Cerebral Diseases Flashcards

1
Q

What is the Functional Anatomy of Cerebral Syndrome?

A
  • Cerebrum
    • Consciousness, processing of sensory information (touch, pain, proprioception), skilled responses and motor function
    • Facilitates the function of all cranial nerves
  • Thalamus
    • The relay center for all anatomic divisions of the brain
  • Other subcortical brain structures
    • Internal capsule, basal ganglia (caudate, putamen, globus pallidus)
    • Movement, cognition, emotion
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2
Q

What are the clinical signs of cerebral syndrome?

A
  • Gait abnormalities
    • Weakness w/out ataxia
    • Weakness w/ ataxia and deficits
    • Proprioceptive deficits w/ normal strength
  • Conformation
    • Circling (“Big” circles) and compulsive pacing)
    • Head turn, body turn
  • Seizures
  • Contralateral limb and vision deficits
  • Behavior changes (obtundation, head pressing, aggression)
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3
Q

What are some diseases of the Cerebrum?

A
  • Brain tumors
    • primary or metastatic
  • Meningoencephalitis of unknown etiology
    • Granulomatous meningoencephalitis (MUE)
    • Necrotizing meningoencephalitis
  • Steroid-responsive meningitis-arteritis
  • Cerebral vascular accident (stroke)
  • Head trauma
  • Infectious disease
  • Young dogs/cats
    • Lysosomal storage diseases
    • Congenital hydrocephalus
  • Older dogs/cats
    • Senile atrophy
    • Cognitive dysfunction
    • Hypertensive encephalopathy
  • Metabolic - hepatic, renal, hypoglycemic, hypothyroid, hypernatremic
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4
Q

What is Canine Distemper Encephalitis? Signs? Diganostics?

A
  • Affects the Cerebrum, cerebellum, optic tracts, spinal cord
  • Hx - Upper respiratory and GI signs preceding neuro signs
  • Causes:
    • blindness
    • seizures
    • central vestibular
    • cerebellar
    • spinal cord
    • myoclonus
    • Hyperkeratosis of foot pads
    • Gold-medallion lesions of retina
  • Dx:
    • PCR - urine, conjunctival, pharyngeal, nasal, blood
    • CSF - mononuclear pleocytosis and increased CDV IgG
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5
Q

What is Steroid-Responsive Meningitis arteritis (SRMA)?

A
  • “aseptic meningitis”
  • # 2 inflammatory CNS disease
  • Young 8-18mo, large breed dogs
  • Signs:
    • neck pain
    • fever
    • stiffness
    • ataxia
  • Diagnostics:
    • CBC - leukocytosis with left shift
    • CSF - marked neutorphilic pleocytosis
    • Positive response to steroids
  • Tx - immunosuppressive prednisone (2mg/kg/day)
    • going to be 4 - 5 months
  • Beagle Pain syndrome
    • Necrotizing polyarteritis
    • Frequently recurrent
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6
Q

What is Bacterial Meningitis / Encephalitis? Signs? etiology?

A
  • Peracute, acute or gradual onset (2-3wks)
    • Peracute - deteriorate so quickly referral is generally recommended and survival is low
  • Signs:
    • Lethargy
    • reluctance to walk
    • anorexia
    • neck pain
    • hyperthermia
    • bradycardia
    • depression
    • seizures
  • Dx:
    • Fundic exam (optic neuritis)
    • elevated WBC
    • CSF tap + culture - neutrophilic pleocytosis
  • Tx:
    • Antibiotics that cross BBB (fluoroquinolones, 3rd gen cephalosporins, trimethoprim0sulfa, chloramphenicol, doxy, macrolides)
    • Steroids for first 24-48hr at anti-inflammatory dose
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7
Q

What is Fungal Meningoencephalitis? Causes? signs? Dx?

A
  • Causes:
    • Cryptococcus
    • Histoplasmosis
    • Blastomycosis
  • Signs consistent with bacterial meningitis
  • Often a component of systemic disease
  • Dx:
    • CSF
    • Urine antigen testing
    • serology
    • Fundic exam - fungal plaques
  • Tx:
    • Fluconazole, Itraconazole
    • Amphotericin B
    • Posaconazole, Voriconazole (cats)
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8
Q

What is Meningoencephalitis of unknown etiology (MUE or MUO)?

A
  • Granulomatous Meningoencephalitis (GME)
    • Ocular - acute or subacute vision loss
    • focal - mass lesion
    • disseminated - multifocal signs
  • Necrotizing Meningoencephalitides (NME)
    • Pug dog encephalitis - uncommon
      • acute and cronic forms
      • seizures, abnormal behavior, gait, posture, circling, head tilt, head pressing, and blindness
    • yorkshire terrier necrotizing encephalitis
  • Nonsuppurative, inflammatory disease
  • Affects the cerebrum, cerebellum, Ponse, Medulla, and spinal cord
  • Diffuse of coalescing lesions
  • Common etiology:
    • toy breeds
    • females
    • 1-8yrs
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9
Q

How is MUO (GME/NME/PDE) diagnosed? Tx?

A
  • Dx:
    • Suspicion based on clinical signs and signalment
    • CT, MI
    • CSF - mononuclear to mixed pleocytosis, elevated protein
  • Tx:
    • Prednisone
    • Cyclosporine
    • Cytosine arabinoside
    • Leflunomide, Mycophenolate
    • Antiepileptics (PDE)
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10
Q

What are strokes?

A
  • Cerebrovascular accident
  • Peracute to acute onset with nonprogressive signs after 24 hours
  • May be primary or secondary
    • Hyperadrenocorticism, Protein-losing nephropathy, Feline cardiomyopathies, Immune mediated hemolytic anemia
    • thrombocytopenia, coagulopathy
    • Tumors
  • Types: Ischemic (most common) and hemorhagic (<20)
  • Locations: Cerbral, thalamic, Cerebellar (~50%), Brainstem
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11
Q

What is the prognosis of a stroke? management?

A
  • Outcome dependent on etiology
  • 50 - 75% have good long-term outcomes
  • Recurrent events in up to 30%
  • Management:
    • Mannitol or hypertonic saline in acute phase if high intracranial pressure
    • Anti-epileptic drugs if seizures
    • Treat underlying disease
    • Supportive
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12
Q

What is a transient ischemic attack

A

brief loss of function but with recovery in <24hrs

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13
Q

What is Chiari-like Malformation? Clinical signs? Tx?

A
  • Caudal Occipital Malformation Syndrome (COMS)
  • Syringohydromyelia
    • abnormal spinal cord fluid accumulation
    • complex pathogenesis
  • Clinical signs
    • Spinal pain, paresis, ataxia
    • facial scratching or rubbing
    • Resentment of touching, grooming
    • LMN signs to thoracic limbs
  • Tx:
    • Medical - corticosteroids, carbonic anhydrase inhibitors, analgesics
    • Surgery - enlargement of foramen magnum and caudal fossa
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14
Q

What findings are seen in an MRI on a patient with Chiari-like malformation?

A
  • Small foramen magnum
  • Small caudal fossa volume
  • Cerebellar herniation
  • Hydrocephalus
  • Syringohyromyelia
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15
Q

What are some Metabolic Encephalopathies? what neurological issues do they cause?

A
  • Uremic encephalopathy
    • Long-standing chronic renal failure
    • Hypertension (common in CKD), hyperparathyroidism, acidemia
  • Hepatic encephalopathy
    • Acute or chronic liver disease
    • Neurodepressive
    • Ammonia, Benzodiazepine-like substances, GABA (Portosystemic shunts)
  • Hypothyroidism
    • Myxedema stupor or coma
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16
Q

What are lysosomal storage diseases? Signs? Dx? Tx?

A
  • Hereditary disease
    • Defect in lysosomal pathway
    • Accumulation of intermediate metabolite
    • resultant cell death
  • Clinical syndromes
    • Central and/or peripheral nevous system disease
    • Hepatomegaly
    • Skeletal abnormalities
    • Young onset
  • Dx:
    • Clinical (presumptive)
    • MRI, CT
    • Genetic screening
    • Urine metabolite screen (limited)
    • Histopathology
  • Tx:
    • None
    • acetyl-carnitine (ceroid lipofuscinosis)
17
Q

What are some common CNS Neoplasias?

A
  • Meningioma
    • most common in dogs and cats (multiple lesions)
    • occur peripherally, midline, tentorial, ventral, or lateral to the brainstem, within ventricles
  • Astrocytoma
    • equal occurrence in dogs
    • variable malignancy
    • increased risk in brachycephalics
  • Oligodendroglioma
    • more in males, brachycephalics
    • more often frontal lobes
  • Choroid plexus tumor
    • arise in 4th ventrible, can occur in lateral and 3rd ventricles
  • Ependymal tumors, gangliocytomas, medulloblastomas, etc.