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− | ==The Forebrain==
| + | {{toplink |
− | | + | |backcolour = E0EEEE |
− | * The nervous system can be classified functionally to:
| + | |linkpage = Nervous System - Pathology |
− | *# The intercranial structures
| + | |linktext =Nervous System |
− | *# The spinal cord
| + | |maplink = Nervous System (Content Map) - Pathology |
− | *# The peripheral nervous system.
| + | |pagetype =Pathology |
− | * The intercranial structures can be further divided into the '''rostrotentorial''' and '''caudotentorial''' structures.
| + | }} |
− | ** The rostrotentorial structures consist of the cerebral hemispheres, basal nuclei, diencephalon and the rostral portion of the midbrain.
| + | <br> |
− | *** Collectively, these are the forebrain.
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− | * The forebrain is responsible for many functions associated with or requiring consciousness.
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− | ==Clinical Signs==
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− | ===Seizures===
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− | * Seizures are a classical sign of rostrotentorial disease.
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− | ===Altered Mentality/ Behaviour===
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− | * The forebrain contains significant components of the limbic system, which are responsible for emotion.
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− | ** Intercranial disease may therefore give rise to abnormal behaviour and aggression.
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− | ===Circling, Head Pressing, Compulsive Walking=== | |
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− | * These behaviours are associated with unilateral rostrotentorial disease.
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− | * There is a tendency to circle '''towards''' the side of the lesion.
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− | ===Head Aversion===
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− | * Head aversion is also known as head turn.
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− | * Turn is usually towards the side of a unilateral lesion.
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− | ===Menace Deficit===
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− | * There may be a deficit in the menace response on the opposite side to a unilateral lesion.
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− | ** However, the pupillary light reflex (testing optic nerve function) and facial nerve function are found to be normal.
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− | * The lack of a contralateral menace response is associated with poor or absent vision.
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− | ** The menace reflex is a learned response, and requires forebrain processing of visual information.
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− | ** The sign is contralateral because there is significant decussation of the visual fibres at the optic chiasm in animals.
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− | * There may also be a reduction in the medial visual field in the eye ipsilateral to the lesion.
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− | ** This combination of visual field abnormalities is known as '''hemianopia'''.
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− | ===Facial Sensation Deficit===
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− | * There may be a deficit in facial sensation on the side contralateral to a unilateral lesion.
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− | ** This is because CN V sends facial sensory signals to the opposite parietal cortex via the thalamus.
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− | ===Hemiparesis===
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− | * Hemiparesis may be a sign of forebrain disease.
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− | * Many tracts cross at various levels in the CNS, however functional crossover occurs at the level of the causal mesencephalon and rostral pons.
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− | ** Unilateral lesions rostral to this level give contralateral hemipareis.
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− | ** Unilateral lesions caudal to this level give ipsilateral hemiparesis.
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− | ==Differential Diagnosis==
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− | * Remember that the age and breed of the animal are important.
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− | ** Animals present with congenital abnormalities within their first year of life.
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− | ** Young animals are also more predisposed to:
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− | *** Infections - due to their immature immune systems and lack of vaccinations.
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− | *** Intoxications - due to their innate curiosity and propensity to explore with their mouths.
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− | *** Traumatic injury - due to both their curiosity and lack of road sense.
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− | ** Geriatric animals tend to suffer the same kind of neurological problems as other adult animals.
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− | *** Infectious, inflammatory and metabolic disorders.
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− | ** Elderly animals are more likely to suffer from:
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− | *** Neoplasi
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− | *** Vascular problems
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− | *** Degenerative disorders
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− | * It must be determined whether the suspected lesion is due to a systemic disease, or to a structural change in the intracranial nervous system.
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− | ** Structural change can be detected by CT or MRI scanning.
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− | * The following causes must be considered and eliminated.
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− | ===Common Diseases Affecting the Forebrain===
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− | ====Degenerative Diseases====
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− | * Storage diseases
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− | * Cognitive dysfunction syndrome
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− | ====Anomalies====
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− | * Hydrocephalus
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− | * Hydraencephaly
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− | * Lissencephaly
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− | ====Metabolic Diseases====
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− | * Hepatic encephalopathy
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− | ** Most commonly seen with congential liver shunts or with sever liver failure.
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− | * Renal encephalopathy
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− | * Pancreatic disease
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− | * Glucose abnormalities
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− | ** Insulinoma
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− | ** Diabetes Mellitus
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− | * Hypo- and hyper-thyroidism
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− | * Hypoxia, for example due to:
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− | ** Anaemia
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− | ** Cariopulmonary disease
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− | ** Severe URT obstruction
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− | * Hypertension
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− | * Ion inbalances
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− | ** Hypocalcaemia
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− | ** Hypokalaemia
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− | *** For example in chronic renal failure or hyperaldosteronism
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− | ** Hypophosphataemia
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− | ** Hypomagnesaemia
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− | *** E.g. in hepatic lipidosis or re-feeding syndrome.
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− | ====Neoplasia====
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− | * Primary brain tumours
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− | * Metastatic tumours
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− | * Local extension of tumours
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− | ====Nutritional Conditions====
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− | * Thiamine deficiency
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− | ====Infectious Causes====
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− | * Canine distemper
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− | * FIP
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− | * Toxoplasmosis
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− | * Fungal disease
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− | * Rickettsial diseases
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− | * Rock Mountain spotted fever
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− | * Ehrlichia
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− | * Bacterial infections
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− | * Parasitism
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− | ====Trauma====
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− | * Head trauma
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− | ====Toxicity====
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− | * Metranidazole
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− | * Lead
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− | ====Vascular====
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− | * Arteriovenous malformation
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− | * Infarction
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− | * Feline ischaemic encephalopathy
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− | * Haemorrhage
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− | * Hypertension
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− | ==Diagnosis==
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− | * Diagnosis must encompass the following:
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− | ===History===
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− | * Aside from the normal history, there are several very important questions to be asked:
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− | ** Has there been any possible exposure to toxins or trauma?
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− | ** What is the animal's diet?
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− | ** Are the litter mates normal?
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− | ** Are there any specific clinical signs that may relate to a particular diagnosis?
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− | ** E.g. hypersalivation - commonly seens in young animals with portosystemic [[Liver - Anatomy & Physiology|liver]] shunts.
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− | ===Physical Examinations=== | |
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− | * Check for signs of systemic disease.
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− | ** Ocular changes with FIP, toxoplasmosis, FeLV or lysosomal storage diseases.
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− | ** Ascites with with FIP, liver or cardiac disease.
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− | ===Neurological Examination===
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− | * This should include CN examination, postural reactions, spinal reflexes and sensory examination.
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− | ===Blood and Urine Tests===
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− | * Blood tests should include haematology and serum biochemistry.
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− | * These are particularly helpful in the diagnosis of many systemic and especially metabloic conditions.
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− | ===Infectious Disease Tests===
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− | * E.g. FeLV and FIV, toxoplasma [[IgM]] and [[IgG]] tests.
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− | ===CSF Analysis===
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− | * Particularly useful in the diagnosis of:
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− | ** Inflammatory diseases
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− | *** E.g. FIP
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− | ** Lymphoma
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− | ===Imaging===
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− | * Radiographs of the chest and abdomen
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− | * Abdominal ultrasonography
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− | * MRI or CT scans
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− | ** Examine the structure of the brain and determine presence or absence of inflammation or neoplasia.
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− | [[Category:Central Nervous System - Pathology]]
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