|
|
(4 intermediate revisions by 2 users not shown) |
Line 1: |
Line 1: |
− | {{review}}
| + | #redirect[[:Category: Central Nervous System - Idiopathic Pathology]] |
− | | |
− | {{toplink
| |
− | |backcolour = E0EEEE
| |
− | |linkpage = Nervous System - Pathology
| |
− | |linktext =Nervous System
| |
− | |maplink = Nervous System (Content Map) - Pathology
| |
− | |pagetype =Pathology
| |
− | }}
| |
− | <br>
| |
− | ==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.
| |
− | | |
− | ==Pug Dog Encephalitis==
| |
− | | |
− | * A non-infectious [[CNS Inflammation - Pathology|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 [[CNS Inflammation - Pathology|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 [[CNS Inflammation - Pathology|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 not completely understood, but considered to be caused by 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.
| |