MEDICAL CONDITIONS SPINAL: 30 Flashcards

1
Q

Examples of nutritional disorders that can affect the spinal cord

A

-thiamine deficiency
-secondary hyperparatiroidism
-hypervitaminosis A

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2
Q

SPINAL CORD TRAUMA: Many patients will display ………….. of the affected area. Worsening of edema (associated with secondary injury) may lead to …………………. for a short period of ………………….

A

hyperesthesia
progression of neurologic signs
24 to 72 hours

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3
Q

Max amount of CSF collection

A

1 ml per 5Kg

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4
Q

What is the meaning of Xanthocromia in the CSF

A

is a yellow or straw-tinged color of cerebro spinal fluid. From hemorrhage (hemoglobin).

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5
Q

Cutoff values for cellular count in CSF

A

between 0 and 5 WBC x uL
pleyocitosis (>500/uL) should see cloudy

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6
Q

typical location of degenerative myelopathy

A

T3 - L3. Usually exxagerated reflex (upper motor neuron)

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7
Q

percentage of dogs with degenerative mielopathy with loss of patellar reflex

A

10-20%

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8
Q

describe genetic risk factor for degenerative myelopathy

A

missense mutation in SOD1 (superoxide dismutase) gene

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9
Q

pembroke corgis usually have a faster progression of degenerative myelophaty than other breeds T or F

A

False, mean duration of 19 months VS 6-9 (non ambulatory) months other breeds.

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10
Q

signalment+clinical signs of dogs with SRMA

A

medium-large breed, 6-18 months (74% less 1 year).

hyperestesia depression and pyrexia

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11
Q

diagnosis of SRMA

A

marked polymorphonuclear (nondegenerative neutrophils) pleocytosis, in addition to elevated protein and variable red blood cells

elevated IgA serum + CSF

Bacterial culture NEGATIVE!!

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12
Q

SRMA therapy

A

2 mg/Kg/die prednisone, 3/4 weeks before beginning tapering

STOP 6 months after normalization of CSF and resolution clinical signs

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13
Q

granulomatous meningomyelitis: signalment and clinical signs

A

GME can manifest in three clinicopathologic forms: ocular (least common), focal, and multifocal/disseminated (most common form).

It can occur in both large and small breed dogs with a variable age range. The clinical signs reflect the location of the lesion and can occur anywhere in the central nervous system. Pain, seizures and cerebellovestibular dysfunction are seen most commonly.

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14
Q

MUE: explain the acronym and pathologies involved

A

BASED ON HYSTOPATHOLOGY!!!

1) granulomatous meningoencephalitis (GME)
2) necrotizing meningoencephalitis (NME)
3) necrotizing leukocencephalitis (NLE)
4) steroid-responsive meningitis-arteritis (SRMA)

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15
Q

multimodal treatement for MUE

A

cytosine arabinoside and cyclosporine in combination with prednisone as adjunctive thepapy / also procarbazine, leflunomide, mycophenolate

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16
Q

common protozoal meningoencephaloyelitis

A

toxoplasma or neospora

17
Q

most commonly isolated bacterial from discospondylitis

A

staphylococcus and e.coli

18
Q

ethiopatogenesis of discospondylitis

A

hematogenous or lymphatic spread of bacteria

19
Q

performing urine and blood culture is the only diagnostic necessary for discospondylitis diagnosis. T or F

A

F: intervertebral disc aspiration 60% blood + urine combined more than 40%.

20
Q

fibrocartilagineous embolic myelopathy: signalment and clinical signs

A

midsized to large-breed dogs

nonpainful, transient discomfort, which typically resolves rapidly

Neurologic signs are related to the segment of the spinal cord affected L4-S3 (44% to 50%) and T3-L3 (37% to 42%

21
Q

describe the phenomenon spinal shock

A

reduced tone and withdrawal reflex in pelvic limb even with a T3 L3 lesion.

22
Q

All dogs with fibrocartilagineous embolic myelopathy have MRI signs T or F

A

False, 21% had no detectable lesions (MRI timing or severity?)

23
Q

measure for prognosis after fibrocartilagineous embolic myelopathy MRI

A

lesion-to-vertebral length ratio was
≥ 2 had an unsuccessful outcome
≤ 2 100% had a successful outcome