42. non infectious cns diseases, degenerative cns diseases Flashcards
what are the non infectious cns diseases
granulomatosous meningoencephalomyelitis
necrotizing encephalitis
steroid responsive meningitis arteritis - SRMA
polyradiculoneuritis
granulomatous meningoencephalomyelitis etiology
possibly autoimmune lesions mainly in white matter 3 forms: focal - multifocal - ocular extremely rare in cat
granulomatous meningoencephalomyelitis clinical signs and diagnosis
seizure, cerebellovestibular dysfunction, cervical hyperesthesia
post mortem histology
ante mortem: presumptive diagnosis
CSF: mononuclear pleocytosis, increased protein
CT/MRI: lesions
granulomatous meningoencephalomyelitis therapy, prognosis
life long immunosuppression:
prednisolone, cyclosporine, procarbazine
prognosis: poor, can’t really fix it
necrotizing encephalitis - forms
necrotizing meningoencephalitis - pug encephalitis
necrotizing leukoencephalitis - yorkie encephalitis
necrotizing encephalitis - clinica signs
multiple cavitary necrotizing inflammatory lesions
sign depends on site
often forebrain involvement: seizure, circling, visual deficit with intact PLR, head pressing
necrotizing encephalitis diagnosis, therapy, prognosis
CSF: mononuclear pleocytosis, increased protein
treatment: glucocorticoids
prognosis: grave
steroid responsive meningitis arteritis symptoms
cervical rigidity, hyperesthesia, anorexia, fever
rarely neurologic signs (bleeding into subarachnoid space)
SRMA diagnosis, therapy, prognosis
CSF: neutrophil pleocytosis , elevated IgA, interleukin
long term GCC, sometimes azathriopine
relapse is frequent
prognosis good
polyraduculoneuritis etiology
immune mediated inflammation of nerve radicles and peripheral nerves
coon hound - raccoon
raccoon saliva, other antigens (virus, bac) can also trigger inflammation
polyraduculoneuritis clinical signs
LMN paresis, start at HL, progress to FL in 1-4 days
hyperaesthesia, altered barking sound
polyradiculonephritis therapy, prognosis
supportive therapy, physiotherapy
self resolution after 3-6 weeks
if resp muscles involved - death can occur
degenerative cns disorders - storage disease
storage diseases
abiotrophy: lack of vital substance for life
dystrophy: external cause, nutritional, metabolic, endogenous
storage diseases: error of metabolism
degenerative disorders
- Intervertebral disc disease
- Degenerative myelopathy
- Degenerative lumbosacral stenosis
- Osteoarthritis
- Extradural synovial cyst
- Spondylosis deformans
- Spinal stenosis