Medical conditions Flashcards
What does the DAMNIT-V pneumonic for spinal cord injury stand for?
Degenerative
Anomalous
Metabolic
Neoplastic
Inflammatory/infectious
Traumatic
Vascular
Describe different spinal cord disorders present based on their onset, progression and symmetry.
What are the two locations for collection of CSF?
- Cerebellomedullary cistern.
- Lumbar subarachnoid space.
No more than 1ml of CSF should be collected per 5 kg of body weight.
In what direction does CSF flow?
Rostrocaudal (ideally CSF collection should be caudal to the suspected lesion).
Are CSF abnormalities specific for certain neurologic conditions?
No. CSF abnormalities are sensitive for detection of disease, but do not definitively delineate the cause.
What is the location of CSF collection from the cerebellomedullary cistern?
Intersection of lines between the external occipital protuberance and spinous process of C2, along the cranial aspect of the wings of the atlas.
What is the site for collection of CSF at the lumbar subarachnoid spacee?
L5/L6 in dogs, L6/L7 in cats.
At this location the cord has typically tapered to the conus medullaris and is less likely to be damaged.
Note: the subarachnoid space rarely extends to the lumbosacral articulation in dogs.
What are the normal cell counts and total protein values for CSF of the dog and cat?
Cell count: 0-5 x 10^9/L
Protein: <25 mg/dL from the cerebellomedullary cistern, <45 mg/dL from the lumbar cistern.
What additional testing may be beneficial on the CSF (aside from protein and cell count)?
- Culture.
- Serology (can compare serum to CSF IgG levels to determine location of infection).
- PCR (may increase the chances of identifying an infectious cause when combined with serology).
Can myelography differentiate between extradural and intradural lesions?
Yes, but can be difficulty to differentiate between intradural-extramedullary and intramedullary lesions.
What is degenerative myelopathy?
An axonopathy that predominantly affects the lateral and ventral funiculi of the white matter of the spinal cord. The axonopathy is accompanied by demyelination and astrogliosis.
What is the most common neurolocalization of patients with degenerative myelopathy?
T3-L3.
Late in the disease may progress to urinary and fecal incontinence, thoracic limb involvement, and rarely LMN of the pelvic limbs.
What is the genetic risk factor for development of degenerative myelopathy?
Missense mutation in the SOD1 gene.
How is degenerative myelopathy diagnosed?
Exclusion of other disorders by imaging, CSF analysis, and the results of testing for the SOD1 mutation.
What treatments are available for degenerative myelopathy?
None. Progression usually results in nonambulatory status by 6-9 months.
What are the types of meningomyelitis?
- Idiopathic.
a. Steroid responsive meningitis arteritis.
b. Granulomatous meningoencephalomyelitis. - Infectious meningomyelitis.
a. Viral meningomyelitis (Canine distemper, FIP)
b. Protozoal.
d. Bacterial.
Are infectious or idiopathic causes of meningomyelitis more common in the cat?
Infectious causes more common in the cat.
Idiopathic and immune mediated disease is more common in the dog.
What are the two forms of SRMA?
- Acute (or classic) form: hyperasthesia, cervical rigidity, stiff gait.
- Chronic form: meningeal fibrosis results in secondary hydrocephalus or ischemia.
Does SRMA more commonly affect old or young dogs?
Young. Age of onset typically 6-18 months.
How is SRMA diagnosed?
CSF, MRI, serum/CSF IgA levels
What can be used to monitor response to therapy when treating SRMA?
Protein C levels.
Elevated IgA levels in both CSF and serum are a common finding, but they remain elevated throughout the disease making them less useful in monitoring response to therapy.
What is the etiopathogenesis of SRMA?
Unknown.