism of Goodpastures

A

Autoimmune disease
affects lungs + kidneys - hemoptysis + hematuria
Autoantibodies bind to collagen (IgG)
Type 3 hypersensitivity

25
Dx + Tx of goodpastures
Biopsy - antibasement membrane ab | Steroids + immunosuppressants
26
Describe type 1 renal tubular acidosis
Distal - unable to secrete protons | Due to genetic mutation or acquired defect (lithium)
27
Describe type 2 renal tubular acidosis
proximal - unable to reabsorb HCO3- | Due to genetics or part of Fanconi syndrome
28
Describe type 3 renal tubular acidosis
proximal + distal
29
Describe type 4 renal tubular acidosis
Hyperkalaemic acidosis or severe hypovolemia | due to Addisons or SLE/ lithium
30
Tx of renal tubular acidosis
Type 1 + 2 = replenish HCO3- + K+ w/ thiazide + loop diuretics Type 4 = Tx hypoaldosteronism w/ loop diuretics + fludrocortisone
31
Describe mechanism of renal artery stenosis
``` Reduced blood flow so low BP in kidney Kidneys increase systemic BP Renin is increased which causes vasoconstriction + Na+ absorption Can cause bruits String of beads sign ```
32
Mechanism of sarcoidosis
Immune disorder forming nodules around body Non caseating granulomas Large multinucleated cells (Langhans giants) w/ Schaumann bodies or asteroid bodies
33
RF for sarcoidosis
AA | Infection with TB or borrelia burgodorferi
34
Dx of sarcoidosis
Increased Ca + ACE Bronchoalveolar lavage = increased T cells Biopsy is definitive
35
Osteopenia vs osteomalacia
``` Osteopenia = weakened bone, precursor to osteoporosis Osteomalacia = softening bone due to low Vit D + Ca ```
36
Describe causes, S+S, Dx + Tx of encephalitis
95% due to HSV Fever, headache, psych symptoms, seizures, vomiting LP w/ lymphocytosis + increased protein, PCR for HSV tX = acyclovir
37
Types of MND
ALS = LMN signs in arms, UMN signs in legs Primary lateral sclerosis = UMN signs only Progressive muscular atrophy = LMN signs only
38
Dx + Tx of MND
Clinical, electromyography shows decreased action potentials with increased amplitude Tx = riluzole
39
Describe UMN signs
Increased tone Increased reflexes/ clonus Babinski's sign present Weakness is grouped in muscles
40
Describe LMN signs
Decreased tone Atrophy + fasciculations present Decreased reflexes Individual muscles weak
41
Describe Kaposi's sarcoma
Cancer caused by HSV-8 Abnormal blood vessels formed in mouth, nose + throat Biopsy shows spindle cells
42
Describe Nelson's syndrome
Rapid enlargement of ACTH producing adenoma after removal of both adrenal glands (due to Tx for Cushings) Can cause mass effect
43
What heart valve pathology is carcinoid syndrome associated with?
Right sided (TR + PS)
44
S+S of syringomelia
Cape loss of sensation to temp only | Spastic weakness of upper limbs, neuro pain + upgoing plantars