Difference between revisions of "CNS Idiopathic Conditions - Pathology"
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* A seizure is a brain disorder which manifests as paroxysmal cerebral dysrhythmia. | * A seizure is a brain disorder which manifests as paroxysmal cerebral dysrhythmia. | ||
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*** hypoglycaemia | *** hypoglycaemia | ||
*** Hepatic encephalopathy. | *** Hepatic encephalopathy. | ||
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+ | [[Category:Central Nervous System - Idiopathic Pathology]] | ||
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==Pug Dog Encephalitis== | ==Pug Dog Encephalitis== | ||
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* The disease is uniformly fatal. | * The disease is uniformly fatal. | ||
** Corticosterid treatment has no effect. | ** Corticosterid treatment has no effect. | ||
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+ | [[Category:Central Nervous System - Idiopathic Pathology]] | ||
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==Granulomatous Meningoencephalitis== | ==Granulomatous Meningoencephalitis== | ||
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** However, biopsy is required for a definative diagnosis. | ** However, biopsy is required for a definative diagnosis. | ||
* Life span is between 6 months and 1 year from diagnosis. | * Life span is between 6 months and 1 year from diagnosis. | ||
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==Polyneuritis equi== | ==Polyneuritis equi== | ||
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** Abberant parasite migration (e.g. ''Strongylus spp.'') | ** Abberant parasite migration (e.g. ''Strongylus spp.'') | ||
** In endemic areas, ''Sarcocystis neurona'' myelitis (equine protozoal myelitis), rabies and ''rhodococcus equi'' myeloencepahlitis should also be considered. | ** In endemic areas, ''Sarcocystis neurona'' myelitis (equine protozoal myelitis), rabies and ''rhodococcus equi'' myeloencepahlitis should also be considered. | ||
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+ | [[Category:Central Nervous System - Idiopathic Pathology]] |
Revision as of 13:33, 8 March 2011
Idiopathic Epilepsy
- A seizure is a brain disorder which manifests as paroxysmal cerebral dysrhythmia.
- The episode has a sudden onset and ceases spontaneously.
- Seizures tend to recur.
- In epilepsy, individuals appear to have a low seizure threshold.
- This predisposes their neurons to depolarize of their own volition.
- "Idiopathic epilepsy" is said to occur when no other cause of seizuring is apparent.
Pathogenesis
- All seizures arise from a small group of neurons that periodically and spontaneously depolarize.
- In addition to being idiopathic (i.e. low seizure threshold), this sudden, uncontrolled neuronal discharge can occur due to:
- Structural causes
- Neoplasms
- Inflammation
- Trauma
- Biochemical causes
- Hypocalcaemia
- hypoglycaemia
- Hepatic encephalopathy.
- Structural causes
Pug Dog Encephalitis
- A non-infectious central nervous inflammatory disease
- Affects pugs.
- Similar conditions are seen in yorkshire and maltese terriers.
- Officially known as necrotising meningoencephalitis of small dogs.
- Characterised by histological forebrain inflammation and necrosis.
- The disease is uniformly fatal.
- Corticosterid treatment has no effect.
Granulomatous Meningoencephalitis
- A non-infectious central nervous inflammatory disease
- May occur as:
- A disseminated disease
- A focal mass lesion
- A primary occular disease
- Brainstem signs are common, although the forebrain is primarily affected.
- May be incorrectly diagnosed as lymphoma.
- Changes are apparent in the CSF.
- There is usually a mononucloear pleocytosis.
- Sometimes only protein is elveated.
- Diffuse inflammatory changes or a mass lesion will be seen by advanced imaging.
- However, biopsy is required for a definative diagnosis.
- Life span is between 6 months and 1 year from diagnosis.
Polyneuritis equi
- A non-infectious central nervous inflammatory disease
- Polyneuritis equi (PNE) is an uncommon disease which affects mature horses
- Formerly known as 'cauda equina syndrome' or 'cauda equina neuritis'
- May occur as:
- A disease effecting the spinal nerve roots and ganglia of the cauda equina.
- A disease effecting the cranial nerves.
- Cauda equina disease is characterised by progressive loss of anal tone, tail paralysis, urinary and/or faecal incontinence, urine scalding of the hindlimbs, hyperaesthesia and muscle fasciculations over hindquarters.
- If the pelvic nerve roots are also involved, there may be changes in hindlimb gait.
- Cranial nerve signs may be apparent, including signs associated with facial nerve paralysis.
- Changes in the CSF are often non-specific.
- There is usually a moderate mononucloear pleocytosis.
- Protein is usually elveated.
- Histologically, the disease presents as a severe, chronic, destructive lymphocytic and histiocytic polyradiculoneuritis.
- Pathogenesis is not completely understood, but considered to be a T-lymphocyte mediated response to myelin, followed by destruction of myelin and axons by macrophages
- Disease appears similar to:
- Guillain-Barré Syndrome (GBS), an autoimmune demyelinating diease in humans
- Experimental allergic neuritis (EAN) in laboratory animals
- Important differential diagnoses for progressive neurologic signs effecting the bladder, rectum, perineum, tail, penis and hindlimbs in horses include:
- Equine herpesvirus-1 myeloencephalopathy
- Sacral/coccygeal trauma
- Equine motor neuron disease
- Abberant parasite migration (e.g. Strongylus spp.)
- In endemic areas, Sarcocystis neurona myelitis (equine protozoal myelitis), rabies and rhodococcus equi myeloencepahlitis should also be considered.